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W324906

Sigma-Aldrich

2,6-Xylenol

≥99%, FG

Sinonimo/i:

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

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About This Item

Formula condensata:
(CH3)2C6H3OH
Numero CAS:
576-26-1
Peso molecolare:
122.16
Numero FEMA:
3249
Beilstein:
1446677
Numero CE:
209-400-1
N° CoE:
11261
Numero MDL:
MFCD00002240
Codice UNSPSC:
12164502
ID PubChem:
24901585
Numero Flavis:
4.042
NACRES:
NA.21
Organolettico:
medicinal
Grado:
FG
Fragrance grade
Halal
Origine biologica:
synthetic
agenzia:
follows IFRA guidelines
meets purity specifications of JECFA
Allergene alimentare:
no known allergens

Origine biologica

synthetic

Livello qualitativo

400

Grado

FG
Fragrance grade
Halal

agenzia

follows IFRA guidelines
meets purity specifications of JECFA

Conformità normativa

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

Saggio

≥99%

Temp. autoaccensione

1110 °F

P. ebollizione

203 °C (lit.)

Punto di fusione

43-45 °C (lit.)

applicazioni

flavors and fragrances

Documentazione

see Safety & Documentation for available documents

Allergene alimentare

no known allergens

Allergene in fragranze

no known allergens

Organolettico

medicinal

Stringa SMILE

Cc1cccc(C)c1O

InChI

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

Informazioni sul gene

human ... GABRA1(2554)

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Applicazioni


  • 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).

Avvertenze

Danger

Indicazioni di pericolo

H301 + H311,H314,H335,H411

Classi di pericolo

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

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

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

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

186.8 °F - closed cup

Punto d’infiammabilità (°C)

86 °C - closed cup

Dispositivi di protezione individuale

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

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Certificati d'analisi (COA)

Lot/Batch Number
STBK0173
STBJ7900
STBJ6700
STBJ0714
STBH8789

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Eparina

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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