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Details

Stereochemistry RACEMIC
Molecular Formula C4H10O3
Molecular Weight 106.1204
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 1,2,4-BUTANETRIOL

SMILES

OCCC(O)CO

InChI

InChIKey=ARXKVVRQIIOZGF-UHFFFAOYSA-N
InChI=1S/C4H10O3/c5-2-1-4(7)3-6/h4-7H,1-3H2

HIDE SMILES / InChI

Molecular Formula C4H10O3
Molecular Weight 106.1204
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

PubMed

PubMed

TitleDatePubMed
Six-membered cyclic sulfites derived from glucofuranose and 1,2,4-butanetriol.
2001
Microbial synthesis of the energetic material precursor 1,2,4-butanetriol.
2003 Oct 29
Measurement of serum total glycerides and free glycerol by high-performance liquid chromatography.
2006 Sep
Impact of nature and length of linker incorporated in agonists on toll-like receptor 9-mediated immune responses.
2010 May 13
Patents

Patents

Substance Class Chemical
Created
by admin
on Sat Dec 16 10:55:01 GMT 2023
Edited
by admin
on Sat Dec 16 10:55:01 GMT 2023
Record UNII
NK798C370H
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
1,2,4-BUTANETRIOL
Systematic Name English
NSC-60197
Code English
2-DEOXYERYTHRITOL
Systematic Name English
TRIOL 124
Common Name English
1,3,4-BUTANETRIOL
Systematic Name English
1,2,4-TRIHYDROXYBUTANE
Systematic Name English
(±)-1,2,4-BUTANETRIOL
Systematic Name English
Code System Code Type Description
PUBCHEM
18302
Created by admin on Sat Dec 16 10:55:02 GMT 2023 , Edited by admin on Sat Dec 16 10:55:02 GMT 2023
PRIMARY
ECHA (EC/EINECS)
221-323-5
Created by admin on Sat Dec 16 10:55:01 GMT 2023 , Edited by admin on Sat Dec 16 10:55:01 GMT 2023
PRIMARY
WIKIPEDIA
1,2,4-Butanetriol
Created by admin on Sat Dec 16 10:55:02 GMT 2023 , Edited by admin on Sat Dec 16 10:55:02 GMT 2023
PRIMARY
CAS
3068-00-6
Created by admin on Sat Dec 16 10:55:01 GMT 2023 , Edited by admin on Sat Dec 16 10:55:01 GMT 2023
PRIMARY
NSC
60197
Created by admin on Sat Dec 16 10:55:02 GMT 2023 , Edited by admin on Sat Dec 16 10:55:02 GMT 2023
PRIMARY
EPA CompTox
DTXSID8044416
Created by admin on Sat Dec 16 10:55:01 GMT 2023 , Edited by admin on Sat Dec 16 10:55:01 GMT 2023
PRIMARY
FDA UNII
NK798C370H
Created by admin on Sat Dec 16 10:55:01 GMT 2023 , Edited by admin on Sat Dec 16 10:55:01 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE