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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)

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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Related Categories

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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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2,6-Dimethylphenol ≥99.5%

Sigma-Aldrich

D174904

2,6-Dimethylphenol

Peipei Qi et al.
Talanta, 81(4-5), 1630-1635 (2010-05-06)
A molecularly imprinted polymer (MIP) was prepared using 2,4-dimethylphenol (2,4-DMP) as template. The synthesis is optimized by using three different porogens, chloroform, acetonitrile and toluene. The MIP was used as a class-selective sorbent in molecularly imprinted solid-phase extraction (MIP-SPE) for
Metabolism and distribution of 2,4-dimethylphenol in rat.
J S Kaka et al.
Ecotoxicology and environmental safety, 6(1), 35-40 (1982-02-01)
C C Agee et al.
Antimicrobial agents and chemotherapy, 18(2), 243-248 (1980-08-01)
Mycoplasma pneumoniae induces pneumonia-like symptoms in hamsters and causes ciliostasis and cytonecrosis in hamster tracheal explants. 2,4-Dimethylphenol and, to a lesser extent, its 2,3-, 2,5-, and 2,6-dimethylphenol isomers protected tracheal explants from these changes after exposure to virulent M. pneumoniae
B Bukowska et al.
Biochemistry and molecular biology international, 45(1), 47-59 (1998-06-23)
The effect of phenoxyherbicides and their metabolites on the structure of oxy- and deoxyhemoglobin was studied by using different doses and times of incubation of hemoglobin with the herbicide. It was ascertained that among the investigated hemoglobins the most sensitive
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
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