methyl 6-hydroxyhexanoate
hexanoic acid, 6-hydroxy-, methyl ester
Identification
| Name | methyl 6-hydroxyhexanoate |
| CAS Number | 4547-43-7 |
| FDA UNII | Search |
| Molecular Formula | C7 H14 O3 |
| Molecular Weight | 146.18618000 |
| MDL Number | MFCD00083576 |
| Nikkaji Number | J140.278A |
Regulatory
Physical Properties
| Assay | 95.00 to 100.00 |
| Food Chemicals Codex Listed | No |
| Boiling Point | 199.60 °C. @ 760.00 mm Hg (est) |
| Vapor Pressure | 0.100000 mmHg @ 25.00 °C. (est) |
| Flash Point | 165.00 °F. TCC ( 73.80 °C. ) (est) |
| logP (o/w) | 0.300 (est) |
| Soluble in | water, 4.585e+004 mg/L @ 25 °C (est) |
No sensory data available
Safety Information
| Oral/Parenteral Toxicity | Not determined |
| Dermal Toxicity | Not determined |
| Inhalation Toxicity | Not determined |
GHS Classification
['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']
Safety in Use
| Category | information only not used for fragrances or flavors |
| Recommendation for methyl 6-hydroxyhexanoate usage levels up to | not for fragrance use. |
| Recommendation for methyl 6-hydroxyhexanoate flavor usage levels up to | not for flavor use. |
BOC Sciences
Best of Chemicals Supplier
Quality supplier of research chemicals and biochemicals including inhibitors, building blocks, GMP Products, impurities and metabolites, APIs for Veterinary, Natural Compounds, ADCs, Stem Cell Molecul...
Potential Uses
Natural Occurrence
Synonyms
hexanoic acid, 6-hydroxy-, methyl ester
6-
hydroxyhexanoic acid methyl ester
6-
hydroxyhexanoicacidmethylester
methyl 6-hydroxycapronate
PubMed:
Synthesis and Molecular Structure of the 5-Methoxycarbonylpentyl α-Glycoside of the Upstream, Terminal Moiety of the O-Specific Polysaccharide of Vibrio cholerae O1, Serotype Inaba.
PubMed:
Introducing an inâ
situ capping strategy in systems biocatalysis to access 6-aminohexanoic acid.
PubMed:
Microbial/enzymatic synthesis of chiral drug intermediates.
PubMed:
Synthesis of a novel ether-bridged GM3-lactone analogue as a target for an antibody-based cancer therapy.
PubMed:
Synthesis of eight glycosides of hexasaccharide fragments representing the terminus of the O-polysaccharide of Vibrio cholerae O:1, serotype Inaba and Ogawa, bearing aglycons suitable for linking to proteins.
PubMed:
Agents for alkylating steroid hormone receptors. 3. Omega-substituted esters of 17-alpha-hydroxyprogesterone.