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:
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
SMILES string
Cc1cccc(C)c1O
InChI
1S/C8H10O/c1-6-4-3-5-7(2)8(6)9/h3-5,9H,1-2H3
InChI key
NXXYKOUNUYWIHA-UHFFFAOYSA-N
Gene Information
human ... GABRA1(2554)
Application
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
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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
[Changes in the erythrocyte osmotic resistance of rats as affected by 2,6-dimethylphenol in vivo and in vitro].
Iu M Konstantinov et al.
Gigiena i sanitariia, (10)(10), 64-64 (1982-10-01)
H Yang et al.
Journal of magnetic resonance. Series B, 105(3), 205-210 (1994-11-01)
Modified Jeener solid-echo pulse sequences are proposed for the measurement of the proton dipolar spin-lattice relaxation time, T1D, of motionally restricted (solid-like) components in the presence of mobile molecular species, such as encountered in biological tissue. A phase-cycled composite-pulse sequence
M Hofrichter et al.
Journal of basic microbiology, 35(5), 303-313 (1995-01-01)
o-Cresol induced glucose-grown resting mycelia of Penicillium frequentans Bi 7/2 (ATCC-number: 96048) immediately oxidized o-cresol and other phenols. After precultivation on glucose and phenol degradation started after a lag-phase of 24 hours. Metabolites of o-cresol metabolism were methylhydroquinone, methyl-p-benzoquinone, 2-methyl-5-hydroxyhydroquinone