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
SMILES
OCCC(O)CO
InChI
InChIKey=ARXKVVRQIIOZGF-UHFFFAOYSA-N
InChI=1S/C4H10O3/c5-2-1-4(7)3-6/h4-7H,1-3H2
| 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
| Title | Date | PubMed |
|---|---|---|
| Solubility enhancement of Cox-2 inhibitors using various solvent systems. | 2003 |
|
| Production of optically active 1,2,4-butanetriol from corresponding racemate by Microbial stereoinversion. | 2007 May |
|
| Impact of nature and length of linker incorporated in agonists on toll-like receptor 9-mediated immune responses. | 2010 May 13 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 10:55:01 GMT 2023
by
admin
on
Sat Dec 16 10:55:01 GMT 2023
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| Record UNII |
NK798C370H
|
| Record Status |
Validated (UNII)
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| Record Version |
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| Code System | Code | Type | Description | ||
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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
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221-323-5
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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
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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
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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
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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
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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
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PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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ENANTIOMER -> RACEMATE | |||
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ENANTIOMER -> RACEMATE |
