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H3766

Supelco

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

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).

Produtos recomendados

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Pictogramas

Exclamation mark

Palavra indicadora

Warning

Frases de perigo

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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Certificados de análise (COA)

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Sigma-Aldrich

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Jillian M Hagel et al.
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
Ruth Pietri et al.
The Journal of biological chemistry, 287(28), 23748-23756 (2012-05-12)
Rhodopseudomonas palustris metabolizes aromatic compounds derived from lignin degradation products and has the potential for bioremediation of xenobiotic compounds. We recently identified four possible solute-binding proteins in R. palustris that demonstrated binding to aromatic lignin monomers. Characterization of these proteins
G Shanmugam et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 106, 175-184 (2013-02-06)
Large size and high quality single crystals of organic nonlinear optical material Piperidinium p-Hydroxybenzoate (PDPHB) have been grown by solution growth method. This crystal belongs to monoclinic system with a noncentrosymmetric space group of Cc. To confirm its structure and
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

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