Ethyl 4-(dimethylamino)benzoate
Parbenate is a benzoate ester that is ethyl benzoate substituted by a dimethylamino group at position 4. It is an ethyl ester, a benzoate ester and a tertiary amino compound. — ChEBI
- IUPAC name
- ethyl 4-(dimethylamino)benzoate
- Molecular formula
- C11H15NO2
- Molecular weight
- 193.24 g/mol
- Exact mass
- 193.110278721 Da
- XLogP3
- 2.9
- Topological polar surface area
- 29.5 Ų
- Hydrogen-bond donors
- 0
- Hydrogen-bond acceptors
- 3
- Covalent units
- 1
- Defined stereocentres
- 0
Also known as
16 more reported names
External database identifiers
- ChEBI:CHEBI:52073
- ChEMBL:CHEMBL3185245
- EPA DTXSID:DTXSID2044763
- PubMed:23083514
- PubMed:22940188
- PubMed:22509124
- PubMed:22349946
- PubMed:22229003
- PubMed:22199932
- PubMed:22094322
- PubMed:22032933
- PubMed:21847975
- PubMed:21726293
- PubMed:21670999
- PubMed:21579781
Evidence from additional scientific databases
EMBL-EBI ChEBI
parbenate
A benzoate ester that is ethyl benzoate substituted by a dimethylamino group at position 4.
- Formula
- C11H15NO2
- Average mass
- 193.246 g/mol
- Monoisotopic mass
- 193.11028 Da
- Formal charge
- 0
- benzoate ester — is a (CHEBI:36054)
- tertiary amino compound — is a (CHEBI:50996)
- ethyl ester — is a (CHEBI:23990)
- benzoate ester — is a (CHEBI:36054)
- tertiary amino compound — is a (CHEBI:50996)
- ethyl ester — is a (CHEBI:23990)
- 2637499 Source: PubMed
Additional curated names
Cross-references from this source
- CAS: 10287-53-3 — NIST Chemistry WebBook
- CAS: 10287-53-3 — ChemIDplus
- REGISTRY_NUMBER: 2210233 — Reaxys
- MANUAL_X_REF: CN101007773 — Patent
- MANUAL_X_REF: CN101863782 — Patent
Mapped by: Exact CAS cross-reference in the ChEBI compound record. Source updated: 2015-03-02. Retrieved: 2026-08-31. Open source record
NIH PubChem PUG-View
Attributed physical-property, hazard, environmental and use annotations.
- Physical Description: Dry Powder; Other Solid; Large Crystals Source: EPA Chemical Data Reporting (CDR)
- Physical Description: White crystalline powder; [Acros Organics MSDS] Source: Haz-Map, Information on Hazardous Chemicals and Occupational Diseases
- Note: This chemical does not meet GHS hazard criteria for 55.6% (144 of 259) of all reports. Source: European Chemicals Agency (ECHA)
- Signal: Danger Source: European Chemicals Agency (ECHA)
- GHS Hazard Statements: H360 (18.5%): May damage fertility or the unborn child [Danger Reproductive toxicity]; H360F (23.9%): May damage fertility [Danger Reproductive toxicity]; H411 (44%): Toxic to aquatic life with long lasting effects [Hazardous to the aquatic environment, long-term hazard] Source: European Chemicals Agency (ECHA)
- Precautionary Statement Codes: P203, P273, P280, P318, P391, 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 259 reports by companies from 9 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.; Reported as not meeting GHS hazard criteria per 144 of 259 reports by companies.; There are 8 notifications provided by 115 of 259 reports by companies with hazard statement code(s).; 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)
- Consumer Uses: Not Known or Reasonably Ascertainable; Photosensitive agent Source: EPA Chemical Data Reporting (CDR)
- Industry Uses: Not Known or Reasonably Ascertainable; Photosensitive agent; Tanning agents not otherwise specified Source: EPA Chemical Data Reporting (CDR)
- Sources/Uses: Used as a polymerization accelerator; [ChemIDplus] Source: Haz-Map, Information on Hazardous Chemicals and Occupational Diseases
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 | Exact match | 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.