2-Methoxyethanol and its acetate (2-Methoxyethyl acetate)
The consolidated GB Cosmetics Regulation lists this record in Annex II.
Regulatory decision and full conditions
- Status
- Prohibited
- Legal role
- Binding rule
- Regulatory summary
- The consolidated GB Cosmetics Regulation lists this record in Annex II.
- Conditions and restrictions
- A prohibition entry may contain no separate condition text because the regulatory outcome is the prohibition itself. Open the cited source and apply the market-wide requirements below.
Substance identity
- Official source name
- 2-Methoxyethanol and its acetate (2-Methoxyethyl acetate)
- CAS
- 109-86-4; 110-49-6
- EC
- 203-713-7; 203-772-9
- Identity mapping
- cas_number
- Linked ingredient
- METHOXYETHANOL
Linked CosIng identity data
Names and aliases
CosIng description: Ethylene Glycol Monomethyl Ether Ethanol, 2-Methoxy- Ethylene glycol methyl ether Ethylene Glycol Monomethyl Ether
EU inventory restriction note: II/665 CMR1b (Reprotoxic 1B)
Recorded cosmetic function: SOLVENT, VISCOSITY CONTROLLING
Function pages:SOLVENT, VISCOSITY CONTROLLING
View the complete ingredient profileCross-market snapshot for this identity
Exact linked records currently present in this site. An absent market means no imported exact match, not permission to use the substance.
European Union
1 linked record
Open supporting recordGreat Britain
Current record1 linked record
Open supporting recordCanada
2 linked records
Open supporting recordNew Zealand
2 linked records
Open supporting recordASEAN
2 linked records
Open supporting recordChina
1 linked record · 1 with specific conditions
Open supporting recordSouth Korea
2 linked records
Open supporting recordBrazil
2 linked records · 2 with specific conditions
Open supporting recordIndia
1 linked record · 1 with specific conditions
Open supporting recordSaudi Arabia
2 linked records
Open supporting recordVerified chemistry for CAS 109-86-4
2-Methoxyethanol
2-methoxyethanol is a hydroxyether that is ethanol substituted by a methoxy group at position 2. It has a role as a solvent and a protic solvent. — ChEBI
- IUPAC name
- 2-methoxyethanol
- Molecular formula
- C3H8O2
- Molecular weight
- 76.09 g/mol
- Exact mass
- 76.052429494 Da
- Monoisotopic mass
- 76.052429494 Da
- XLogP3
- -0.8
- Topological polar surface area
- 29.5 Ų
- Molecular complexity
- 14.0
- Formal charge
- 0
- Hydrogen-bond donors
- 1
- Hydrogen-bond acceptors
- 2
- Rotatable bonds
- 2
- Heavy atoms
- 5
- Covalent units
- 1
Names and synonyms reported to PubChem
16 more reported names
External database identifiers
- ChEBI:CHEBI:46790
- ChEBI:CHEBI:53449
- ChEMBL:CHEMBL444144
- EPA DTXSID:DTXSID5024182
- PubMed:32979392
- PubMed:32418910
- PubMed:29205417
- PubMed:23039368
- PubMed:22953186
- PubMed:22939339
- PubMed:22897679
- PubMed:22887830
- PubMed:22580533
- PubMed:22565476
- PubMed:22472325
- PubMed:22457661
Advanced structure statistics
- Defined atom stereocentres
- 0
- Undefined atom stereocentres
- 0
- Defined bond stereocentres
- 0
- Undefined bond stereocentres
- 0
- 3D pharmacophore features
- 3
- 3D rings
- 0
- 3D hydrophobes
- 0
- 3D acceptor features
- 2
- 3D donor features
- 1
- 3D anionic centres
- 0
- 3D cationic centres
- 0
- 3D conformers
- 8
- Effective 3D rotors
- 2.0
Machine-readable structure identifiers
- SMILES
COCCO- InChI
InChI=1S/C3H8O2/c1-5-3-2-4/h4H,2-3H2,1H3- InChIKey
XNWFRZJHXBZDAG-UHFFFAOYSA-N
Evidence from additional scientific databases
NIH PubChem PUG-View
Attributed physical-property, hazard, environmental and use annotations.
- Autoignition Temperature: 551 °F (USCG, 1999) Source: CAMEO Chemicals
- Autoignition Temperature: 285 °C Source: Hazardous Substances Data Bank (HSDB)
- Autoignition Temperature: 285 °C Source: ILO-WHO International Chemical Safety Cards (ICSCs)
- Boiling Point: 257 °F at 768 mmHg (NTP, 1992) Source: CAMEO Chemicals
- Boiling Point: 124.1 °C Source: DrugBank
- Boiling Point: 124.1 °C Source: Hazardous Substances Data Bank (HSDB)
- Boiling Point: 125 °C Source: ILO-WHO International Chemical Safety Cards (ICSCs)
- Boiling Point: 256 °F Source: Occupational Safety and Health Administration (OSHA)
- Boiling Point: 124.5 °C @760 [mm Hg] Source: PAC Chemical Database, U.S. Department of Energy
- Boiling Point: 256 °F Source: The National Institute for Occupational Safety and Health (NIOSH)
- Color/Form: Colorless liquid Source: Hazardous Substances Data Bank (HSDB)
- Density: 0.966 at 68 °F (USCG, 1999) - Less dense than water; will float Source: CAMEO Chemicals
- Density: 0.9647 g/cu cm at 20 °C Source: Hazardous Substances Data Bank (HSDB)
- Density: Bulk density: 8.0 lb/gal Source: Hazardous Substances Data Bank (HSDB)
- Density: Relative density (water = 1): 0.96 Source: ILO-WHO International Chemical Safety Cards (ICSCs)
- Density: 0.96 Source: Occupational Safety and Health Administration (OSHA)
- Density: 1.4 @ 20°C Source: PAC Chemical Database, U.S. Department of Energy
- Density: 0.96 Source: The National Institute for Occupational Safety and Health (NIOSH)
- pKa: 14.8 (at 25 °C) Source: DrugBank
- Dissociation Constants: pKa = 14.8 at 25 °C Source: Hazardous Substances Data Bank (HSDB)
- Flash Point: 107 °F (NTP, 1992) Source: CAMEO Chemicals
- Flash Point: 41.7 °C Source: Haz-Map, Information on Hazardous Chemicals and Occupational Diseases
- Flash Point: 42 °C closed cup Source: Hazardous Substances Data Bank (HSDB)
- Flash Point: 120 °C open cup Source: Hazardous Substances Data Bank (HSDB)
- Flash Point: Flash point 40 °C (104 °F) - closed cup Source: Hazardous Substances Data Bank (HSDB)
- Flash Point: 39 °C c.c. Source: ILO-WHO International Chemical Safety Cards (ICSCs)
- Flash Point: 102 °F Source: Occupational Safety and Health Administration (OSHA)
- Flash Point: 102 °F Source: The National Institute for Occupational Safety and Health (NIOSH)
- LogP: -0.77 Source: DrugBank
- LogP: log Kow = -0.77 Source: Hazardous Substances Data Bank (HSDB)
- LogP: -0.503 Source: ILO-WHO International Chemical Safety Cards (ICSCs)
- Melting Point: -121.2 °F (NTP, 1992) Source: CAMEO Chemicals
- Melting Point: -85.1 °C Source: DrugBank
- Melting Point: -85.1 °C Source: Hazardous Substances Data Bank (HSDB)
- Melting Point: -85 °C Source: ILO-WHO International Chemical Safety Cards (ICSCs)
- Melting Point: -121 °F Source: Occupational Safety and Health Administration (OSHA)
- Melting Point: -86.5 °C Source: PAC Chemical Database, U.S. Department of Energy
- Melting Point: -121 °F Source: The National Institute for Occupational Safety and Health (NIOSH)
