ANTIMONY GLYCOLATE

[OH-].[Sb+3].OCC([O-])=O.OCC([O-])=O

InChIKey=WYOFTXWVYIGTCT-UHFFFAOYSA-K

InChI=1S/2C2H4O3.H2O.Sb/c2*3-1-2(4)5;;/h2*3H,1H2,(H,4,5);1H2;/q;;;+3/p-3

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Substance Class	Chemical Created by `admin` on `Mon Mar 31 23:30:02 GMT 2025` Edited by `admin` on `Mon Mar 31 23:30:02 GMT 2025`
Record UNII	85159IV23A
Record Status	`Validated (UNII)`
Record Version

Name

Type

Language

ANTIMONY, HYDROXYBIS(HYDROXYACETATO(2-)-O1,O2)-

Preferred Name

English

ANTIMONY GLYCOLATE

Systematic Name

English

1,4,6,9-TETRAOXA-5.LAMBDA.5-STIBASPIRO(4.4)NONANE-2,7-DIONE, 5-HYDROXY-

Systematic Name

English

Code System Code Type Description

EPA CompTox

DTXSID101217217

Created by admin on Mon Mar 31 23:30:02 GMT 2025 , Edited by admin on Mon Mar 31 23:30:02 GMT 2025

PRIMARY

CAS

38057-02-2

Created by admin on Mon Mar 31 23:30:02 GMT 2025 , Edited by admin on Mon Mar 31 23:30:02 GMT 2025

PRIMARY

PUBCHEM

118796419

Created by admin on Mon Mar 31 23:30:02 GMT 2025 , Edited by admin on Mon Mar 31 23:30:02 GMT 2025

PRIMARY

FDA UNII

85159IV23A

Created by admin on Mon Mar 31 23:30:02 GMT 2025 , Edited by admin on Mon Mar 31 23:30:02 GMT 2025

PRIMARY