SOLKETAL

Details

Stereochemistry	RACEMIC
Molecular Formula	C6H12O3
Molecular Weight	132.1577
Optical Activity	( + / - )
Defined Stereocenters	0 / 1
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

SMILES

CC1(C)OCC(CO)O1

InChI

InChIKey=RNVYQYLELCKWAN-UHFFFAOYSA-N

InChI=1S/C6H12O3/c1-6(2)8-4-5(3-7)9-6/h5,7H,3-4H2,1-2H3

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Approval Year

PubMed

Show entries

Title	Date	PubMed
Enhanced enzyme activity and enantioselectivity of lipases in organic solvents by crown ethers and cyclodextrins.	2003	16233437
Newly isolated Streptomyces spp. as enantioselective biocatalysts: hydrolysis of 1,2-O-isopropylidene glycerol racemic esters.	2005	16162249
Enhancement of enzyme activity and enantioselectivity by cyclopentyl methyl ether in the transesterification catalyzed by Pseudomonas cepacia lipase co-lyophilized with cyclodextrins.	2005 Mar	15834802
Fourier transform near-infrared vibrational circular dichroism used for on-line monitoring the epimerization of 2,2-dimethyl-1,3-dioxolane-4-methanol: A pseudo racemization reaction.	2006 Nov	16906494
Organic solvents as vehicles for precipitating liquid embolics: a comparative angiotoxicity study with superselective injections of swine rete mirabile.	2006 Oct	17032862

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Name

Type

Language

SOLKETAL

Common Name

English

ISOPROPYLIDENE GLYCEROL

Systematic Name

English

GLYCEROL ACETONIDE

Systematic Name

English

ISOPROPYLIDENE GLYCEROL [MI]

Common Name

English

ACETONE GLYCERIN KETAL

Common Name

English

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Classification Tree

Code System

Code

SOLVENT CARRIER

Food Contact Sustance Notif, (FCN No.)

FCN NO. 1149

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Code System

Code

Type

Description

FDA UNII

3XK098O8ZW

PRIMARY

SMS_ID

100000092830

PRIMARY

EPA CompTox

DTXSID9021845

PRIMARY

CAS

100-79-8

PRIMARY

DAILYMED

3XK098O8ZW

PRIMARY

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SUBSTANCE RECORD


					3XK098O8ZW

SOLKETAL

SMILES

InChI

Approval Year

PubMed

Patents