U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS
This repository is under review for potential modification in compliance with Administration directives.

Details

Stereochemistry RACEMIC
Molecular Formula C3H6O2
Molecular Weight 74.0785
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Glycidol

SMILES

OCC1CO1

InChI

InChIKey=CTKINSOISVBQLD-UHFFFAOYSA-N
InChI=1S/C3H6O2/c4-1-3-2-5-3/h3-4H,1-2H2

HIDE SMILES / InChI

Molecular Formula C3H6O2
Molecular Weight 74.0785
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

PubMed

PubMed

TitleDatePubMed
Examination of low-incidence brain tumor responses in F344 rats following chemical exposures in National Toxicology Program carcinogenicity studies.
1999 Sep-Oct
A convenient chiron for substituted cyclohexanones.
2001 Aug 24
Expedient access to the okadaic acid architecture: a novel synthesis of the C1-C27 domain.
2001 Feb 9
Synthesis of the C1-C12 fragment of fostriecin.
2001 Jul 12
Point mutations of K-ras and H-ras genes in forestomach neoplasms from control B6C3F1 mice and following exposure to 1,3-butadiene, isoprene or chloroprene for up to 2-years.
2001 Jun 1
Interpreting the signal from a localized fluorescence sensor: a study by angle-resolved XPS and dynamic SIMS.
2003 Jun 15
Basis set and density functional dependence of vibrational Raman optical activity calculations.
2005 Aug 25
Hydrophilic core-shell microspheres: a suitable support for controlled attachment of proteins and biomedical diagnostics.
2005 Dec 15
Poly(amidoamine) dendrimer-based multifunctional engineered nanodevice for cancer therapy.
2005 Sep 22
Chemical variation of natural product-like scaffolds: design and synthesis of spiroketal derivatives.
2006 May 21
Biocatalytic approaches to optically active beta-blockers.
2007
Preparation of liquid-core nanocapsules from poly[(ethylene oxide)-co-glycidol] with multiple hydrophobic linoleates at an oil-water interface and its encapsulation of pyrene.
2007 Jun
Oxiranylmethyloxy or thiiranylmethyloxy-azaxanthones and -acridone analogues as potential topoisomerase I inhibitors.
2009 Dec 1
Enzymatic one-pot route to telechelic polypentadecalactone epoxide: synthesis, UV curing, and characterization.
2009 Nov 9
A new analytical method for the quantification of glycidol fatty acid esters in edible oils.
2010
Substrate-controlled asymmetric total synthesis and structure revision of (+)-itomanallene A.
2010
Significant changes in the transesterification activity of free and mesoporous-immobilized Rhizopus oryzae lipase in ionic liquids.
2010 Feb 1
A spectroscopic and computational investigation of the conformational structural changes induced by hydrogen bonding networks in the glycidol-water complex.
2010 Jan 14
Hyperbranched polyglycerols: from the controlled synthesis of biocompatible polyether polyols to multipurpose applications.
2010 Jan 19
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 17:35:22 GMT 2025
Edited
by admin
on Mon Mar 31 17:35:22 GMT 2025
Record UNII
S54CF1DV9A
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-46096
Preferred Name English
Glycidol
HSDB   MI  
Common Name English
DL-GLYCIDOL
Common Name English
LEVODROPROPIZINE IMPURITY C [EP IMPURITY]
Common Name English
GLYCIDOL [IARC]
Common Name English
GLYCIDE
Common Name English
1-HYDROXY-2,3-EPOXYPROPANE
Systematic Name English
2-OXIRANEMETHANOL
Systematic Name English
2,3-EPOXY-1-PROPANOL
Systematic Name English
(±)-GLYCIDOL
Common Name English
1,2-EPOXY-3-HYDROXYPROPANE
Systematic Name English
GLYCIDOL [EP IMPURITY]
Common Name English
GLYCIDOL [HSDB]
Common Name English
(RS)-GLYCIDOL
Common Name English
OXIRANYLMETHANOL
Systematic Name English
D-L-GLYCIDOL
Common Name English
GLYCIDOL [MI]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C45408
Created by admin on Mon Mar 31 17:35:22 GMT 2025 , Edited by admin on Mon Mar 31 17:35:22 GMT 2025
Code System Code Type Description
CAS
556-52-5
Created by admin on Mon Mar 31 17:35:22 GMT 2025 , Edited by admin on Mon Mar 31 17:35:22 GMT 2025
PRIMARY
NCI_THESAURUS
C44387
Created by admin on Mon Mar 31 17:35:22 GMT 2025 , Edited by admin on Mon Mar 31 17:35:22 GMT 2025
PRIMARY
WIKIPEDIA
GLYCIDOL
Created by admin on Mon Mar 31 17:35:22 GMT 2025 , Edited by admin on Mon Mar 31 17:35:22 GMT 2025
PRIMARY
HSDB
1819
Created by admin on Mon Mar 31 17:35:22 GMT 2025 , Edited by admin on Mon Mar 31 17:35:22 GMT 2025
PRIMARY
MERCK INDEX
m5795
Created by admin on Mon Mar 31 17:35:22 GMT 2025 , Edited by admin on Mon Mar 31 17:35:22 GMT 2025
PRIMARY Merck Index
SMS_ID
300000053404
Created by admin on Mon Mar 31 17:35:22 GMT 2025 , Edited by admin on Mon Mar 31 17:35:22 GMT 2025
PRIMARY
EPA CompTox
DTXSID4020666
Created by admin on Mon Mar 31 17:35:22 GMT 2025 , Edited by admin on Mon Mar 31 17:35:22 GMT 2025
PRIMARY
CHEBI
30966
Created by admin on Mon Mar 31 17:35:22 GMT 2025 , Edited by admin on Mon Mar 31 17:35:22 GMT 2025
PRIMARY
FDA UNII
S54CF1DV9A
Created by admin on Mon Mar 31 17:35:22 GMT 2025 , Edited by admin on Mon Mar 31 17:35:22 GMT 2025
PRIMARY
NSC
46096
Created by admin on Mon Mar 31 17:35:22 GMT 2025 , Edited by admin on Mon Mar 31 17:35:22 GMT 2025
PRIMARY
ECHA (EC/EINECS)
209-128-3
Created by admin on Mon Mar 31 17:35:22 GMT 2025 , Edited by admin on Mon Mar 31 17:35:22 GMT 2025
PRIMARY
PUBCHEM
11164
Created by admin on Mon Mar 31 17:35:22 GMT 2025 , Edited by admin on Mon Mar 31 17:35:22 GMT 2025
PRIMARY
MESH
C004312
Created by admin on Mon Mar 31 17:35:22 GMT 2025 , Edited by admin on Mon Mar 31 17:35:22 GMT 2025
PRIMARY
Related Record Type Details
PARENT -> IMPURITY
fatty acid esters of GLYCIDOL also present
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (GC)
EP