Cinoxate
Japan Standards for Cosmetics: Cinoxate
The provisional English translation of the MHLW Standards for Cosmetics lists this ingredient with the stated limit or use matrix.
Regulatory decision and full conditions
- Status
- Restricted
- Legal role
- Binding rule
- Regulatory summary
- The provisional English translation of the MHLW Standards for Cosmetics lists this ingredient with the stated limit or use matrix.
- Conditions and restrictions
- Published three-column use matrix (rinse-off / leave-on / mucosal; blank means prohibited, ○ means no upper limit): ○ 5.0 5.0
Substance identity
- Official source name
- Cinoxate
- CAS
- 104-28-9
- EC
- 203-191-0
- Identity mapping
- exact INCI name
- Linked ingredient
- CINOXATE
Linked CosIng identity data
Names and aliases
CosIng description: 2-Propenoic acid, 3-(4-methoxyphenyl)-, 2-ethoxyethyl ester
Recorded cosmetic function: UV ABSORBER
Function pages:UV ABSORBER
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.
New Zealand
1 linked record · 1 with specific conditions
Open supporting recordJapan
Current record1 linked record · 1 with specific conditions
Open supporting recordSouth Korea
1 linked record · 1 with specific conditions
Open supporting recordVerified chemistry for CAS 104-28-9
Cinoxate
- IUPAC name
- 2-ethoxyethyl (E)-3-(4-methoxyphenyl)prop-2-enoate
- Molecular formula
- C14H18O4
- Molecular weight
- 250.29 g/mol
- Exact mass
- 250.12050905 Da
- Monoisotopic mass
- 250.12050905 Da
- XLogP3
- 2.4
- Topological polar surface area
- 44.8 Ų
- Molecular complexity
- 255.0
- Formal charge
- 0
- Hydrogen-bond donors
- 0
- Hydrogen-bond acceptors
- 4
- Rotatable bonds
- 8
- Heavy atoms
- 18
- Covalent units
- 1
Names and synonyms reported to PubChem
16 more reported names
External database identifiers
- ChEMBL:CHEMBL2104045
- EPA DTXSID:DTXSID101167513
Advanced structure statistics
- Defined atom stereocentres
- 0
- Undefined atom stereocentres
- 0
- Defined bond stereocentres
- 1
- Undefined bond stereocentres
- 0
- 3D pharmacophore features
- 4
- 3D rings
- 1
- 3D hydrophobes
- 0
- 3D acceptor features
- 3
- 3D donor features
- 0
- 3D anionic centres
- 0
- 3D cationic centres
- 0
- 3D conformers
- 10
- Effective 3D rotors
- 8.0
Machine-readable structure identifiers
- SMILES
CCOCCOC(=O)/C=C/C1=CC=C(C=C1)OC- InChI
InChI=1S/C14H18O4/c1-3-17-10-11-18-14(15)9-6-12-4-7-13(16-2)8-5-12/h4-9H,3,10-11H2,1-2H3/b9-6+- InChIKey
CMDKPGRTAQVGFQ-RMKNXTFCSA-N
Evidence from additional scientific databases
NIH PubChem PUG-View
Attributed physical-property, hazard, environmental and use annotations.
