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W324906

Sigma-Aldrich

2,6-Xylenol

≥99%, FG

Synonym(s):

2,6-Dimethylphenol, 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
FEMA Number:
3249
Beilstein:
1446677
EC Number:
209-400-1
Council of Europe no.:
11261
MDL number:
MFCD00002240
UNSPSC Code:
12164502
PubChem Substance ID:
24901585
Flavis number:
4.042
NACRES:
NA.21

biological source

synthetic

Quality Level

400

grade

FG
Fragrance grade
Halal

Agency

follows IFRA guidelines
meets purity specifications of JECFA

reg. compliance

EU Regulation 1223/2009
EU Regulation 1334/2008 & 178/2002

Assay

≥99%

autoignition temp.

1110 °F

bp

203 °C (lit.)

mp

43-45 °C (lit.)

application(s)

flavors and fragrances

Documentation

see Safety & Documentation for available documents

food allergen

no known allergens

fragrance allergen

no known allergens

Organoleptic

medicinal

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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Application


  • Methodological Considerations of the Acetaminophen Detection : This study explores the use of 2,6-Xylenol in the detection of acetaminophen through the indophenol reaction, highlighting its importance in forensic science and toxicology for accurate drug testing (Shinkawa et al., 2023).

  • Carbon Dioxide Solubility in Nonionic Deep Eutectic Solvents Containing Phenolic Alcohols: Investigates the solubility of CO2 in solvents containing 2,6-Xylenol, underscoring its potential in capturing and storing carbon dioxide, which is vital for combating climate change (Alhadid et al., 2022).

Signal Word

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 Code

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

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
SHBS2758
SHBR0097
SHBQ1636
STBK0173
STBJ7900

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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
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
J Hartung et al.
Zentralblatt fur Bakteriologie, Mikrobiologie und Hygiene. 1. Abt. Originale B, Hygiene, 179(5), 431-439 (1984-10-01)
Dust-borne phenols and indols were extracted by ethanol from the sedimentation dust of two pig houses (finishing pigs on half slatted floor resp. piglets on deep litter) and a hen house (3-stage battery cages) and analysed by gas chromatography. In
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
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
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