99500-87-5

Basic information

• Product Name: 1-(2,4-dimethylphenyl)ethanol
• Synonyms: 1-(2,4-Dimethylphenyl)ethan-1-ol; 1-(2,4-Dimethylphenyl)ethanol; 5379-19-1; alpha,2,5-Trimethylbenzenemethanol; Benzenemethanol, alpha,2,4-trimethyl-
• CAS NO: 99500-87-5
• Molecular Formula: C₁₀H₁₄O
• Molecular Weight: 150.2176
• Mol File: 99500-87-5.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 225.8°C at 760 mmHg
• Flash Point: 100°C
• Density: 0.981g/cm³
• Vapor Pressure: 0.048mmHg at 25°C
• Refractive Index: 1.526
• CAS DataBase Reference: 1-(2,4-dimethylphenyl)ethanol(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(2,4-dimethylphenyl)ethanol(99500-87-5)
• EPA Substance Registry System: 1-(2,4-dimethylphenyl)ethanol(99500-87-5)

Safety Data

• Hazardous Substances Data: 99500-87-5(Hazardous Substances Data)

Usage

Description

1-(2,4-Dimethylphenyl)ethanol, also known as 2,4-Xylenol ethanol, is a chemical compound with the molecular formula C10H14O. It is a colorless, viscous liquid that is characterized by its pleasant odor and antimicrobial properties.

Uses

Used in Fragrance and Flavor Industry:
1-(2,4-Dimethylphenyl)ethanol is used as a fragrance and flavoring agent for its pleasant odor, making it suitable for the production of perfumes, soaps, and other cosmetic products.
Used in Pharmaceutical and Personal Care Industry:
1-(2,4-Dimethylphenyl)ethanol is used as a disinfectant and preservative in some pharmaceutical and personal care products due to its antimicrobial properties.

Upstream product

• 102877-07-6 1-(2,4-dimethylphenyl)ethanamine 
• 89-74-7 2,4-dimethylacetophenone. 
• 7446-70-0 aluminium trichloride 
• 107-06-2 1,2-dichloro-ethane 
• 75-36-5 acetyl chloride 
• 108-38-3 m-xylene 
• 64-17-5 ethanol 
• 64-19-7 acetic acid 

Downstream Products

• 2234-20-0 2,4-dimethylstyrene 
• 168749-62-0 1-(2,4-Dimethyl-phenyl)-ethanol 
• 166940-44-9 (S)-1-(2,4-dimethylphenyl)ethan-1-ol 
• 166940-44-9 1-(2,4-Dimethyl-phenyl)-ethanol 
• 73195-78-5 1-(1,2-dibromo-ethyl)-2,4-dimethyl-benzene 
• 14679-18-6 2-(o,p-Dimethylphenyl)-aethyl-n-butyl-sulfid 
• 459451-02-6 5-(2-Piperidinyl-ethyl)-2-methyl-1H-indole-3-carboxylic 1-(2,4-dimethylphenyl)-ethyl ester 
• 459451-03-7 5-(2-(4-Hydroxy-piperidino)-ethyl)-2-methyl-1H-indole-3-carboxylic acid 1-(2,4-dimethylphenyl)-ethyl ester 
• 166940-44-9 (R)-1-(2,4-dimethylphenyl)ethan-1-ol 
• 1121050-99-4 C₁₀H₁₃N₃ 
• 1342259-84-0 (R)-1-(2,4-dimethylphenyl)ethyl valerate 
• 1613639-26-1 C₁₃H₁₈O₂ 
• 1019527-08-2 N-(1-(2,4-dimethylphenyl)ethyl)aniline 
• 20871-92-5 2-(bromoethyl)-5-methyltoluene 

Relevant articles and documents

AZAINDOLE COMPOUNDS, SYNTHESIS THEREOF, AND METHODS OF USING THE SAME

The invention provides compounds of formula (I) and methods of treating a Mycobacterium infection or tuberculosis, or inhibiting DprE1 with the same.

NBu4NI-catalyzed direct synthesis of α-ketoamides from aryl methyl ketones with dialkylformamides in water using TBHP as oxidant

A novel and easy practical direct synthesis of α-ketoamides has been developed without metals in water. This procedure was catalyzed by nBu 4NI using TBHP as oxidant from simple substrates, aryl methyl ketones and dialkylformamides. The Royal Society of Chemistry 2012.

Dimethylbenzene derivatives

Compounds of the formula (I): wherein X is a —(C═CH2)— group or a —CH(CH3)— group, with the proviso that when X is a —(C═CH2)— group, R1 is a C1-10 alkyl group or a C2-10 alkenyl group and