230626
4-丁基苯甲酸
99%
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关于此项目
线性分子式:
CH3(CH2)3C6H4CO2H
化学文摘社编号:
分子量:
178.23
EC Number:
243-940-9
UNSPSC Code:
12352103
PubChem Substance ID:
Beilstein/REAXYS Number:
2044046
MDL number:
产品名称
4-丁基苯甲酸, 99%
InChI key
JFKUBRAOUZEZSL-UHFFFAOYSA-N
InChI
1S/C11H14O2/c1-2-3-4-9-5-7-10(8-6-9)11(12)13/h5-8H,2-4H2,1H3,(H,12,13)
SMILES string
CCCCc1ccc(cc1)C(O)=O
assay
99%
form
liquid crystal
mp
100-113 °C (lit.)
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存储类别
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
此项目有
Mette Kristensen et al.
Journal of chromatography. A, 1601, 21-26 (2019-05-13)
Gas-chromatography (GC) analysis of carboxylic acids is limited by the high polarity and low volatility of most of these compounds. Boron trifluoride (BF3) mediated alkylation reactions is one of the most commonly used derivatization methods for making carboxylic acids GC
Dieter Schemeth et al.
Analytica chimica acta, 1038, 182-190 (2018-10-04)
In this study, we focus on isolation and fractionation strategies by solid phase extraction (SPE) for a broad range of environmentally related organic acids. These emerging potential contaminants are primary degradation products of spilled petrogenic compounds but little attention has
Chao-Bin Xue et al.
Bioorganic & medicinal chemistry, 15(5), 2006-2015 (2007-01-30)
Phenoloxidase (PO), also known as tyrosinase, is a key enzyme in insect development, responsible for catalyzing the hydroxylation of tyrosine into o-diphenols and the oxidation of o-diphenols into o-quinones. Inhibition of PO may provide a basis for novel environmentally friendly
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