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Fórmula lineal:
(CH3)2C6H3OH
Número CAS:
Peso molecular:
122.16
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
209-400-1
Beilstein/REAXYS Number:
1446677
MDL number:
Assay:
≥99.5%
Form:
crystals
Servicio técnico
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Permítanos ayudarleQuality Level
assay
≥99.5%
form
crystals
autoignition temp.
1110 °F
bp
203 °C (lit.)
mp
43-45 °C (lit.)
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)
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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
Clase de almacenamiento
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
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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
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
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


