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线性分子式:
(CH3)2C6H3OH
化学文摘社编号:
分子量:
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
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
signalword
Danger
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Aquatic Chronic 2 - Eye Dam. 1 - Skin Corr. 1B - Skin Sens. 1B
存储类别
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
法规信息
危险化学品
此项目有
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
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
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
J P Ghosh et al.
Chemosphere, 71(9), 1709-1717 (2008-02-13)
The potential use of laccase (SP-504) in an advanced oxidation-based treatment technology to remove 2,4-dimethylphenol (DMP) from water was investigated with and without the additive, polyethylene glycol (PEG). The DMP concentration was varied between 1.0 and 5.0 mM. The optimization
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