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Merck
CN

D174602

2,5-Dimethylphenol

≥99%

Synonym(s):

2-Hydroxy-p-xylene, p-Xylenol

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About This Item

Linear Formula:
(CH3)2C6H3OH
CAS Number:
Molecular Weight:
122.16
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-461-5
Beilstein/REAXYS Number:
1099260
MDL number:
Assay:
≥99%
Form:
crystals
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Quality Level

assay

≥99%

form

crystals

bp

212 °C (lit.)

mp

75-77 °C

SMILES string

Cc1ccc(C)c(O)c1

InChI

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

InChI key

NKTOLZVEWDHZMU-UHFFFAOYSA-N

Application

  • Fungicide Metabolism in Wheat: 2,5-Dimethylphenol, a breakdown product of the strobilurin fungicide mandestrobin, was studied for its metabolic pathways in wheat. This research provides insights into the environmental behavior and safety of pesticide residues in agricultural products (Ando et al., 2018).
  • Tropospheric Chemistry of Dimethylphenols: The study on the mass accommodation coefficients and Henry′s law constants of 2,5-dimethylphenol underlines its significant atmospheric reactions, contributing to a better understanding of air quality and environmental chemistry (Diévart et al., 2006).


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Danger

Hazard Classifications

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

Storage Class

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

wgk

WGK 3

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

Regulatory Information

危险化学品

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C C Yeo et al.
Microbiology (Reading, England), 143 ( Pt 8), 2833-2840 (1997-08-01)
Pseudomonas alcaligenes NCIB 9867 (strain P25X), which grows on 2,5-xylenol and harbours the plasmid RP4, was mated with a plasmid-free derivative of Pseudomonas putida NCIB 9869, strain RA713, which cannot grow on 2,5-xylenol. Some RA713 transconjugants, initially selected on 2,5-xylenol
Chew Chieng Yeo et al.
Gene, 312, 239-248 (2003-08-12)
Pseudomonas alcaligenes NCIMB 9867 (strain P25X) produces isofunctional enzymes of the gentisate pathway that enables the degradation of xylenols and cresols via gentisate. Previous reports had indicated that one set of enzymes is constitutively expressed whereas the other set is
Separation and determination of phenol, alpha-naphthol m- and p-, o-cresols and 2,5-xylenol, and catechol in the urine after mixed exposure to phenol, naphthalene, cresols, and xylenols.
G Bieniek et al.
British journal of industrial medicine, 43(8), 570-571 (1986-08-01)



Global Trade Item Number

SKUGTIN
D174602-100G04061833560600
D174602-5G04061833560617