- Odor: Mild agreeable odor Source: Hazardous Substances Data Bank (HSDB)
- Odor: Ether-like odor Source: Hazardous Substances Data Bank (HSDB)
- Physical Description: Ethylene glycol monomethyl ether appears as a clear colorless liquid. Flash point of 110 °F. Less dense than water. Vapors are heavier than air. Source: CAMEO Chemicals
- Physical Description: Wet Solid; Liquid Source: EPA Chemical Data Reporting (CDR)
- Physical Description: Colorless liquid with a mild, ether-like odor; [NIOSH] Source: Haz-Map, Information on Hazardous Chemicals and Occupational Diseases
- Physical Description: COLOURLESS LIQUID WITH CHARACTERISTIC ODOUR. Source: ILO-WHO International Chemical Safety Cards (ICSCs)
- Physical Description: Colorless liquid with a mild, ether-like odor. Source: Occupational Safety and Health Administration (OSHA)
- Physical Description: Colorless liquid with a mild, ether-like odor. Source: The National Institute for Occupational Safety and Health (NIOSH)
- Refractive Index: Index of refraction: 1.4024 at 20 °C/D Source: Hazardous Substances Data Bank (HSDB)
- Solubility: greater than or equal to 100 mg/mL at 70 °F (NTP, 1992) Source: CAMEO Chemicals
- Solubility: 1000000 mg/L (at 25 °C) Source: DrugBank
- Solubility: Miscible with water Source: Hazardous Substances Data Bank (HSDB)
- Solubility: Miscible with alcohol, ether, acetone, dimethylformamide Source: Hazardous Substances Data Bank (HSDB)
- Solubility: Miscible with hydrocarbons, alcohols, ketones, glycols Source: Hazardous Substances Data Bank (HSDB)
- Solubility: Solubility in water: miscible Source: ILO-WHO International Chemical Safety Cards (ICSCs)
- Solubility: Miscible Source: The National Institute for Occupational Safety and Health (NIOSH)
- Vapor Pressure: 6.2 mmHg at 68 °F ; 10 mmHg at 71.6 °F (NTP, 1992) Source: CAMEO Chemicals
- Vapor Pressure: 9.5 [mmHg] Source: Haz-Map, Information on Hazardous Chemicals and Occupational Diseases
- Vapor Pressure: 9.5 mm Hg at 25 °C Source: Hazardous Substances Data Bank (HSDB)
- Vapor Pressure: Vapor pressure, kPa at 20 °C: 0.83 Source: ILO-WHO International Chemical Safety Cards (ICSCs)
- Vapor Pressure: 6 mmHg Source: Occupational Safety and Health Administration (OSHA)
- Vapor Pressure: 9.5 [mm Hg] @25 °C Source: PAC Chemical Database, U.S. Department of Energy
- Vapor Pressure: 6 mmHg Source: The National Institute for Occupational Safety and Health (NIOSH)
- Carcinogen Classification: No indication of carcinogenicity to humans (not listed by IARC). Source: Toxin and Toxin Target Database (T3DB)
- Exposure Routes: The substance can be absorbed into the body by inhalation, through the skin and by ingestion. Source: ILO-WHO International Chemical Safety Cards (ICSCs)
- Exposure Routes: inhalation, skin absorption, ingestion, skin and/or eye contact Source: The National Institute for Occupational Safety and Health (NIOSH)
- First Aid: EYES: First check the victim for contact lenses and remove if present. Flush victim's eyes with water or normal saline solution for 20 to 30 minutes while simultaneously calling a hospital or poison control center. Do not put any ointments, oils, or medication in the victim's eyes without specific instructions from a physician. IMMEDIATELY transport the victim after flushing eyes to a hospital even if no symptoms (such as redness or irritation) develop.; SKIN: IMMEDIATELY flood affected skin with water while removing and isolating all contaminated clothing. Gently wash all affected skin areas thoroughly with soap and water. If symptoms such as redness or irritation develop, IMMEDIATELY call a physician and be prepared to transport the victim to a hospital for treatment.; INHALATION: IMMEDIATELY leave the contaminated area; take deep breaths of fresh air. If symptoms (such as wheezing, coughing, shortness of breath, or burning in the mouth, throat, or chest) develop, call a physician and be prepared to transport the victim to a hospital. Provide proper respiratory protection to rescuers entering an unknown atmosphere. Whenever possible, Self-Contained Breathing Apparatus (SCBA) shou Source: CAMEO Chemicals
- ERG2024, Guide 127 (Ethylene glycol monomethyl ether): General First Aid:; · Call 911 or emergency medical service.; · Ensure that medical personnel are aware of the material(s) involved, take precautions to protect themselves and avoid contamination.; · Move victim to fresh air if it can be done safely.; · Administer oxygen if breathing is difficult.; · If victim is not breathing:; -- DO NOT perform mouth-to-mouth resuscitation; the victim may have ingested or inhaled the substance.; -- If equipped and pulse detected, wash face and mouth, then give artificial respiration using a proper respiratory medical device (bag-valve mask, pocket mask equipped with a one-way valve or other device).; -- If no pulse detected or no respiratory medical device available, provide continuous compressions. Conduct a pulse check every two minutes or monitor for any signs of spontaneous respirations.; · Remove and isolate contaminated clothing and shoes.; · For minor skin contact, avoid spreading material on unaffected skin.; · In case of contact with substance, remove immediately by flushing skin or eyes with running water for at least 20 minutes.; · For severe burns, immediate medical attention is required.; · Effects of exposure (inhalation, ingestion, Source: Emergency Response Guidebook (ERG)
- First Aid: (General first aid procedures); Eye: Irrigate immediately - If this chemical contacts the eyes, immediately wash (irrigate) the eyes with large amounts of water, occasionally lifting the lower and upper lids. Get medical attention immediately.; Skin: Water flush promptly - If this chemical contacts the skin, flush the contaminated skin with water promptly. If this chemical penetrates the clothing, immediately remove the clothing and flush the skin with water promptly. If irritation persists after washing, get medical attention.; Breathing: Respiratory support; Swallow: Medical attention immediately - If this chemical has been swallowed, get medical attention immediately. Source: The National Institute for Occupational Safety and Health (NIOSH)
- Signal: Danger Source: Regulation (EC) No 1272/2008 of the European Parliament and of the Council
- GHS Hazard Statements: H226: Flammable liquid and vapor [Warning Flammable liquids]; H302: Harmful if swallowed [Warning Acute toxicity, oral]; H312: Harmful in contact with skin [Warning Acute toxicity, dermal]; H332: Harmful if inhaled [Warning Acute toxicity, inhalation]; H360FD: May damage fertility; May damage the unborn child [Danger Reproductive toxicity] Source: Regulation (EC) No 1272/2008 of the European Parliament and of the Council
