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D174602

Sigma-Aldrich

2,5-Dimethylphenol

≥99%

Sinônimo(s):

2-Hydroxy-p-xylene, p-Xylenol

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About This Item

Fórmula linear:
(CH3)2C6H3OH
Número CAS:
Peso molecular:
122.16
Beilstein:
1099260
Número CE:
Número MDL:
Código UNSPSC:
12352100
ID de substância PubChem:
NACRES:
NA.22

Ensaio

≥99%

forma

crystals

pb

212 °C (lit.)

pf

75-77 °C

cadeia de caracteres SMILES

Cc1ccc(C)c(O)c1

InChI

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

chave InChI

NKTOLZVEWDHZMU-UHFFFAOYSA-N

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Categorias relacionadas

Aplicação

  • 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).

Palavra indicadora

Danger

Frases de perigo

Classificações de perigo

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

Código de classe de armazenamento

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

Classe de risco de água (WGK)

WGK 3

Equipamento de proteção individual

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


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B J Day et al.
Research communications in chemical pathology and pharmacology, 76(1), 117-120 (1992-04-01)
Pulmonary metabolites of p-xylene, p-methylbenzyl alcohol (PMBA) and 2,5-dimethylphenol (DMP), were employed to investigate the divergent effects of p-xylene on pulmonary and hepatic metabolism. Rats were given PMBA, DMP, or 10% cremophore (control) ip daily for 3 days, and effects
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)
G Bieniek
Occupational and environmental medicine, 51(5), 354-356 (1994-05-01)
Phenol (87.3 mg/l), p-cresol (58.6 mg/l), o-cresol (76.9 mg/l), and 2,5-xylenol (36.7 mg/l) were detected in the urine of workers employed in the distillation of the high temperature phenolic fraction of tar (carbolic oil). The concentrations of these compounds in

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