Skip to Content
Merck
CN

D174203

2,4-Dimethylphenol

98%

Synonym(s):

4-Hydroxy-m-xylene, asym.-m-Xylenol

Sign In to View Organizational & Contract Pricing.

Select a Size

About This Item

Linear Formula:
(CH3)2C6H3OH
CAS Number:
105-67-9
Molecular Weight:
122.16
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24893529
EC Number:
203-321-6
Beilstein/REAXYS Number:
636244
MDL number:
MFCD00002233
Assay:
98%
Form:
liquid

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Product Name

2,4-Dimethylphenol, 98%

InChI key

KUFFULVDNCHOFZ-UHFFFAOYSA-N

InChI

1S/C8H10O/c1-6-3-4-8(9)7(2)5-6/h3-5,9H,1-2H3

SMILES string

Cc1ccc(O)c(C)c1

vapor pressure

0.1 mmHg ( 25 °C)

assay

98%

form

liquid

refractive index

n20/D 1.538 (lit.)

bp

211-212 °C (lit.)

mp

22-23 °C (lit.)

density

1.011 g/mL at 25 °C (lit.)

Looking for similar products? Visit Product Comparison Guide

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Aquatic Chronic 2 - Eye Dam. 1 - Skin Corr. 1B - Skin Sens. 1B

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk

WGK 3

flash_point_f

201.2 °F - closed cup

flash_point_c

94.0 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

Regulatory Information

危险化学品
This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
SHBP0214
SHBN5792
SHBN3898
SHBM6867
SHBM6311

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Diversity-oriented synthesis of polycyclic scaffolds by modification of an anodic product derived from 2,4-dimethylphenol.
Joaquin Barjau et al.
Angewandte Chemie (International ed. in English), 50(6), 1415-1419 (2011-02-04)
Hiroko Tsukatani et al.
Analytica chimica acta, 682(1-2), 72-76 (2010-11-09)
Gas chromatography/supersonic jet/resonance-enhanced multiphoton ionization/time-of-flight mass spectrometry (GC/SSJ/REMPI/TOF-MS) was employed for isomer-selective determination of 2,4-xylenol in river and seawater samples. The sample containing 2,4-xylenol was measured using argon, rather than helium, as the GC carrier gas to cool the analyte
J P Ghosh et al.
Chemosphere, 71(9), 1709-1717 (2008-02-13)
The potential use of laccase (SP-504) in an advanced oxidation-based treatment technology to remove 2,4-dimethylphenol (DMP) from water was investigated with and without the additive, polyethylene glycol (PEG). The DMP concentration was varied between 1.0 and 5.0 mM. The optimization
F L Arenghi et al.
Applied and environmental microbiology, 67(7), 3304-3308 (2001-06-27)
Pseudomonas stutzeri OX1 meta pathway genes for toluene and o-xylene catabolism were analyzed, and loci encoding phenol hydroxylase, catechol 2,3-dioxygenase, 2-hydroxymuconate semialdehyde dehydrogenase, and 2-hydroxymuconate semialdehyde hydrolase were mapped. Phenol hydroxylase converted a broad range of substrates, as it was
J Liira et al.
Xenobiotica; the fate of foreign compounds in biological systems, 21(1), 53-63 (1991-01-01)
1. Rats were exposed to m-xylene (300 ppm) and methyl ethyl ketone (MEK, 600 ppm) vapour, separately and in combination. 2. Repeated exposures to m-xylene enhanced liver drug-metabolizing capacity, whereas MEK showed no effects. After mixed exposure the cytochrome P-450-dependent
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service