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W324906

Sigma-Aldrich

2,6-Xylenol

≥99%, FG

Sinônimo(s):

2,6-Dimethylphenol, 2-Hydroxy-m-xylene, vic.-m-Xylenol

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About This Item

Fórmula linear:
(CH3)2C6H3OH
Número CAS:
576-26-1
Peso molecular:
122.16
Número FEMA:
3249
Beilstein:
1446677
Número CE:
209-400-1
Conselho da Europa nº:
11261
Número MDL:
MFCD00002240
Código UNSPSC:
12164502
ID de substância PubChem:
24901585
Número de Flavis:
4.042
NACRES:
NA.21

fonte biológica

synthetic

grau

FG
Fragrance grade
Halal

Agency

follows IFRA guidelines
meets purity specifications of JECFA

conformidade reg.

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

Ensaio

≥99%

temperatura de autoignição

1110 °F

p.e.

203 °C (lit.)

pf

43-45 °C (lit.)

aplicação(ões)

flavors and fragrances

Documentação

see Safety & Documentation for available documents

alérgeno alimentar

no known allergens

alérgeno de fragrância

no known allergens

Organoléptico

medicinal

cadeia de caracteres SMILES

Cc1cccc(C)c1O

InChI

1S/C8H10O/c1-6-4-3-5-7(2)8(6)9/h3-5,9H,1-2H3

chave InChI

NXXYKOUNUYWIHA-UHFFFAOYSA-N

Informações sobre genes

human ... GABRA1(2554)

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Aplicação


  • 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).

Palavra indicadora

Danger

Classificações de perigo

Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Aquatic Chronic 2 - Eye Dam. 1 - Skin Corr. 1B - STOT SE 3

Órgãos-alvo

Respiratory system

Código de classe de armazenamento

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

186.8 °F - closed cup

Ponto de fulgor (°C)

86 °C - closed cup

Equipamento de proteção individual

dust mask type N95 (US), Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges, type P3 (EN 143) respirator cartridges

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Certificados de análise (COA)

Lot/Batch Number
STBK0173
STBJ7900
STBJ6700
STBJ0714
STBH8789

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Heparin sodium porcine mucosa

L Puig-Grajales et al.
Applied microbiology and biotechnology, 54(5), 692-697 (2000-12-29)
Alkylphenols and fuel oxygenates are important environmental pollutants produced by the petrochemical industry. A batch biodegradability test was conducted with selected ortho-substituted alkylphenols (2-cresol, 2,6-dimethylphenol and 2-ethylphenol), fuel oxygenates (methyl tert-butyl ether, ethyl tert-butyl ether and tert-amylmethyl ether) and tert-butyl
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
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
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
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