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W359602

Sigma-Aldrich

3,4-Dimethylphenol

≥98%, FG

Sinónimos:

3,4-Dimethylphenol, 4-Hydroxy-o-xylene

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About This Item

Fórmula lineal:
(CH3)2C6H3OH
Número de CAS:
95-65-8
Peso molecular:
122.16
Número de FEMA:
3596
Beilstein:
1099267
Número CE:
202-439-5
nº del Consejo Europeo:
11262
Número MDL:
MFCD00002304
Código UNSPSC:
12164502
ID de la sustancia en PubChem:
24901802
Número Flavis:
4.048
NACRES:
NA.21
Organoléptico:
burnt
grado:
FG
Fragrance grade
Halal
origen biológico:
synthetic
Agency:
follows IFRA guidelines
meets purity specifications of JECFA
alérgeno alimentario:
no known allergens

origen biológico

synthetic

Nivel de calidad

400

grado

FG
Fragrance grade
Halal

Agency

follows IFRA guidelines
meets purity specifications of JECFA

cumplimiento norm.

EU Regulation 1223/2009
EU Regulation 1334/2008 & 872/2012

Ensayo

≥98%

bp

227 °C (lit.)

aplicaciones

flavors and fragrances

Documentación

see Safety & Documentation for available documents

alérgeno alimentario

no known allergens

alérgeno de la fragancia

no known allergens

Organoléptico

burnt

cadena SMILES

Cc1ccc(O)cc1C

InChI

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

Clave InChI

YCOXTKKNXUZSKD-UHFFFAOYSA-N

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Aplicación


  • Green Aromatic Epoxidation with an Iron Porphyrin Catalyst for One-Pot Functionalization of Renewable Xylene, Quinoline, and Acridine.: This study explores the green epoxidation of aromatic compounds using an iron porphyrin catalyst, demonstrating effective one-pot functionalization of renewable xylene derivatives, including 3,4-xylenol (Corrêa et al., 2023).

  • A highly expressed odorant receptor from the yellow fever mosquito, AaegOR11, responds to (+)- and (-)-fenchone and a phenolic repellent.: This research identifies an odorant receptor in mosquitoes that responds to various compounds, including 3,4-dimethylphenol, which could have implications for developing new repellents (Lu et al., 2022).


Palabra de señalización

Danger

Frases de peligro

H301 + H311,H314,H411

Clasificaciones de peligro

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

Código de clase de almacenamiento

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

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

230.0 °F - closed cup

Punto de inflamabilidad (°C)

110 °C - closed cup

Equipo de protección personal

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

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Certificados de análisis (COA)

Lot/Batch Number
SHBR9311
SHBR4849
SHBQ5318
SHBR2413
SHBQ1420

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Sigma-Aldrich

W274615

Dimetilsulfuro

A P Hart et al.
Journal of forensic sciences, 42(4), 693-696 (1997-07-01)
Phenol (carbolic acid) is widely used as a disinfectant as well as in the chemical industry as an intermediate in the synthesis of a variety of chemicals. Phenol is also the major metabolite of benzene which is used in many
Maria Concetta Tomei et al.
Environmental science and pollution research international, 15(3), 188-195 (2008-05-28)
In this study, attention was focused on substituted phenols because of their widespread presence in industrial effluents originating from many different sources: they are major constituents of wastewater from coal conversion processes, coke ovens, petroleum refineries and petrochemical industries, resin
M Bartilson et al.
Molecular & general genetics : MGG, 220(2), 294-300 (1990-01-01)
The gene organization of the phenol catabolic pathway of Pseudomonas CF600 has been investigated. This strain can grow on phenol and some methylated phenols by virtue of an inducible phenol hydroxylase and metacleavage pathway enzymes. The genes coding for these
A Dasgupta et al.
Journal of forensic sciences, 42(4), 697-700 (1997-07-01)
Benzyl alcohol is commonly used as an antibacterial agent in a variety of pharmaceutical formulations. Several fatalities in neonates have been linked to benzyl alcohol poisoning. Most methods for measuring benzyl alcohol concentrations in serum utilize direct extraction followed by
V Shingler et al.
Journal of bacteriology, 174(3), 711-724 (1992-02-01)
The meta-cleavage pathway for catechol is one of the major routes for the microbial degradation of aromatic compounds. Pseudomonas sp. strain CF600 grows efficiently on phenol, cresols, and 3,4-dimethylphenol via a plasmid-encoded multicomponent phenol hydroxylase and a subsequent meta-cleavage pathway.
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