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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:
209-400-1
Beilstein/REAXYS Number:
1446677
MDL number:
Assay:
99%
Form:
powder
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
assay
99%
form
powder
autoignition temp.
1110 °F
bp
203 °C (lit.)
mp
43-45 °C (lit.)
Quality Level
Gene Information
human ... GABRA1(2554)
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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
Pascal Diévart et al.
Physical chemistry chemical physics : PCCP, 8(14), 1714-1723 (2006-04-25)
The uptake of 2,5-dimethylphenol and 2,6-dimethylphenol on aqueous surfaces was measured between 279 and 293 K, using the wetted-wall flow tube technique coupled with UV absorption spectroscopic detection. For both compounds, the uptake coefficients gamma were found to be independent
Measurement of detergent concentration using 2,6-dimethylphenol in membrane-protein crystallization.
Chelsy Prince et al.
Acta crystallographica. Section D, Biological crystallography, 68(Pt 12), 1694-1696 (2012-11-16)
Methods have previously been developed to measure detergent concentration in membrane-protein samples, but most have significant limitations, such as requiring specialized equipment or consuming a significant amount of precious sample. This work explores the use of 2,6-dimethylphenol in a phenol-sulfuric
M Altamirano et al.
Journal of colloid and interface science, 270(2), 364-370 (2003-12-31)
The luminescence properties of tris(1,2-bipyridine)ruthenium(II) (Ru(bpy)(3)(2+)), included in different organically modified silicate gel matrixes were investigated. Spin and dip-coated thin films were prepared from methyltrimethoxysilane (MTMOS) and methyltriethoxysilane (MTEOS). A blue shift in the emission spectrum of the MLCT excited
B Mohammadi et al.
European journal of pharmacology, 421(2), 85-91 (2001-06-12)
Propofol directly activates gamma-aminobutyric acid (GABA(A)) receptors in the absence of the natural agonist. This mechanism is supposed to contribute to its sedative-hypnotic actions. We studied the effects of seven structurally related phenol derivatives on chloride inward currents via rat
Gertrud Haeseler et al.
British journal of pharmacology, 137(2), 285-293 (2002-09-05)
1. The structural features that determine the state-dependent interaction of local anaesthetics with voltage-operated sodium channels are still a matter of debate. We have studied the blockade of sodium channels by 2,6-dimethylphenol, a phenol derivative which resembles the aromatic tail
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