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D175005

2,6-Dimethylphenol

Name: 2,6-Dimethylphenol
Brand: ALDRICH

99%

Synonym(s):

2-Hydroxy-m-xylene, vic.-m-Xylenol

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About This Item

Linear Formula:

(CH₃)₂C₆H₃OH

CAS Number:

576-26-1

Molecular Weight:

122.16

EC Number:

209-400-1

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24893533

Beilstein/REAXYS Number:

1446677

MDL number:

MFCD00002240

Assay:

99%

Form:

powder

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Properties

Quality Level

100

assay

99%

form

powder

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)

Description

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pictograms

GHS06,GHS05,GHS09

signalword

Danger

hcodes

H301 + H311,H314,H335,H411

pcodes

P260 - P273 - P280 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338

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

Storage Class

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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Modified Jeener solid-echo pulse sequences for the measurement of the proton dipolar spin-lattice relaxation time (T1D) of tissue solid-like macromolecular components.

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

Tropospheric multiphase chemistry of 2,5- and 2,6-dimethylphenols: determination of the mass accommodation coefficients and the Henry's law constants.

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

Structural features of phenol derivatives determining potency for activation of chloride currents via alpha(1) homomeric and alpha(1)beta heteromeric glycine receptors.

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

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