- Precautionary Statement Codes: P203, P210, P233, P240, P241, P242, P243, P261, P264, P270, P271, P280, P301+P317, P302+P352, P303+P361+P353, P304+P340, P317, P318, P321, P330, P362+P364, P370+P378, P403+P235, P405, and P501 (click each P-code to see the statement) Source: Regulation (EC) No 1272/2008 of the European Parliament and of the Council
- Signal: Danger Source: European Chemicals Agency (ECHA)
- GHS Hazard Statements: H226 (97%): Flammable liquid and vapor [Warning Flammable liquids]; H302+H312+H332 (41.2%): Harmful if swallowed, in contact with skin or if inhaled [Warning Acute toxicity, oral; acute toxicity, dermal; acute toxicity, inhalation]; H302 (96.9%): Harmful if swallowed [Warning Acute toxicity, oral]; H312 (97%): Harmful in contact with skin [Warning Acute toxicity, dermal]; H332 (94.5%): Harmful if inhaled [Warning Acute toxicity, inhalation]; H360 (93.8%): May damage fertility or the unborn child [Danger Reproductive toxicity]; H370 (10.6%): Causes damage to organs [Danger Specific target organ toxicity, single exposure]; H373 (14.1%): May causes damage to organs through prolonged or repeated exposure [Warning Specific target organ toxicity, repeated exposure] Source: European Chemicals Agency (ECHA)
- Precautionary Statement Codes: P203, P210, P233, P240, P241, P242, P243, P260, P261, P264, P270, P271, P280, P301+P317, P302+P352, P303+P361+P353, P304+P340, P308+P316, P317, P318, P319, P321, P330, P362+P364, P370+P378, P403+P235, P405, and P501 (click each P-code to see the statement) Source: European Chemicals Agency (ECHA)
- ECHA C&L Notifications Summary: Aggregated GHS information provided per 1202 reports by companies from 34 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.; Information may vary between notifications depending on impurities, additives, and other factors. The percentage value in parenthesis indicates the notified classification ratio from companies that provide hazard codes. Only hazard codes with percentage values above 10% are shown. For more detailed information, please visit ECHA C&L website. Source: European Chemicals Agency (ECHA)
- Signal: Danger Source: NITE-CMC
- GHS Hazard Statements: H226: Flammable liquid and vapor [Warning Flammable liquids]; H312: Harmful in contact with skin [Warning Acute toxicity, dermal]; H332: Harmful if inhaled [Warning Acute toxicity, inhalation]; H335: May cause respiratory irritation [Warning Specific target organ toxicity, single exposure; Respiratory tract irritation]; H336: May cause drowsiness or dizziness [Warning Specific target organ toxicity, single exposure; Narcotic effects]; H360: May damage fertility or the unborn child [Danger Reproductive toxicity]; H370: Causes damage to organs [Danger Specific target organ toxicity, single exposure]; H372: Causes damage to organs through prolonged or repeated exposure [Danger Specific target organ toxicity, repeated exposure] Source: NITE-CMC
- Precautionary Statement Codes: P203, P210, P233, P240, P241, P242, P243, P260, P261, P264, P270, P271, P280, P302+P352, P303+P361+P353, P304+P340, P308+P316, P317, P318, P319, P321, P362+P364, P370+P378, P403+P233, P403+P235, P405, and P501 (click each P-code to see the statement) Source: NITE-CMC
- GHS Hazard Statements: H226: Flammable liquid and vapor [Warning Flammable liquids]; H312: Harmful in contact with skin [Warning Acute toxicity, dermal]; H331: Toxic if inhaled [Danger Acute toxicity, inhalation]; H360: May damage fertility or the unborn child [Danger Reproductive toxicity]; H370: Causes damage to organs [Danger Specific target organ toxicity, single exposure]; H372: Causes damage to organs through prolonged or repeated exposure [Danger Specific target organ toxicity, repeated exposure] Source: NITE-CMC
- Precautionary Statement Codes: P203, P210, P233, P240, P241, P242, P243, P260, P261, P264, P270, P271, P280, P302+P352, P303+P361+P353, P304+P340, P308+P316, P316, P317, P318, P319, P321, P362+P364, P370+P378, P403+P233, P403+P235, P405, and P501 (click each P-code to see the statement) Source: NITE-CMC
- Target Organs: Reproductive Source: EPA Integrated Risk Information System (IRIS)
- Target Organs: Eyes, respiratory system, central nervous system, blood, kidneys, reproductive system, hematopoietic system Source: The National Institute for Occupational Safety and Health (NIOSH)
- Toxicity Summary: IDENTIFICATION AND USE: 2-Methoxyethanol (2-ME) is a colorless liquid with ether-like odor. It is used as a solvent for cellulose acetate, natural and synthetic resins, some alcohol-soluble dyes; in nail polishes, quick-drying varnishes and enamels, and wood stains. It is also used as a as a jet fuel de-icer. HUMAN EXPOSURE AND TOXICITY: The substance is mildly irritating to the eyes and respiratory tract and may cause effects on the central nervous system, blood, bone marrow, kidneys and liver. Exposure at high levels could cause unconsciousness. The liquid defats the skin. Two non-fatal cases of poisoning by consuming 100 mL 2-ME in men aged 41 and 23 were reported. In addition to agitation and confusion, the predominant clinical features were nausea, cyanosis, hyperventilation, slight tachycardia, and metabolic acidosis. In one patient there were suggestions of moderate kidney failure. No evidence of liver damage was found and both patients recovered within 4 weeks. Chronic poisonings from vapors lead to toxic encephalopathy and evidence of bone marrow depression without hemolysis. Lung, kidney and liver changes have been observed. It was found that individuals exposed in utero Source: Hazardous Substances Data Bank (HSDB)
- Environmental Bioconcentration: An estimated BCF of 3 was calculated in fish for 2-methyoxyethanol(SRC), using a log Kow of -0.77(1) and a regression-derived equation(2). According to a classification scheme(3), this BCF suggests the potential for bioconcentration in aquatic organisms is low(SRC). Source: Hazardous Substances Data Bank (HSDB)
- Environmental Fate: TERRESTRIAL FATE: Based on a classification scheme(1), an estimated Koc value of 1(SRC), determined from a log Kow of -0.77(2) and a regression-derived equation(3), indicates that 2-methoxyethanol is expected to have very high mobility in soil(SRC). Volatilization of 2-methoxyethanol from moist soil surfaces is expected to be an environmental fate process(SRC) given a Henry's Law constant of 3.3X10-7 atm-cu m/mole(4). The potential for volatilization of 2-methoxyethanol from dry soil surfaces may exist(SRC) based upon a vapor pressure of 9.5 mm Hg(5). Utilizing the Japanese MITI test, 83% of the Theoretical BOD was reached in 2 weeks(6) indicating that biodegradation is an important environmental fate process in soil(SRC). Source: Hazardous Substances Data Bank (HSDB)
