(R)-(-)-2-pentanol

2-pentanol, (2R)-

CAS: 31087-44-2 C5 H12 O MW: 88.14984000

Identification

Name(R)-(-)-2-pentanol
CAS Number31087-44-2
FDA UNIISearch
Molecular FormulaC5 H12 O
Molecular Weight88.14984000
MDL NumberMFCD00065953
Nikkaji NumberJ75.835C
Beilstein4652311
XlogP31.20 (est)

Regulatory

Physical Properties

Appearance colorless clear liquid (est)
Assay 97.00 to 100.00
Food Chemicals Codex Listed No
Specific Gravity 0.80600 to 0.81100 @ 20.00 °C.
Pounds per Gallon - (est). 6.715 to 6.756
Refractive Index 1.40500 to 1.40700 @ 20.00 °C.
Optical Rotation -15.0 to -12.0
Boiling Point 118.00 to 119.00 °C. @ 760.00 mm Hg (est)
Vapor Pressure 8.047000 mmHg @ 25.00 °C. (est)
Vapor Density 3.0 ( Air = 1 )
Flash Point 93.00 °F. TCC ( 34.00 °C. )
logP (o/w) 1.223 (est)
Soluble in alcohol
Insoluble in water

Organoleptic Properties

Odor Description light seedy sharp

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

Categoryflavoring agents
Recommendation for (R)-(-)-2-pentanol usage levels up tonot for fragrance use.

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Potential Uses

None Found

Natural Occurrence

not found in nature

Synonyms

(2R)- pentan-2-ol (R)(-)-2- pentanol 2- pentanol, (2R)- PubMed: The substrate binding cavity of particulate methane monooxygenase from Methylosinus trichosporium OB3b expresses high enantioselectivity for n-butane and n-pentane oxidation to 2-alcohol. PubMed: Separation of enantiomers in microemulsion electrokinetic chromatography using chiral alcohols as cosurfactants. PubMed: The stereoselectivity and catalytic properties of Xanthobacter autotrophicus 2-[(R)-2-Hydroxypropylthio]ethanesulfonate dehydrogenase are controlled by interactions between C-terminal arginine residues and the sulfonate of coenzyme M. PubMed: Characterization of the 2-[(R)-2-hydroxypropylthio]ethanesulfonate dehydrogenase from Xanthobacter strain Py2: product inhibition, pH dependence of kinetic parameters, site-directed mutagenesis, rapid equilibrium inhibition, and chemical modification. PubMed: Short-range interactions within molecular complexes formed in supersonic beams: structural effects and chiral discrimination PubMed: Determination of ketorolac enantiomers in plasma using enantioselective liquid chromatography on an alpha 1-acid glycoprotein chiral stationary phase and ultraviolet detection.