138169
2,4-二甲基苯甲酸
98%
别名:
不对称间二甲苯酸
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关于此项目
线性分子式:
(CH3)2C6H3CO2H
化学文摘社编号:
分子量:
150.17
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
210-246-2
Beilstein/REAXYS Number:
971589
MDL number:
Assay:
98%
Form:
solid
产品名称
2,4-二甲基苯甲酸, 98%
InChI key
BKYWPNROPGQIFZ-UHFFFAOYSA-N
InChI
1S/C9H10O2/c1-6-3-4-8(9(10)11)7(2)5-6/h3-5H,1-2H3,(H,10,11)
SMILES string
Cc1ccc(c(C)c1)C(O)=O
assay
98%
form
solid
bp
267 °C/727 mmHg (lit.)
mp
124-126 °C (lit.)
functional group
carboxylic acid
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Application
2,4-二甲基苯甲酸用于 α-，β-，γ- 和 δ-环糊精的毛细管电泳分离。
General description
2,4-二甲基苯甲酸具有抗菌活性。它是假枯烯（1,2,4-三甲基苯）的代谢产物。
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
Capillary electrophoretic separation of α-, β-, γ-and δ-cyclodextrins using a dual electrolyte system.
Lambertsen KL and Zimmermann W.
Journal of Chromatography A, 811(1), 193-199 (1998)
J Cerf et al.
Archives of toxicology, 45(2), 93-100 (1980-07-01)
In order to identify biological indicators of exposure to trimethylbenzenes, the metabolism of pseudocumene (1,2,4-trimethylbenzene) was investigated in rabbits. After oral administration of this compound, urine was collected for several days and analyzed for the presence of acidic metabolites. Isolation
[Studies on antibacterial activities of secondary metabolites from fungus Cephalosporium sp. AL031].
Bi Yunmei et al.
Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials, 27(4), 270-272 (2004-08-17)
The antibacterial activity of fourteen identified compounds from secondary metabolites of fungus Cephalosporium sp. AL031 against eleven gram-positive or gram-negative bacteria in vitro was investigated by agar diffusion assay. The results suggested that two new compounds [S-(+)-5-hydroxymellein, S-(+)-7-hydroxymellein], together with
Radosław Swiercz et al.
International journal of occupational medicine and environmental health, 15(1), 37-42 (2002-06-01)
The objective of this study was to evaluate the toxicokinetics and metabolism of pseudocumene after inhalation exposure. Male Wistar rats were exposed to pseudocumene vapors at nominal concentrations of 25,100 or 250 ppm in the dynamic inhalation chambers for 6
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