H3766
Sodium 4-hydroxybenzoate
analytical standard
Sinônimo(s):
Sodium p-hydroxybenzoate, 4-Hydroxybenzoic acid sodium salt
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About This Item
Fórmula linear:
4-HOC6H4CO2Na
Número CAS:
Peso molecular:
160.10
Beilstein:
4163553
Número CE:
Número MDL:
Código UNSPSC:
41116107
ID de substância PubChem:
NACRES:
NA.24
Produtos recomendados
grau
analytical standard
Nível de qualidade
Ensaio
≥98.0% (HPLC)
técnica(s)
HPLC: suitable
gas chromatography (GC): suitable
aplicação(ões)
food and beverages
formato
neat
cadeia de caracteres SMILES
[Na+].Oc1ccc(cc1)C([O-])=O
InChI
1S/C7H6O3.Na/c8-6-3-1-5(2-4-6)7(9)10;/h1-4,8H,(H,9,10);/q;+1/p-1
chave InChI
ZLVSYODPTJZFMK-UHFFFAOYSA-M
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Aplicação
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Sodium 4-hydroxybenzoate has been used to study its catalytic esterification with benzyl bromide by ultrasound-assisted solid–liquid phase-transfer catalysis (U-SLPTC) using the novel dual-site phase-transfer catalyst 4,40-bis(tributylammoniomethyl)-1,10-biphenyl dichloride (BTBAMBC).
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Palavra indicadora
Warning
Frases de perigo
Declarações de precaução
Classificações de perigo
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Órgãos-alvo
Respiratory system
Código de classe de armazenamento
11 - Combustible Solids
Classe de risco de água (WGK)
WGK 2
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
Equipamento de proteção individual
dust mask type N95 (US), Eyeshields, Gloves
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Journal of industrial microbiology & biotechnology, 46(1), 91-99 (2018-11-06)
Since the 1930s, parabens have been employed widely as preservatives in food, pharmaceutical, and personal care products. These alkyl esters of benzoic acid occur naturally in a broad range of plant species, where they are thought to enhance overall fitness
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
Jian-Shuang Jiang et al.
Journal of Asian natural products research, 15(5), 427-432 (2013-04-23)
Two new glycoside compounds, named saffloquinoside C (1) and (-)-4-hydroxybenzoic acid-4-O-[6'-O-(2″-methylbutyryl)-β-D-glucopyranoside] (2), were isolated from the florets of Carthamus tinctorius. Their structures were elucidated by detailed spectroscopic means including UV, IR, HR-ESI-MS, 1D and 2D NMR, and CD data. Compound
Clive S Barker et al.
PloS one, 7(8), e44030-e44030 (2012-09-07)
The bacterial type III export apparatus is found in the flagellum and in the needle complex of some pathogenic Gram-negative bacteria. In the needle complex its function is to secrete effector proteins for infection into Eukaryotic cells. In the bacterial
Danni Huang et al.
Journal of separation science, 35(13), 1667-1674 (2012-07-05)
In this work, magnetic multiwalled carbon nanotubes were synthesized through a facile hydrothermal process, and then successfully used as magnetic solid-phase extraction sorbents for the determination of p-hydroxybenzoates in beverage. The prepared magnetic multiwalled carbon nanotubes presented both satisfactory superparamagnetism
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