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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:
105-67-9
Molecular Weight:
122.16
NACRES:
NA.21
Flavis number:
4.066
PubChem Substance ID:
24902027
UNSPSC Code:
12164502
EC Number:
203-321-6
MDL number:
MFCD00002233
Beilstein/REAXYS Number:
636244
Organoleptic:
burnt; roasted
Grade:
Fragrance grade, Halal
Biological source:
synthetic
Agency:
follows IFRA guidelines
Food allergen:
no known allergens

Key Documents

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InChI key

KUFFULVDNCHOFZ-UHFFFAOYSA-N

InChI

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

SMILES string

Cc1ccc(O)c(C)c1

biological source

synthetic

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

Quality Level

400

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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Certificates of Analysis (COA)

Lot/Batch Number
SHBN3638
SHBM5770
SHBL9339
MKCH1524
MKCG2930

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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)
F L Arenghi et al.
Applied and environmental microbiology, 67(7), 3304-3308 (2001-06-27)
Pseudomonas stutzeri OX1 meta pathway genes for toluene and o-xylene catabolism were analyzed, and loci encoding phenol hydroxylase, catechol 2,3-dioxygenase, 2-hydroxymuconate semialdehyde dehydrogenase, and 2-hydroxymuconate semialdehyde hydrolase were mapped. Phenol hydroxylase converted a broad range of substrates, as it was
Hiroko Tsukatani et al.
Analytica chimica acta, 682(1-2), 72-76 (2010-11-09)
Gas chromatography/supersonic jet/resonance-enhanced multiphoton ionization/time-of-flight mass spectrometry (GC/SSJ/REMPI/TOF-MS) was employed for isomer-selective determination of 2,4-xylenol in river and seawater samples. The sample containing 2,4-xylenol was measured using argon, rather than helium, as the GC carrier gas to cool the analyte
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
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