- Environmental Fate: AQUATIC FATE: Based on a classification scheme(1), an estimated Koc value of 1(SRC), determined from a log Kow of -0.77(2) and a regression-derived equation(3), indicates that 2-methoxyethanol is not expected to adsorb to suspended solids and sediment(SRC). Volatilization from water surfaces may occur(4) based upon a Henry's Law constant of 3.3X10-7 atm-cu m/mole(5). Using this Henry's Law constant and an estimation method(3), volatilization half-lives for a model river and model lake are 97 days and 700 days, respectively(SRC). According to a classification scheme(6), an estimated BCF of 3(SRC), from its log Kow(2) and a regression-derived equation(3), suggests the potential for bioconcentration in aquatic organisms is low(SRC). Utilizing the Japanese MITI test, 83% of the Theoretical BOD was reached in 2 weeks(7) indicating that biodegradation is an important environmental fate process in water(SRC). Source: Hazardous Substances Data Bank (HSDB)
- Environmental Fate: ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), 2-methoxyethanol, which has a vapor pressure of 9.5 mm Hg at 25 °C(2), is expected to exist solely as a vapor in the ambient atmosphere. Vapor-phase 2-methoxyethanol is degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals(SRC); the half-life for this reaction in air is estimated to be 31 hours(SRC), calculated from its rate constant of 1.25X10-11 cu cm/molecule-sec at 25 °C(3). 2-Methoxyethanol does not contain chromophores that absorb at wavelengths >290 nm(4) and, therefore, is not expected to be susceptible to direct photolysis by sunlight(SRC). Source: Hazardous Substances Data Bank (HSDB)
- Consumer Uses: Not Known or Reasonably Ascertainable; Solvent; Fuel agents Source: EPA Chemical Data Reporting (CDR)
- Industry Uses: Solvent; Absorbent; Humectant; Fuel agents; Processing aids not otherwise specified; Adhesion/cohesion promoter; Intermediate Source: EPA Chemical Data Reporting (CDR)
- Cosmetic Ingredient Review Link: CIR ingredient: 2-Methoxyethanol Source: Cosmetic Ingredient Review (CIR)
- Sources/Uses: Used as a solvent for many different purposes, (e.g., varnishes, dyes, and resins) and as a jet deicing additive; [ACGIH] Used in the Asian microelectronics industry in photoresist formulations and in manufacturing copper-laminate circuit boards; [JOEM 2004;46:707-713] Source: Haz-Map, Information on Hazardous Chemicals and Occupational Diseases
- Industrial Processes with risk of exposure: Semiconductor Manufacturing [Category: Industry]; Painting (Solvents) [Category: Paint]; Textiles (Printing, Dyeing, or Finishing) [Category: Industry] Source: Haz-Map, Information on Hazardous Chemicals and Occupational Diseases
- Uses: For 2-methoxyethanol (USEPA/OPP Pesticide Code: 042202) there are 0 labels match. /SRP: Not registered for current use in the U.S., but approved pesticide uses may change periodically and so federal, state and local authorities must be consulted for currently approved uses./ Source: Hazardous Substances Data Bank (HSDB)
- Uses: The active ingredient is no longer contained in any registered products ... "cancelled." Source: Hazardous Substances Data Bank (HSDB)
- Uses: Solvent for nitrocellulose, ... solvent mixtures, lacquers, ... perfume fixative, ... jet fuel deicing additive. Source: Hazardous Substances Data Bank (HSDB)
- Uses: Solvent for low viscosity cellulose acetate, natural resins, some synthetic resins and some alc-sol dyes; in dyeing leather; sealing moisture-proof cellophane; in nail polishes, quick drying varnishes and enamels, wood stains. In modified Karl Fischer reagent. Source: Hazardous Substances Data Bank (HSDB)
- Uses: For more Uses (Complete) data for 2-METHOXYETHANOL (8 total), please visit the HSDB record page. Source: Hazardous Substances Data Bank (HSDB)
- Uses: Methyl cellosolve, is a clear and colorless liquid at room temperature mainly used as a solvent. It is used for many purposes including varnishes, dyes, resins, printing, finishing textile, and semiconductor manufacturing. Source: Toxin and Toxin Target Database (T3DB)
Mapped by: Existing checksum-valid CAS to unique PubChem CID match. Retrieved: 2026-08-31. Open source record
Scientific classifications and hazard annotations provide context and do not replace the market-specific regulatory decision shown above.
Additional source coverage and match status
| Source | Result | Checked |
|---|---|---|
| NIH PubChem PUG-View | Exact match | 2026-08-31 |
A recorded no-match is useful evidence that the source was checked; it is not a claim that the substance does not exist elsewhere.
Retrieved from NIH PubChem on 2026-08-31 by checksum-valid CAS matching. Chemical properties do not replace the regulatory decision on this page.
Verified chemistry for CAS 110-49-6
Ethylene glycol monomethyl ether acetate
Ethylene Glycol Monomethyl Ether Acetate can cause developmental toxicity and male reproductive toxicity according to The National Institute for Occupational Safety and Health (NIOSH). — California Office of Environmental Health Hazard Assessment (OEHHA)
- IUPAC name
- 2-methoxyethyl acetate
- Molecular formula
- C5H10O3
- Molecular weight
- 118.13 g/mol
- Exact mass
- 118.062994177 Da
- Monoisotopic mass
- 118.062994177 Da
- XLogP3
- 0.0
- Topological polar surface area
- 35.5 Ų
- Molecular complexity
- 70.0
- Formal charge
- 0
- Hydrogen-bond donors
- 0
- Hydrogen-bond acceptors
- 3
- Rotatable bonds
- 4
- Heavy atoms
- 8
- Covalent units
- 1
Names and synonyms reported to PubChem
16 more reported names
External database identifiers
Advanced structure statistics
- Defined atom stereocentres
- 0
- Undefined atom stereocentres
- 0
- Defined bond stereocentres
- 0
- Undefined bond stereocentres
- 0
- 3D pharmacophore features
- 2
- 3D rings
- 0
- 3D hydrophobes
- 0
- 3D acceptor features
- 2
- 3D donor features
- 0
- 3D anionic centres
- 0
- 3D cationic centres
- 0
- 3D conformers
- 10
- Effective 3D rotors
- 4.0
Machine-readable structure identifiers
- SMILES
CC(=O)OCCOC- InChI
InChI=1S/C5H10O3/c1-5(6)8-4-3-7-2/h3-4H2,1-2H3- InChIKey
XLLIQLLCWZCATF-UHFFFAOYSA-N
Evidence from additional scientific databases
NIH PubChem PUG-View
Attributed physical-property, hazard, environmental and use annotations.
