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线性分子式:
(CH3)2C6H3OH
化学文摘社编号:
分子量:
122.16
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-461-5
Beilstein/REAXYS Number:
1099260
MDL number:
产品名称
2,5-二甲基苯酚, ≥99%
InChI key
NKTOLZVEWDHZMU-UHFFFAOYSA-N
InChI
1S/C8H10O/c1-6-3-4-7(2)8(9)5-6/h3-5,9H,1-2H3
SMILES string
Cc1ccc(C)c(O)c1
assay
≥99%
form
crystals
bp
212 °C (lit.)
mp
75-77 °C
Quality Level
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Application
- 小麦中杀真菌剂的代谢:研究了strobilurin类杀真菌剂mandestrobin的分解产物2,5-二甲基苯酚在小麦中的代谢途径。该研究提供了有关农产品中杀虫剂残留的环境行为和安全性的见解(Ando et al., 2018)。
- 二甲苯酚的对流层化学:该研究考察了2,5-二甲基苯酚的质量容纳系数(mass accommodation coefficient)和亨利常数,强调了其对大气反应的重要性,有助于我们更好地理解空气质量和环境化学(Diévart et al., 2006)。
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Aquatic Chronic 2 - Eye Dam. 1 - Skin Corr. 1B
存储类别
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
法规信息
危险化学品
此项目有
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
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
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
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)
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
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