Glycidol

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 Search

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

Title	Date	PubMed
Examination of low-incidence brain tumor responses in F344 rats following chemical exposures in National Toxicology Program carcinogenicity studies.	1999 Sep-Oct	10528639
A convenient chiron for substituted cyclohexanones.	2001 Aug 24	11511271
Expedient access to the okadaic acid architecture: a novel synthesis of the C1-C27 domain.	2001 Feb 9	11430115
Synthesis of the C1-C12 fragment of fostriecin.	2001 Jul 12	11440587
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	11397402
Interpreting the signal from a localized fluorescence sensor: a study by angle-resolved XPS and dynamic SIMS.	2003 Jun 15	16256643
Basis set and density functional dependence of vibrational Raman optical activity calculations.	2005 Aug 25	16834126
Hydrophilic core-shell microspheres: a suitable support for controlled attachment of proteins and biomedical diagnostics.	2005 Dec 15	16294370
Poly(amidoamine) dendrimer-based multifunctional engineered nanodevice for cancer therapy.	2005 Sep 22	16161993
Chemical variation of natural product-like scaffolds: design and synthesis of spiroketal derivatives.	2006 May 21	16688343
Biocatalytic approaches to optically active beta-blockers.	2007	17266567
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	17518441
Oxiranylmethyloxy or thiiranylmethyloxy-azaxanthones and -acridone analogues as potential topoisomerase I inhibitors.	2009 Dec 1	19836231
Enzymatic one-pot route to telechelic polypentadecalactone epoxide: synthesis, UV curing, and characterization.	2009 Nov 9	19807145
A new analytical method for the quantification of glycidol fatty acid esters in edible oils.	2010	20103980
Substrate-controlled asymmetric total synthesis and structure revision of (+)-itomanallene A.	2010	20029867
Significant changes in the transesterification activity of free and mesoporous-immobilized Rhizopus oryzae lipase in ionic liquids.	2010 Feb 1	19948194
A spectroscopic and computational investigation of the conformational structural changes induced by hydrogen bonding networks in the glycidol-water complex.	2010 Jan 14	19904907
Hyperbranched polyglycerols: from the controlled synthesis of biocompatible polyether polyols to multipurpose applications.	2010 Jan 19	19785402

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

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Name

Type

Language

NSC-46096

Preferred Name

English

Glycidol

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