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D174203

Sigma-Aldrich

2,4-Dimethylphenol

98%

Synonym(s):

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

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About This Item

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

vapor pressure

0.1 mmHg ( 25 °C)

Quality Level

100

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.)

SMILES string

Cc1ccc(O)c(C)c1

InChI

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

InChI key

KUFFULVDNCHOFZ-UHFFFAOYSA-N

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Signal Word

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 Code

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

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
SHBP0214
SHBN5792
SHBN3898
SHBM6867
SHBM6311

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2,6-Dimethylphenol ≥99.5%

Sigma-Aldrich

D174904

2,6-Dimethylphenol

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
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 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
Arturo Romero et al.
Journal of hazardous materials, 162(2-3), 785-790 (2008-07-08)
Hydrogen peroxide has been used to oxidize a sorbed aromatic contaminant in a loamy sand with 195.9 g kg(-1) of organic carbon by using iron as catalyst at 20 degrees C. The 2,4-dimethylphenol (2,4-DMP) was chosen as pollutant. Because of
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