所有图片(1)
About This Item
线性分子式:
(CH3)2C6H3OH
CAS号:
分子量:
122.16
Beilstein:
636244
EC 号:
MDL编号:
UNSPSC代码:
12164502
PubChem化学物质编号:
Flavis编号:
4.066
NACRES:
NA.21
性状检查:
burnt; roasted
等级:
Fragrance grade
Halal
Halal
生物来源:
synthetic
Agency:
follows IFRA guidelines
食品过敏原:
no known allergens
推荐产品
生物来源
synthetic
质量水平
等级
Fragrance grade
Halal
Agency
follows IFRA guidelines
管理合规性
EU Regulation 1223/2009
蒸汽压
0.1 mmHg ( 25 °C)
方案
≥98%
折射率
n20/D 1.538 (lit.)
沸点
211-212 °C (lit.)
mp
22-23 °C (lit.)
密度
1.011 g/mL at 25 °C (lit.)
应用
flavors and fragrances
文件
see Safety & Documentation for available documents
食品过敏原
no known allergens
致敏芳香化合物
no known allergens
性状检查
burnt; roasted
SMILES字符串
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
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警示用语：
Danger
危险分类
Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Aquatic Chronic 2 - Eye Dam. 1 - Skin Corr. 1B - Skin Sens. 1B
储存分类代码
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
WGK
WGK 3
闪点(°F)
201.2 °F - closed cup
闪点(°C)
94.0 °C - closed cup
个人防护装备
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
法规信息
危险化学品
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)
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
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
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
B Bukowska et al.
Blood cells, molecules & diseases, 39(3), 238-244 (2007-07-27)
The effect of phenolic compounds: phenol, 2,4-dichlorophenol (2,4-DCP), 2,4-dimethylphenol (2,4-DMP) and catechol on human erythrocytes was studied. The level of fluorescent label - 6-carboxy-2',7'-dichlorodihydrofluorescein diacetate (H(2)DCFDA) oxidation by phenolic compounds in erythrocytes as well as the carbonyl group content and
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