CAS 497-06-3

3-Butene-1,2-diol

Description:

3-Butene-1,2-diol, with the CAS number 497-06-3, is an organic compound characterized by its structure, which features a butene backbone with hydroxyl (–OH) groups at the first and second carbon positions. This compound is a diol, indicating the presence of two alcohol functional groups, which contributes to its reactivity and solubility in polar solvents like water. 3-Butene-1,2-diol is typically a colorless liquid at room temperature and exhibits a relatively low boiling point compared to larger alcohols. Its chemical properties include the ability to undergo various reactions such as oxidation and dehydration, making it useful in organic synthesis. Additionally, the presence of the double bond in the butene structure allows for further chemical modifications. Due to its functional groups, 3-butene-1,2-diol can participate in hydrogen bonding, influencing its physical properties such as viscosity and volatility. It is important to handle this compound with care, as it may pose health risks upon exposure, and proper safety protocols should be followed in laboratory settings.

Formula: C₄H₈O₂

InChI: InChI=1S/C4H8O2/c1-2-4(6)3-5/h2,4-6H,1,3H2

InChI key: InChIKey=ITMIAZBRRZANGB-UHFFFAOYSA-N

SMILES: C(C=C)(CO)O

Synonyms:

• 1,2-Dihydroxy-3-butene
• 1-Buten-3,4-diol
• 1-Butene-3,4-diol
• 3,4-Dihydroxy-1-Butene
• But-3-Ene-1,2-Diol
• But-3-en-1,2-diol
• Erythrol
• 3-Butene-1,2-diol

3-Butene-1,2-diol

CAS: 497-06-3

Formula: C₄H₈O₂

Purity: 98%

Color and Shape: Liquid

Molecular weight: 88.1051

Ref: IN-DA0032QG

3-Butene-1,2-Diol

CAS: 497-06-3

3-Butene-1,2-Diol

Purity: 98%

Molecular weight: 88.11g/mol

Ref: 54-OR1010942

1-Butene-3,4-diol

CAS: 497-06-3

1-Butene-3,4-diol is a reactive compound that is used in analytical methods. It can be synthesized by an asymmetric synthesis from 1,2-butanediol. This product has been shown to inhibit aminotransferase activity in rat liver microsomes and to be metabolized through the cytochrome P450 system. 1-Butene-3,4-diol also inhibits polymerase chain reactions and is reactive with hydrochloric acid. It may cause fatty acid metabolism and hydroxyl group formation.

Formula: C₄H₈O₂

Purity: Min. 95%

Color and Shape: Colorless Clear Liquid

Molecular weight: 88.11 g/mol

Ref: 3D-FB19379

3-Butene-1,2-diol

CAS: 497-06-3

Formula: C₄H₈O₂

Purity: 95%

Color and Shape: Liquid

Molecular weight: 88.106

Ref: 10-F099464

1-Butene-3,4-diol

Controlled Product

CAS: 497-06-3

Applications Decomposition product of Erythritol.
References Minerath, E., et al.: Environ. Sci. Technol., 43, 8133 (2009), Barshteyn, N., et al.: Chem. Res. Toxicol., 22, 1163 (2009), Filser, J., et al.: Toxicol. Sci., 114, 25 (2010),

Formula: C₄H₈O₂

Color and Shape: Neat

Molecular weight: 88.11

Ref: TR-B690165