- Autoignition Temperature: 740 °F (USCG, 1999) Source: CAMEO Chemicals
- Autoignition Temperature: 394 °C, 740 °F Source: Hazardous Substances Data Bank (HSDB)
- Autoignition Temperature: 380 °C Source: ILO-WHO International Chemical Safety Cards (ICSCs)
- Boiling Point: 293 °F at 760 mmHg (NTP, 1992) Source: CAMEO Chemicals
- Boiling Point: 145 °C Source: Hazardous Substances Data Bank (HSDB)
- Boiling Point: 145 °C Source: ILO-WHO International Chemical Safety Cards (ICSCs)
- Boiling Point: 293 °F Source: Occupational Safety and Health Administration (OSHA)
- Boiling Point: 143 °C @760 [mm Hg] Source: PAC Chemical Database, U.S. Department of Energy
- Boiling Point: 293 °F Source: The National Institute for Occupational Safety and Health (NIOSH)
- Color/Form: Colorless liquid Source: Hazardous Substances Data Bank (HSDB)
- Density: 1.006 at 68 °F (USCG, 1999) - Denser than water; will sink Source: CAMEO Chemicals
- Density: 1.0074 g/cu cm at 19 °C Source: Hazardous Substances Data Bank (HSDB)
- Density: Bulk density: 8.4 lb/gal at 20 °C Source: Hazardous Substances Data Bank (HSDB)
- Density: Relative density (water = 1): 1.01 Source: ILO-WHO International Chemical Safety Cards (ICSCs)
- Density: 1.006 Source: Occupational Safety and Health Administration (OSHA)
- Density: 1.005 @ 20°C Source: PAC Chemical Database, U.S. Department of Energy
- Density: 1.01 Source: The National Institute for Occupational Safety and Health (NIOSH)
- Flash Point: 111 °F (NTP, 1992) Source: CAMEO Chemicals
- Flash Point: 111 °F Source: Haz-Map, Information on Hazardous Chemicals and Occupational Diseases
- Flash Point: 45 °C (120 °F) (CLOSED CUP) Source: Hazardous Substances Data Bank (HSDB)
- Flash Point: 55.6 °C (Open cup) Source: Hazardous Substances Data Bank (HSDB)
- Flash Point: 45 °C c.c. Source: ILO-WHO International Chemical Safety Cards (ICSCs)
- Flash Point: 120 °F Source: Occupational Safety and Health Administration (OSHA)
- Flash Point: 120 °F Source: The National Institute for Occupational Safety and Health (NIOSH)
- LogP: 0.121 Source: ILO-WHO International Chemical Safety Cards (ICSCs)
- Melting Point: -85 °F (NTP, 1992) Source: CAMEO Chemicals
- Melting Point: -65.1 °C Source: Hazardous Substances Data Bank (HSDB)
- Melting Point: -65 °C Source: ILO-WHO International Chemical Safety Cards (ICSCs)
- Melting Point: -85 °F Source: Occupational Safety and Health Administration (OSHA)
- Melting Point: -70 °C Source: PAC Chemical Database, U.S. Department of Energy
- Melting Point: -85 °F Source: The National Institute for Occupational Safety and Health (NIOSH)
- Odor: Pleasant odor Source: Hazardous Substances Data Bank (HSDB)
- Odor: Ester-like odor Source: Hazardous Substances Data Bank (HSDB)
- Physical Description: Ethylene glycol monomethyl ether acetate appears as a clear colorless liquid with a pleasant odor. Flash point of 135 °F. Denser than water and soluble in water. Vapors are heavier than air. Source: CAMEO Chemicals
- Physical Description: Colorless liquid with a pleasant odor; [CAMEO] Source: Haz-Map, Information on Hazardous Chemicals and Occupational Diseases
- Physical Description: COLOURLESS LIQUID WITH CHARACTERISTIC ODOUR. Source: ILO-WHO International Chemical Safety Cards (ICSCs)
- Physical Description: Colorless liquid with a mild, ether-like odor. Source: Occupational Safety and Health Administration (OSHA)
- Physical Description: Colorless liquid with a mild, ether-like odor. Source: The National Institute for Occupational Safety and Health (NIOSH)
- Refractive Index: Index of refraction: 1.4019 at 20 °C/D Source: Hazardous Substances Data Bank (HSDB)
- Solubility: greater than or equal to 100 mg/mL at 68 °F (NTP, 1992) Source: CAMEO Chemicals
- Solubility: Hildebrand solubility parameter(delta) = 18.8 MPa; Coefficient of expansion = 0.00110 °C-1 at 20 °C Source: Hazardous Substances Data Bank (HSDB)
- Solubility: Miscible with most organic solvents, oils Source: Hazardous Substances Data Bank (HSDB)
- Solubility: Very soluble in water, ethyl ether, and ethanol; soluble in carbon tetrachloride. Source: Hazardous Substances Data Bank (HSDB)
- Solubility: Infinitely soluble in water at 25 °C; water infinitely soluble in methyl cellosolve acetate at 25 °C Source: Hazardous Substances Data Bank (HSDB)
- Solubility: Solubility in water: miscible Source: ILO-WHO International Chemical Safety Cards (ICSCs)
- Solubility: Miscible Source: The National Institute for Occupational Safety and Health (NIOSH)
- Vapor Pressure: 2 mmHg at 68 °F (NTP, 1992) Source: CAMEO Chemicals
- Vapor Pressure: 7.0 [mmHg] Source: Haz-Map, Information on Hazardous Chemicals and Occupational Diseases
- Vapor Pressure: Vapor pressure = 2 torr at 20 °C Source: Hazardous Substances Data Bank (HSDB)
- Vapor Pressure: 7.0 mm Hg at 20 °C Source: Hazardous Substances Data Bank (HSDB)
- Vapor Pressure: Vapor pressure, kPa at 20 °C: 0.27 Source: ILO-WHO International Chemical Safety Cards (ICSCs)
- Vapor Pressure: 5 mmHg Source: Occupational Safety and Health Administration (OSHA)
- Vapor Pressure: 2 [mm Hg] @20 °C Source: PAC Chemical Database, U.S. Department of Energy
- Vapor Pressure: 2 mmHg Source: The National Institute for Occupational Safety and Health (NIOSH)
- Viscosity: 1.1 cP at 25 °C Source: Hazardous Substances Data Bank (HSDB)
- Exposure Routes: The substance can be absorbed into the body by inhalation of its vapour, through the skin and by ingestion. Source: ILO-WHO International Chemical Safety Cards (ICSCs)
- Exposure Routes: inhalation, skin absorption, ingestion, skin and/or eye contact Source: The National Institute for Occupational Safety and Health (NIOSH)
- First Aid: EYES: First check the victim for contact lenses and remove if present. Flush victim's eyes with water or normal saline solution for 20 to 30 minutes while simultaneously calling a hospital or poison control center. Do not put any ointments, oils, or medication in the victim's eyes without specific instructions from a physician. IMMEDIATELY transport the victim after flushing eyes to a hospital even if no symptoms (such as redness or irritation) develop.; SKIN: IMMEDIATELY flood affected skin with water while removing and isolating all contaminated clothing. Gently wash all affected skin areas thoroughly with soap and water. If symptoms such as redness or irritation develop, IMMEDIATELY call a physician and be prepared to transport the victim to a hospital for treatment.; INHALATION: IMMEDIATELY leave the contaminated area; take deep breaths of fresh air. If symptoms (such as wheezing, coughing, shortness of breath, or burning in the mouth, throat, or chest) develop, call a physician and be prepared to transport the victim to a hospital. Provide proper respiratory protection to rescuers entering an unknown atmosphere. Whenever possible, Self-Contained Breathing Apparatus (SCBA) shou Source: CAMEO Chemicals