- Boiling Point: 388 °C at 760 mm Hg /Extrapolated from 185 °C at 2 mm Hg/ Source: Hazardous Substances Data Bank (HSDB)
- Boiling Point: BP: 185 °C at 2 mm Hg Source: Hazardous Substances Data Bank (HSDB)
- Color/Form: Viscous liquid, may have slight yellow tinge Source: Hazardous Substances Data Bank (HSDB)
- Density: 1.1000 to 1.1035 at 77 °F (NTP, 1992) Source: CAMEO Chemicals
- Density: 1.102 g/cu cm at 25 °C Source: Hazardous Substances Data Bank (HSDB)
- Flash Point: greater than 212 °F (NTP, 1992) Source: CAMEO Chemicals
- Melting Point: Solidifies below -25 °C Source: Hazardous Substances Data Bank (HSDB)
- Odor: Practically odorless Source: Hazardous Substances Data Bank (HSDB)
- Physical Description: 2-ethoxyethyl-p-methoxycinnamate is a viscous clear to pale yellow liquid. Insoluble in water. (NTP, 1992) Source: CAMEO Chemicals
- Physical Description: Viscous liquid; May be slightly yellow; [Merck Index] Source: Haz-Map, Information on Hazardous Chemicals and Occupational Diseases
- Refractive Index: Index of refraction: 1.567 at 20 °C Source: Hazardous Substances Data Bank (HSDB)
- Solubility: Insoluble (NTP, 1992) Source: CAMEO Chemicals
- Solubility: Practically insoluble in water with a solubility of approximately 0.05%. Source: Hazardous Substances Data Bank (HSDB)
- Solubility: Soluble in glycerol 0.5%, propolyene glycol 5%; miscible with alcohols and vegetable oils Source: Hazardous Substances Data Bank (HSDB)
- Vapor Pressure: 0.00034 [mmHg] Source: Haz-Map, Information on Hazardous Chemicals and Occupational Diseases
- 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
- Environmental Bioconcentration: An estimated BCF of 26 was calculated for cinoxate in fish(SRC), using an estimated log Kow of 2.65(1) and a regression-derived equation(1). According to a classification scheme(2), 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 208(SRC), determined from a structure estimation method(2), indicates that cinoxate is expected to have moderate mobility in soil(SRC). Volatilization of cinoxate from moist soil surfaces is not expected to be an important fate process(SRC) given an estimated Henry's Law constant of 5.1X10-9 atm-cu m/mole(SRC), using a fragment constant estimation method(2). Cinoxate is not expected to volatilize from dry soil surfaces(SRC) based upon an estimated vapor pressure of 1.6X10-5 mm Hg(SRC), determined from a fragment constant method(2). Cinoxate absorbs UV light in the sunlight spectrum(3) and, therefore, may be susceptible to direct photolysis on soil surfaces exposed to sunlight(SRC). No relevant data were available to assess the importance of biodegradation in the environment(SRC). Source: Hazardous Substances Data Bank (HSDB)
- Environmental Fate: AQUATIC FATE: Based on a classification scheme(1), an estimated Koc value of 208(SRC), determined from a structure estimation method(2), indicates that cinoxate may have some moderate adsorption to suspended solids and sediment(SRC). Volatilization from water surfaces is not expected(3) based upon an estimated Henry's Law constant of 5.1X10-9 atm-cu m/mole(SRC), developed using a fragment constant estimation method(1). According to a classification scheme(4), an estimated BCF of 26(SRC), from an estimated log Kow of 2.65(2) and a regression-derived equation(2), suggests the potential for bioconcentration in aquatic organisms is low (SRC). A base-catalyzed second-order hydrolysis rate constant of 2.5X10-2 L/mole-sec(SRC) was estimated using a structure estimation method(2); this corresponds to half-lives of 8.9 and 0.89 years at pH values of 7 and 8, respectively(2). Cinoxate absorbs UV light in the sunlight spectrum(5) and, therefore, may be susceptible to direct photolysis on water surfaces exposed to sunlight(SRC). No relevant data were available to assess the importance of biodegradation in the environment(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), cinoxate, which has an estimated vapor pressure of 1.6X10-5 mm Hg at 25 °C(SRC), determined from a fragment constant method(2), will exist in both the vapor and particulate phases in the ambient atmosphere. Vapor-phase cinoxate 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 6.7 hours(SRC), calculated from its rate constant of 5.7X10-11 cu cm/molecule-sec at 25 °C(SRC) that was derived using a structure estimation method(2). Vapor-phase cinoxate is also degraded in the atmosphere by reaction with ozone (SRC); the half-life for this reaction in air is estimated to be about 19 hours(SRC), calculated from its rate constant of 1.6X10-17 cu cm/molecule-sec at 25 °C(SRC) that was derived using a structure estimation method(2). Particulate-phase cinoxate may be removed from the air by wet and dry deposition(SRC). Cinoxate absorbs UV light in the sunlight spectrum(3) and, therefore, may be susceptible to direct photolysis by sunlight(SRC). Source: Hazardous Substances Data Bank (HSDB)
