2-OCTANOL

Details

Stereochemistry	RACEMIC
Molecular Formula	C8H18O
Molecular Weight	130.2279
Optical Activity	( + / - )
Defined Stereocenters	0 / 1
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

SMILES

CCCCCCC(C)O

InChI

InChIKey=SJWFXCIHNDVPSH-UHFFFAOYSA-N

InChI=1S/C8H18O/c1-3-4-5-6-7-8(2)9/h8-9H,3-7H2,1-2H3

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Approval Year

PubMed

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Title	Date	PubMed
Photoswitching of ferroelectric liquid crystals using chiral thioindigo dopants: The development of a photochemical switch hitter.	2004	14762829
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.	2004 Jun 1	15157110
High-yield conversion of (R)-2-octanol from the corresponding racemate by stereoinversion using Candida rugosa.	2005 Jan	15685415
Effect of lipase immobilization on resolution of (R, S)-2-octanol in nonaqueous media using modified ultrastable-Y molecular sieve as support.	2006 Jul	16891665
Core-shell type of nanoparticles composed of poly[(n-butyl cyanoacrylate)-co-(2-octyl cyanoacrylate)] copolymers for drug delivery application: synthesis, characterization and in vitro degradation.	2006 Nov 15	16857330

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Patents

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Name

Type

Language

2-OCTANOL

Systematic Name

English

S-OCTYL ALCOHOL

Common Name

English

CAPRYL ALCOHOL

Common Name

English

2-OCTANOL [FHFI]

Common Name

English

N-OCTAN-2-OL

Common Name

English

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Classification Tree

Code System

Code

Subpart F--Flavoring Agents and Related Substances

CFR

21 CFR 172.515

FUNCTIONAL CLASSIFICATION

JECFA EVALUATION

2-OCTANOL

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Code System

Code

Type

Description

JECFA MONOGRAPH

395

PRIMARY

SMS_ID

100000166333

PRIMARY

CHEBI

37869

PRIMARY

ECHA (EC/EINECS)

204-667-0

PRIMARY

WIKIPEDIA

2-Octanol

PRIMARY

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SUBSTANCE RECORD

66B0DD5E40

2-OCTANOL