- ERG2024, Guide 129 (Ethylene glycol monomethyl ether acetate): General First Aid:; · Call 911 or emergency medical service.; · Ensure that medical personnel are aware of the material(s) involved, take precautions to protect themselves and avoid contamination.; · Move victim to fresh air if it can be done safely.; · Administer oxygen if breathing is difficult.; · If victim is not breathing:; -- DO NOT perform mouth-to-mouth resuscitation; the victim may have ingested or inhaled the substance.; -- If equipped and pulse detected, wash face and mouth, then give artificial respiration using a proper respiratory medical device (bag-valve mask, pocket mask equipped with a one-way valve or other device).; -- If no pulse detected or no respiratory medical device available, provide continuous compressions. Conduct a pulse check every two minutes or monitor for any signs of spontaneous respirations.; · Remove and isolate contaminated clothing and shoes.; · For minor skin contact, avoid spreading material on unaffected skin.; · In case of contact with substance, remove immediately by flushing skin or eyes with running water for at least 20 minutes.; · For severe burns, immediate medical attention is required.; · Effects of exposure (inhalation, ingestion, Source: Emergency Response Guidebook (ERG)
- First Aid: (General first aid procedures); Eye: Irrigate immediately - If this chemical contacts the eyes, immediately wash (irrigate) the eyes with large amounts of water, occasionally lifting the lower and upper lids. Get medical attention immediately.; Skin: Water flush promptly - If this chemical contacts the skin, flush the contaminated skin with water promptly. If this chemical penetrates the clothing, immediately remove the clothing and flush the skin with water promptly. If irritation persists after washing, get medical attention.; Breathing: Respiratory support; Swallow: Medical attention immediately - If this chemical has been swallowed, get medical attention immediately. Source: The National Institute for Occupational Safety and Health (NIOSH)
- Signal: Danger Source: Regulation (EC) No 1272/2008 of the European Parliament and of the Council
- GHS Hazard Statements: H302: Harmful if swallowed [Warning Acute toxicity, oral]; H312: Harmful in contact with skin [Warning Acute toxicity, dermal]; H332: Harmful if inhaled [Warning Acute toxicity, inhalation]; H360FD: May damage fertility; May damage the unborn child [Danger Reproductive toxicity] Source: Regulation (EC) No 1272/2008 of the European Parliament and of the Council
- Precautionary Statement Codes: P203, P261, P264, P270, P271, P280, P301+P317, P302+P352, P304+P340, P317, P318, P321, P330, P362+P364, P405, and P501 (click each P-code to see the statement) Source: Regulation (EC) No 1272/2008 of the European Parliament and of the Council
- Signal: Danger Source: European Chemicals Agency (ECHA)
- GHS Hazard Statements: H226 (39.6%): Flammable liquid and vapor [Warning Flammable liquids]; H302+H312+H332 (38.6%): Harmful if swallowed, in contact with skin or if inhaled [Warning Acute toxicity, oral; acute toxicity, dermal; acute toxicity, inhalation]; H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]; H312 (100%): Harmful in contact with skin [Warning Acute toxicity, dermal]; H332 (100%): Harmful if inhaled [Warning Acute toxicity, inhalation]; H360 (99%): May damage fertility or the unborn child [Danger Reproductive toxicity] Source: European Chemicals Agency (ECHA)
- Precautionary Statement Codes: P203, P210, P233, P240, P241, P242, P243, P261, P264, P270, P271, P280, P301+P317, P302+P352, P303+P361+P353, P304+P340, P317, P318, P321, P330, P362+P364, P370+P378, P403+P235, P405, and P501 (click each P-code to see the statement) Source: European Chemicals Agency (ECHA)
- ECHA C&L Notifications Summary: Aggregated GHS information provided per 101 reports by companies from 8 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.; Information may vary between notifications depending on impurities, additives, and other factors. The percentage value in parenthesis indicates the notified classification ratio from companies that provide hazard codes. Only hazard codes with percentage values above 10% are shown. For more detailed information, please visit ECHA C&L website. Source: European Chemicals Agency (ECHA)
- Signal: Danger Source: NITE-CMC
- GHS Hazard Statements: H226: Flammable liquid and vapor [Warning Flammable liquids]; H320: Causes eye irritation [Warning Serious eye damage/eye irritation]; H336: May cause drowsiness or dizziness [Warning Specific target organ toxicity, single exposure; Narcotic effects]; H360: May damage fertility or the unborn child [Danger Reproductive toxicity]; H370: Causes damage to organs [Danger Specific target organ toxicity, single exposure]; H372: Causes damage to organs through prolonged or repeated exposure [Danger Specific target organ toxicity, repeated exposure] Source: NITE-CMC
- Precautionary Statement Codes: P203, P210, P233, P240, P241, P242, P243, P260, P261, P264, P264+P265, P270, P271, P280, P303+P361+P353, P304+P340, P305+P351+P338, P308+P316, P318, P319, P321, P337+P317, P370+P378, P403+P233, P403+P235, P405, and P501 (click each P-code to see the statement) Source: NITE-CMC
- GHS Hazard Statements: H226: Flammable liquid and vapor [Warning Flammable liquids]; H320: Causes eye irritation [Warning Serious eye damage/eye irritation]; H331: Toxic if inhaled [Danger Acute toxicity, inhalation]; H360: May damage fertility or the unborn child [Danger Reproductive toxicity]; H370: Causes damage to organs [Danger Specific target organ toxicity, single exposure]; H373: May causes damage to organs through prolonged or repeated exposure [Warning Specific target organ toxicity, repeated exposure]; H402: Harmful to aquatic life [Hazardous to the aquatic environment, acute hazard]; H411: Toxic to aquatic life with long lasting effects [Hazardous to the aquatic environment, long-term hazard] Source: NITE-CMC
- Precautionary Statement Codes: P203, P210, P233, P240, P241, P242, P243, P260, P261, P264, P264+P265, P270, P271, P273, P280, P303+P361+P353, P304+P340, P305+P351+P338, P308+P316, P316, P318, P319, P321, P337+P317, P370+P378, P391, P403+P233, P403+P235, P405, and P501 (click each P-code to see the statement) Source: NITE-CMC
- NFPA Health Rating: 0 - Materials that, under emergency conditions, would offer no hazard beyond that of ordinary combustible materials. Source: Hazardous Substances Data Bank (HSDB)
