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Merck
CN

442328

2,6-Dimethylphenol

analytical standard

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:
12352200
PubChem Substance ID:
24867802
Beilstein/REAXYS Number:
1446677
MDL number:
MFCD00002240

Key Documents

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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

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

Regulatory Information

危险化学品
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Certificates of Analysis (COA)

Lot/Batch Number
LC25261V
LC23965V
LC08526V
LB98851V
LB86104V

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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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