442328
2,6-二甲基苯酚
analytical standard
别名:
2-羟基间二甲苯, 连间二甲苯酚
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关于此项目
线性分子式:
(CH3)2C6H3OH
化学文摘社编号:
分子量:
122.16
EC Number:
209-400-1
UNSPSC Code:
12352200
PubChem Substance ID:
Beilstein/REAXYS Number:
1446677
MDL number:
InChI key
NXXYKOUNUYWIHA-UHFFFAOYSA-N
InChI
1S/C8H10O/c1-6-4-3-5-7(2)8(6)9/h3-5,9H,1-2H3
SMILES string
Cc1cccc(C)c1O
grade
analytical standard
autoignition temp.
1110 °F
packaging
ampule of 1000 mg
technique(s)
HPLC: suitable, gas chromatography (GC): suitable
bp
203 °C (lit.)
mp
43-45 °C (lit.)
application(s)
agriculture
environmental
format
neat
storage temp.
room temp
Gene Information
human ... GABRA1(2554)
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Application
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
signalword
Danger
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Aquatic Chronic 2 - Eye Dam. 1 - Skin Corr. 1B - STOT SE 3
target_organs
Respiratory system
存储类别
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
wgk
WGK 3
flash_point_f
186.8 °F - closed cup
flash_point_c
86 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges, type P3 (EN 143) respirator cartridges
法规信息
危险化学品
此项目有
Tingting Li et al.
Talanta, 78(4-5), 1497-1502 (2009-04-14)
In the present work, a simple, selective, and sensitive method has been proposed for the determination of four phenols (catechol, resorcinol, 2,6-dimethylphenol, and 2,4,6-trinitrophenol) in water samples. The method is based on poly-(methacrylic acid-co-ethylene glycol dimethacrylate) monolith microextraction (PMME) and
E A Kemeleva et al.
Bioorganicheskaia khimiia, 34(4), 558-569 (2008-08-13)
Three new sulfur-containing derivatives of 2,6-dimethylphenol were synthesized. Their antioxidative activity, mutagenicity, and genotoxicity were examined by bacterial tests and by calculating the dominant lethal mutations in murine embryonic cells. It was shown that all the compounds synthesized have a
Gertrud Haeseler et al.
British journal of pharmacology, 145(7), 916-925 (2005-05-25)
Phenol derivatives constitute a family of neuroactive compounds. The aim of our study was to identify structural features that determine their modulatory effects at glycine receptors. We investigated the effects of four methylated phenol derivatives and two halogenated analogues on
O Grech-Bélanger et al.
Research communications in chemical pathology and pharmacology, 58(1), 53-62 (1987-10-01)
A new metabolite, 2,6-dimethylphenol obtained by O-dealkylation of mexiletine by rabbit liver was identified. A g.c.-f.i.d. method was developed for its analysis in hepatic homogenates and some of the characteristics of the metabolic reaction were studied. Formation of 2,6-dimethylphenol is
Tarek S Belal et al.
Journal of AOAC International, 91(4), 720-730 (2008-08-30)
Four simple, rapid, sensitive, and selective analytical procedures were developed for determination of mexiletine hydrochloride (MX) and/or its related substance: 2,6-dimethylphenol (DMP). The latter is a synthetic impurity for which a maximum pharmacopeial limit is defined. The first method depends
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