- NFPA Fire Rating: 2 - Materials that must be moderately heated or exposed to relatively high ambient temperatures before ignition can occur. Materials would not under normal conditions form hazardous atmospheres with air, but under high ambient temperatures or under moderate heating could release vapor in sufficient quantities to produce hazardous atmospheres with air. Source: Hazardous Substances Data Bank (HSDB)
- NFPA Instability Rating: 0 - Materials that in themselves are normally stable, even under fire conditions. Source: Hazardous Substances Data Bank (HSDB)
- Target Organs: Eyes, respiratory system, kidneys, brain, central nervous system, peripheral nervous system, reproductive system, hematopoietic system Source: The National Institute for Occupational Safety and Health (NIOSH)
- Toxicity Summary: ... The methyl and ethyl ethers of ethylene glycol, ie 2- methoxyethanol (2-ME) esters, 2-methoxyethyl acetate (2-MEA) and 2-ethoxyethyl acetate (2- EEA) ... are all stable, and are all miscible with (or in the case of 2-EEA very soluble in) water and miscible with a large number of organic solvents. ... The solubility of these glycol ethers in water and their relatively low vapor pressure could result in their build-up in water in the absence of degradation. However, degradation by microorganisms in soil, sewage sludge, and water appears to prevent this possibility. Atmospheric emissions resulting from the use of glycol ethers as evaporative solvents result in the greatest environmental exposure.... Effects on Organisms in the Environment: The toxicity of 2-ME and 2-EE to microorganisms and aquatic animals appears to be low. ... The glycol ether acetates (2-MEA and 2-EEA) are far more toxic to fish. The LC50 of 2-EEA for fathead minnows is 46 mg/L and that of 2-MEA for tidewater silverfish and bluegills is 45 mg/L. ... Effects on Experimental Animals and In Vitro Test Systems: Systemic toxicity: The toxicity of 2-ME and 2-EE to experimental animals has been much more widely studie Source: Hazardous Substances Data Bank (HSDB)
- Environmental Bioconcentration: An estimated BCF of 3.2 was calculated for methyl cellosolve acetate(SRC), using an estimated log Kow of 0.10(1) and a regression-derived equation(2). According to a classification scheme(3), this BCF suggests that bioconcentration in aquatic organisms is low(SRC). Source: Hazardous Substances Data Bank (HSDB)
- Environmental Fate: TERRESTRIAL FATE: Based on a classification scheme(1), an estimated Koc value of 30(SRC), determined from an estimated log Kow of 0.10(2) and a regression-derived equation(3), indicates that methyl cellosolve acetate is expected to have very high mobility in soil(SRC). Volatilization of methyl cellosolve acetate from moist soil surfaces is expected to be an important fate process(SRC) given an estimated Henry's Law constant of 1.1X10-6 atm-cu m/mole(SRC) derived from its vapor pressure, 7.0 mm Hg at 20 °C(4), and assigned value for water solubility of 1.0X10+6 mg/L (miscible)(5). The potential for volatilization of methyl cellosolve acetate from dry soil surfaces may exist(SRC) based on its vapor pressure(4). Using aqueous screening tests methyl cellosolve acetate reached 30 to 86.9% of its theoretical BOD over a period of 5 to 14 days(6,7), suggesting that biodegradation may be an important environmental fate process in soil(SRC). Source: Hazardous Substances Data Bank (HSDB)
- Environmental Fate: AQUATIC FATE: Based on a classification scheme(1), an estimated Koc value of 30(SRC), determined from an estimated log Kow of 0.10(2) and a regression-derived equation(3), indicates that methyl cellosolve acetate is not expected to adsorb to suspended solids and sediment(SRC). Volatilization from water surfaces is expected(3) based upon an estimated Henry's Law constant of 1.1X10-6 atm-cu m/mole(SRC) derived from its vapor pressure, 7.0 mm Hg(4), and assigned value for water solubility of 1.0X10+6 mg/L (miscible)(5). Using this Henry's Law constant and an estimation method(3), volatilization half-lives for a model river and model lake are 24 days and 270 days, respectively(SRC). According to a classification scheme(6), an estimated BCF of 3.2(3), from an estimated log Kow(2), and a regression derived equation(7) suggests that bioconcentration in aquatic organisms is low(SRC). Hydrolysis half-lives of 140 and 14 days at pH values of 7 and 8, respectively(10), suggest that hydrolysis is not expected to be an important process except under basic conditions(SRC). Using aqueous screening tests, methyl cellosolve acetate reached 30 to 86.9% of its theoretical BOD over a period of 5 to 14 Source: Hazardous Substances Data Bank (HSDB)
- Environmental Fate: ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), methyl cellosolve acetate, which has a measured vapor pressure of 7.0 mm Hg at 20 °C(2), is expected to exist solely as a vapor in the ambient atmosphere. Vapor-phase methyl cellosolve acetate is degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals(SRC); the half-life for this reaction in air is estimated to be about 1.1 days(SRC) calculated from its rate constant of 9.7X10-12 cu cm/molecule-sec at 25 °C(SRC)that was derived using a structure estimation method(3). Methyl cellosolve acetate does not contain chromophores that absorb at wavelengths >290 nm(4) and therefore is not expected to be susceptible to direct photolysis by sunlight(SRC). Source: Hazardous Substances Data Bank (HSDB)
- Sources/Uses: Used as a solvent and in the production of photographic films and textile printing; [ACGIH] Source: Haz-Map, Information on Hazardous Chemicals and Occupational Diseases
- Restricted Notes: The Semiconductor Industry Association recommends elimination of this solvent because of potential reproductive effects. [CHS, p. 43] Source: Haz-Map, Information on Hazardous Chemicals and Occupational Diseases
- Industrial Processes with risk of exposure: Semiconductor Manufacturing [Category: Industry]; Textiles (Printing, Dyeing, or Finishing) [Category: Industry] Source: Haz-Map, Information on Hazardous Chemicals and Occupational Diseases
- Uses: Solvent for nitrocellulose, cellulose acetate, various gums, resins, waxes, oils; textile printing; photographic film; lacquers; dopes Source: Hazardous Substances Data Bank (HSDB)
- Uses: Used in silkscreening inks Source: Hazardous Substances Data Bank (HSDB)
- Uses: Industrial solvent Source: Hazardous Substances Data Bank (HSDB)
Mapped by: Existing checksum-valid CAS to unique PubChem CID match. Retrieved: 2026-08-31. Open source record
Scientific classifications and hazard annotations provide context and do not replace the market-specific regulatory decision shown above.
