| Weight | 106.121 g/mol |
|---|---|
| Formula | C4H10O3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 3 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 3 |
1,2,4-BUTANETRIOL (3068-00-6)
Score:
#10 in Biotechnology
,
#7068 in Chemistry
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- Catalytic Asymmetric Aminolysis of 3,5,8-Trioxabicyclo[5.1.0]octane Providing an Optically Pure 2-Amino-1,3,4-butanetriol Equivalent. (Journal of Organic Chemistry, 1999)
- Microbial Synthesis of the Energetic Material Precursor 1,2,4-Butanetriol (Journal of the American Chemical Society, 2003)
- Facile access to (S)-1,2,4-butanetriol and its derivatives (Canadian Journal of Chemistry, 1984)
- GroESL overexpression imparts Escherichia coli tolerance to i-, n-, and 2-butanol, 1,2,4-butanetriol and ethanol with complex and unpredictable patterns (Metabolic Engineering, 2013)
- On the formation of the 1,2-acetonide of (+), (), and () 1,2,4-butanetriol and its corresponding aldehyde (Tetrahedron Letters, 1982)
- Synthesis of cationic lipids from 1,2,4-butanetriol (Tetrahedron Letters, 1999)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC(CO)C(CO)O
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InChIKeyARXKVVRQIIOZGF-UHFFFAOYSA-N
- Pubchem - 1,2,4-BUTANETRIOL
- Wikipedia - 1,2,4-butanetriol
1,2,4-Butanetriol is a clear or slightly yellow, odorless, hygroscopic, flammable, viscous liquid. It is an alcohol with three hydrophilic alcoholic hydroxyl groups. It is similar to glycerol and erythritol.
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1 alternate name
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(628-99-9)
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1 alternate name
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3 suppliers
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(111-32-0)
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(30899-19-5, 71-41-0)
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1 alternate name
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1 alternate name
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1,2,4-BUTANETRIOL
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