laevo-menthyl propionate

cyclohexanol, 5-methyl-2-(1-methylethyl)-, propanoate, (1R,2S,5R)-

CAS: 4951-48-8 C13 H24 O2 MW: 212.33268000 herbal

Identification

Name	laevo-menthyl propionate
IUPAC	[(1R,2S,5R)-5-methyl-2-propan-2-ylcyclohexyl] propanoate
CAS Number	4951-48-8
EINECS	225-596-1
FDA UNII	Search
Molecular Formula	C13 H24 O2
Molecular Weight	212.33268000
Nikkaji Number	J203.204J

Regulatory

Physical Properties

Appearance	colorless clear liquid (est)
Assay	98.00 to 100.00
Food Chemicals Codex Listed	No
Specific Gravity	0.92100 @ 25.00 °C.
Refractive Index	1.42600 @ 25.00 °C.
Boiling Point	222.00 °C. @ 760.00 mm Hg
Vapor Pressure	0.027000 mmHg @ 25.00 °C. (est)
Flash Point	223.00 °F. TCC ( 106.20 °C. ) (est)
logP (o/w)	4.692 (est)
Soluble in	alcohol
Insoluble in	water
Similar Items	note

Organoleptic Properties

Odor Description

at 100.00 %.

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	flavor and fragrance agents
RIFM Fragrance Material Safety Assessment	Search

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W1399 L-Menthyl Propionate

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Potential Uses

None Found

Natural Occurrence

not found in nature

Synonyms

cyclohexanol, 5-methyl-2-(1-methylethyl)-, propanoate, (1R,2S,5R)- menthol, propionate, (-)- (-)- menthyl propionate L- menthyl propionate (1R-(1alpha, 2beta,5alpha))-5- methyl-2-(1-methyl ethyl) cyclohexanol propanoate (1R,2S,5R)-5- methyl-2-(1-methyl ethyl) cyclohexanol propanoate (1theta- (1alpha,2beta, 5alpha))-5- methyl-2-(1-methyl ethyl) cyclohexanol propanoate [(1R,2S,5R)-5- methyl-2-propan-2-ylcyclohexyl] propanoate PubMed: A combination of site-directed mutagenesis and chemical modification to improve diastereopreference of Pseudomonas alcaligenes lipase. PubMed: Enhancement in skin permeation of 5-aminolevulinic acid using l-menthol and its derivatives. PubMed: Comparison of acid anhydrides with carboxylic acids in enantioselective enzymatic esterification of racemic menthol.