Additional source coverage and match status
| Source | Result | Checked |
|---|---|---|
| NIH PubChem PUG-View | Exact match | 2026-08-31 |
A recorded no-match is useful evidence that the source was checked; it is not a claim that the substance does not exist elsewhere.
Retrieved from NIH PubChem on 2026-08-31 by checksum-valid CAS matching. Chemical properties do not replace the regulatory decision on this page.
Official source and provenance
- Registered source
- Great Britain Cosmetics Regulation — consolidated Annexes II–VI and amendments
- Source reference
- GB Cosmetics Regulation, Annex II, entry 665
- Source record ID
II-665- Source version
- 2026-08-15
- Source language
- English
- Translation status
- Original is English
- Effective date
- 2026-08-15
- Source updated
- 2026-08-19
- Snapshot checked
- 2026-08-30 04:51 UTC
- Validation method
- legislation.gov.uk XML table parse; {'II': 1758, 'III': 326, 'IV': 154, 'V': 57, 'VI': 34}
- SHA-256
e3a386d950f54c6e7a7f9e784d1bd46e52de725137e89d5630709824475215d8
Registered dataset notes
- Dataset coverage
- Complete consolidated GB Annexes II–VI, with later amendments versioned separately
- Authority note
- Binding GB schedules and versioned amendments to retained Regulation 1223/2009; applies to England, Wales and Scotland, not Northern Ireland
- Source licence
- Open Government Licence v3.0 / Crown copyright
- Attribution
- Contains public sector information licensed under the Open Government Licence v3.0.
How this record fits the market dataset
Status distribution
Condition text is present on 517 of 2329 current records. An empty condition field is interpreted according to the record type above; it is never converted into an unrestricted-use claim.
Great Britain market context
Complete consolidated annex dataset
Coverage version: GB retained Regulation 1223/2009 schedules, effective 15 August 2026
Current consolidated Annexes II–VI for England, Scotland and Wales.
Verification checklist
- Confirm INCI/CAS/EC identity.
- Review every current GB Annex II–VI match.
- Check commencement dates and later statutory instruments.
- Verify SCPN, responsible-person, safety-report and labelling duties.
Official market sources
- Great Britain Cosmetics Regulation — consolidated Annexes II–VI and amendmentsBinding GB schedules and versioned amendments to retained Regulation 1223/2009; applies to England, Wales and Scotland, not Northern Ireland
Verification workflow and record completeness
Before using this result in a compliance decision
- Confirm that “2-Methoxyethanol and its acetate (2-Methoxyethyl acetate)” and every CAS/EC identifier refer to the material in your supplier specification.
- Confirm INCI/CAS/EC identity.
- Review every current GB Annex II–VI match.
- Check commencement dates and later statutory instruments.
- Verify SCPN, responsible-person, safety-report and labelling duties.
- Document the source version and recheck the regulator before manufacture, notification or market placement.
Fields available in this record
- Official substance nameAvailable
- CASAvailable
- ECAvailable
- Separate condition textNot present in source row
- Effective dateAvailable
- Snapshot hash and methodAvailable
Questions this page answers
Stable citation
2-Methoxyethanol and its acetate (2-Methoxyethyl acetate). GB Cosmetics Regulation, Annex II, entry 665. Great Britain. Source version 2026-08-15. CosIng Checker regulatory record: https://cosingchecker.com/regulations/gb/records/5020/
Cite the regulator as the legal authority. This page is a structured evidence index and verification aid, not a substitute for the official text or professional legal assessment.
Interpretation and limits for Great Britain
This official record identifies the substance as prohibited for cosmetic use in the stated market scope.
Do not rely on a formulation containing this identity until the cited source, effective date and exact substance match have been verified.
How to interpret the legal role
The cited row forms part of a binding rule or legally incorporated list for this market.
Evidence on this page
- Recorded outcome: Prohibited
- Legal role: Binding rule
- Source version: 2026-08-15
- Effective date: 2026-08-15
What it does not prove
No annex match is not approval and does not cover Northern Ireland, which follows the applicable EU framework.
Further authoritative substance research
These sources can add identity, safety, exposure or hazard context. A link is not evidence that the database contains this exact substance, and none of these sources overrides the market decision above.
Cosmetic Ingredient Review safety assessments
Expert Panel conclusions, assessed ingredient groups, use conditions, dates and report documents
Independent expert review considered by FDA; not a government approval or binding market rule
Research this identity at the sourceFDA Global Substance Registration System
UNII identifiers, preferred names, substance types, codes and public substance relationships
Identity registry only; UNII availability does not imply FDA review or approval
Research this identity at the sourceILO/WHO International Chemical Safety Cards
Hazards, symptoms, first aid, storage, incompatibilities and physical properties for covered chemicals
International occupational chemical-safety reference; not cosmetic-use approval
Research this identity at the sourceJapan NITE-CHRIP
Chemical identity, Japanese and foreign legal lists, GHS hazards and exposure-related information
Chemical-management evidence; cosmetic status remains governed by the applicable MHLW standard and market rules
Research this identity at the sourceNIOSH Pocket Guide to Chemical Hazards
REL, PEL, IDLH, properties, exposure routes, symptoms, target organs, first aid and measurement methods for covered workplace chemicals
US occupational-health guidance and limits; not a cosmetic ingredient decision
Research this identity at the sourceOECD eChemPortal
Gateway to authority-owned physical-property, fate, ecotoxicity, toxicity, exposure and GHS records
Discovery gateway; each linked authority remains responsible for its data
Research this identity at the sourceUS EPA CompTox CTX APIs
API key required for importDTXSID identity, experimental and predicted properties, toxicity, bioactivity, exposure and environmental data
Scientific and computational evidence; predictions must remain labelled and do not determine cosmetic legality
Research this identity at the source