- Sources/Uses: Used as ultraviolet screen; [Merck Index] The cinnamates are a group of chemically related substances that are used as fragrances and flavorings and less frequently as sunscreens. [Marks, p. 219] Source: Haz-Map, Information on Hazardous Chemicals and Occupational Diseases
- Uses: For cinoxate (USEPA/OPP Pesticide Code: 076604) 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: Ultraviolet screen Source: Hazardous Substances Data Bank (HSDB)
- Uses: Sunscreening Agents 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 |
|---|---|---|
| EMBL-EBI ChEBI | No exact record | 2026-08-31 |
| 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
- Japan MHLW Standards for Cosmetics
- Source reference
- Appendix 4 section 2, entry 5
- Source record ID
appendix-4-2:5- Source version
- MHLW Notification No. 331 provisional translation, retrieved 2026-08-30
- Source language
- English provisional translation; Japanese text is canonical
- Translation status
- Regulator-hosted provisional English translation · English translation
- Snapshot checked
- 2026-08-30 04:11 UTC
- Validation method
- pdftotext -layout plus strict per-table row counts
- SHA-256
117fc949a82789ca66017163f19041cf2fcf6b5902708077c8e4f56c482dc8e2
Registered dataset notes
- Dataset coverage
- Prohibited and restricted ingredient appendices with concentration and use conditions
- Authority note
- Official MHLW standard; validate later Japanese updates before presenting current status
How this record fits the market dataset
Status distribution
Condition text is present on 117 of 117 current records. An empty condition field is interpreted according to the record type above; it is never converted into an unrestricted-use claim.
Japan market context
Complete Standards appendices dataset
Coverage version: MHLW Standards for Cosmetics official English source and Japanese amendments checked for the imported snapshot
Prohibited ingredients, restricted ingredients and permitted preservative/UV/colourant appendices present in the official standard source.
Verification checklist
- Search Japanese/English identity and CAS where present.
- Apply category and maximum-amount conditions.
- Check later MHLW notices against the Japanese source.
- Verify marketing licence, notification, labelling and quasi-drug classification.
Official market sources
- Japan MHLW Standards for CosmeticsOfficial MHLW standard; validate later Japanese updates before presenting current status
Verification workflow and record completeness
Before using this result in a compliance decision
- Confirm that “Cinoxate” and every CAS/EC identifier refer to the material in your supplier specification.
- Search Japanese/English identity and CAS where present.
- Apply category and maximum-amount conditions.
- Check later MHLW notices against the Japanese source.
- Verify marketing licence, notification, labelling and quasi-drug classification.
- 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 textAvailable
- Effective dateNot supplied
- Snapshot hash and methodAvailable
Questions this page answers
Stable citation
Cinoxate. Appendix 4 section 2, entry 5. Japan. Source version MHLW Notification No. 331 provisional translation, retrieved 2026-08-30. CosIng Checker regulatory record: https://cosingchecker.com/regulations/jp/records/692/
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 Japan
This substance is not unrestricted: cosmetic use is subject to the conditions in the cited official record.
Check product type, body area, concentration, purity and warning requirements before deciding whether a formulation is compliant.
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: Restricted
- Legal role: Binding rule
- Source version: MHLW Notification No. 331 provisional translation, retrieved 2026-08-30
What it does not prove
The Japanese text and subsequent notices are canonical; no local match is not a product-compliance conclusion.
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