CAS 18299-15-5

4-HYDROXY-3-METHYLBENZYL ALCOHOL

Description:

4-Hydroxy-3-methylbenzyl alcohol, with the CAS number 18299-15-5, is an organic compound characterized by its aromatic structure, which includes a hydroxyl group (-OH) and a methyl group (-CH3) attached to a benzyl alcohol framework. This compound typically appears as a colorless to pale yellow liquid or solid, depending on its purity and form. It is soluble in organic solvents and exhibits moderate solubility in water due to the presence of the hydroxyl group, which can engage in hydrogen bonding. The compound is known for its potential applications in the fragrance and cosmetic industries, as well as in the synthesis of other organic compounds. Its chemical properties include the ability to undergo typical reactions of alcohols, such as oxidation and esterification. Additionally, it may exhibit antioxidant properties, making it of interest in various formulations. Safety data should be consulted for handling and exposure guidelines, as with any chemical substance.

Formula: C₈H₁₀O₂

Synonyms:

• Rarechem Al Bd 0693

Benzenemethanol, 4-hydroxy-3-methyl-

CAS: 18299-15-5

Formula: C₈H₁₀O₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 138.1638

Ref: IN-DA0024BB

4-(Hydroxymethyl)-2-methylphenol

CAS: 18299-15-5

4-(Hydroxymethyl)-2-methylphenol

Purity: 97%

Molecular weight: 138.16g/mol

Ref: 54-OR81242

4-(Hydroxymethyl)-2-methylphenol

CAS: 18299-15-5

Formula: C₈H₁₀O₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 138.166

Ref: 10-F215009

4-Hydroxy-3-methylbenzyl alcohol

CAS: 18299-15-5

4-Hydroxy-3-methylbenzyl alcohol (4MBA) is a natural product that is synthesized from 4-hydroxy-3-methylbenzaldehyde by a nonribosomal peptide synthetase. It has been shown to have an inhibitory effect on the growth of certain bacteria, such as Bacillus subtilis and Escherichia coli. It also inhibits the production of vanillyl alcohol, which is an intermediary metabolite in the biosynthesis of lignin. This compound utilizes energy sources such as glucose, glycerol, and formate for growth. 4MBA has been shown to undergo oxidation reactions with oxygen, nitrate, nitrite, and peroxide to produce benzoic acid derivatives. The gene knockout experiments show that this compound is involved in the utilization of various carbon sources and its specific growth rate is increased by 500%.

Formula: C₈H₁₀O₂

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 138.16 g/mol

Ref: 3D-FH09889