1,2-heptane diol

1,2-dihydroxyheptane

CAS: 3710-31-4 C7 H16 O2 MW: 132.20292000

Identification

Name1,2-heptane diol
IUPACheptane-1,2-diol
CAS Number3710-31-4
FDA UNIISearch
Molecular FormulaC7 H16 O2
Molecular Weight132.20292000
MDL NumberMFCD01861287
Nikkaji NumberJ100.449B

Regulatory

Physical Properties

Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Boiling Point 226.00 to 227.00 °C. @ 760.00 mm Hg (est)
Vapor Pressure 0.016000 mmHg @ 25.00 °C. (est)
Flash Point 215.00 °F. TCC ( 101.70 °C. ) (est)
logP (o/w) 1.030 (est)
Soluble in alcohol
Insoluble in water

No sensory data available

Safety Information

Preferred SDSView
Oral/Parenteral ToxicityNot determined
Dermal ToxicityNot determined
Inhalation ToxicityNot determined

GHS Classification

['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']

Safety in Use

Categorynatural substances and extractives
Recommendation for 1,2-heptane diol usage levels up tonot for fragrance use.
Recommendation for 1,2-heptane diol flavor usage levels up tonot for flavor use.

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Potential Uses

None Found

Natural Occurrence

found in nature

Synonyms

1,2- dihydroxyheptane heptane-1,2-diol 1,2- heptanediol PubMed: Effect of hydrocarbon chain length in 1,2-alkanediols on percutaneous absorption of metronidazole: toward development of a general vehicle for controlled release. PubMed: Topical skin targeting effect of penetration modifiers on hairless mouse skin, pig abdominal skin and pig ear skin. PubMed: cis-Cyclo-heptane-1,2-diol. PubMed: Purification, characterization, and gene cloning of glycerol dehydrogenase from Hansenula ofunaensis, and its expression for production of optically active diol. PubMed: Heat capacity studies of formation of micelle-like structure in aqueous solutions of some alkane polyols. PubMed: Novel 1,N(6)-etheno-2'-deoxyadenosine adducts from lipid peroxidation products. PubMed: Formation of 1,N6-etheno-2'-deoxyadenosine adducts by trans,trans-2, 4-Decadienal. PubMed: Absorption, distribution, elimination and metabolism of 14C-heptaminol hydrochloride in rat.