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线性分子式:
HOC6H4CO2CH2C6H5
化学文摘社编号:
分子量:
228.24
UNSPSC Code:
12352100
NACRES:
NA.24
PubChem Substance ID:
EC Number:
202-311-9
Beilstein/REAXYS Number:
2115995
MDL number:
InChI key
MOZDKDIOPSPTBH-UHFFFAOYSA-N
InChI
1S/C14H12O3/c15-13-8-6-12(7-9-13)14(16)17-10-11-4-2-1-3-5-11/h1-9,15H,10H2
SMILES string
Oc1ccc(cc1)C(=O)OCc2ccccc2
grade
analytical standard
assay
≥98.0% (GC)
shelf life
limited shelf life, expiry date on the label
Quality Level
application(s)
environmental
format
neat
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General description
Benzyl 4-hydroxybenzoate is an ester of para-hydroxy benzoic acid. It is used as a preservative, colorless dye and color developing agent in cosmetics and personal care products.
Application
Benzyl 4-hydroxybenzoate may be used as an analytical standard for the determination of the analyte in cosmetics, personal care products and pharmaceutical formulations by chromatography and spectrometry techniques.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Determination of parabens in pharmaceutical formulations by solid-phase microextraction-ion mobility spectrometry
Lokhnauth JK and Snow NH
Analytical Chemistry, 77(18), 5938-5946 (2005)
Determination of Preservatives in Cosmetics and Personal Care Products by LC-MS-MS
Myers EA, et al.
LCGC North America, 33, 16-22 (2015)
Validation of HPLC analysis of 2-phenoxyethanol, 1-phenoxypropan-2-ol, methyl, ethyl, propyl, butyl and benzyl 4-hydroxybenzoate (parabens) in cosmetic products, with emphasis on decision limit and detection capability.
Borremans M, et al.
Chromatographia, 59(1-2), 47-53 (2004)
Hung-Ming Yang et al.
Ultrasonics sonochemistry, 21(1), 395-400 (2013-08-27)
The catalytic esterification of sodium 4-hydroxybenzoate with benzyl bromide by ultrasound-assisted solid-liquid phase-transfer catalysis (U-SLPTC) was investigated using the novel dual-site phase-transfer catalyst 4,4'-bis(tributylammoniomethyl)-1,1'-biphenyl dichloride (BTBAMBC), which was synthesized from the reaction of 4,4'-bis(chloromethyl)-1,1'-biphenyl and tributylamine. Without catalyst and in
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