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About This Item
Linear Formula:
CH3(CH2)3C6H4CO2H
CAS Number:
Molecular Weight:
178.23
EC Number:
243-940-9
UNSPSC Code:
12352103
PubChem Substance ID:
Beilstein/REAXYS Number:
2044046
MDL number:
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.)
Storage Class
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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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)
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Chao-Bin Xue et al.
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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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