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Merck
CN

W506206

2,4-Xylenol

≥98%

Synonym(s):

2,4-Dimethylphenol, 4-Hydroxy-m-xylene, asym.-m-Xylenol

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About This Item

Linear Formula:
(CH3)2C6H3OH
CAS Number:
Molecular Weight:
122.16
NACRES:
NA.21
Flavis number:
4.066
PubChem Substance ID:
UNSPSC Code:
12164502
EC Number:
203-321-6
MDL number:
Beilstein/REAXYS Number:
636244
Organoleptic:
burnt; roasted
Grade:
Fragrance grade, Halal
Biological source:
synthetic
Agency:
follows IFRA guidelines
Food allergen:
no known allergens
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biological source

synthetic

Quality Level

grade

Fragrance grade, Halal

agency

follows IFRA guidelines

reg. compliance

EU Regulation 1223/2009

vapor pressure

0.1 mmHg ( 25 °C)

assay

≥98%

refractive index

n20/D 1.538 (lit.)

bp

211-212 °C (lit.)

mp

22-23 °C (lit.)

density

1.011 g/mL at 25 °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

burnt; roasted

SMILES string

Cc1ccc(O)c(C)c1

InChI

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

InChI key

KUFFULVDNCHOFZ-UHFFFAOYSA-N

signalword

Danger

Hazard Classifications

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

Storage Class

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

wgk

WGK 3

flash_point_f

201.2 °F - closed cup

flash_point_c

94.0 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

Regulatory Information

危险化学品

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B Bukowska et al.
Biochemistry and molecular biology international, 45(1), 47-59 (1998-06-23)
The effect of phenoxyherbicides and their metabolites on the structure of oxy- and deoxyhemoglobin was studied by using different doses and times of incubation of hemoglobin with the herbicide. It was ascertained that among the investigated hemoglobins the most sensitive
Peipei Qi et al.
Talanta, 81(4-5), 1630-1635 (2010-05-06)
A molecularly imprinted polymer (MIP) was prepared using 2,4-dimethylphenol (2,4-DMP) as template. The synthesis is optimized by using three different porogens, chloroform, acetonitrile and toluene. The MIP was used as a class-selective sorbent in molecularly imprinted solid-phase extraction (MIP-SPE) for
Metabolism and distribution of 2,4-dimethylphenol in rat.
J S Kaka et al.
Ecotoxicology and environmental safety, 6(1), 35-40 (1982-02-01)
C C Agee et al.
Antimicrobial agents and chemotherapy, 18(2), 243-248 (1980-08-01)
Mycoplasma pneumoniae induces pneumonia-like symptoms in hamsters and causes ciliostasis and cytonecrosis in hamster tracheal explants. 2,4-Dimethylphenol and, to a lesser extent, its 2,3-, 2,5-, and 2,6-dimethylphenol isomers protected tracheal explants from these changes after exposure to virulent M. pneumoniae
Diversity-oriented synthesis of polycyclic scaffolds by modification of an anodic product derived from 2,4-dimethylphenol.
Joaquin Barjau et al.
Angewandte Chemie (International ed. in English), 50(6), 1415-1419 (2011-02-04)

Related Content

Global Trade Item Number

SKUGTIN
W506206-1KG04061837847011
W506206-SAMPLE04061837847028

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