H3766
Sodium 4-hydroxybenzoate
analytical standard
Synonym(s):
Sodium p-hydroxybenzoate, 4-Hydroxybenzoic acid sodium salt
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About This Item
Linear Formula:
4-HOC6H4CO2Na
CAS Number:
Molecular Weight:
160.10
Beilstein:
4163553
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24
grade
analytical standard
Quality Level
Assay
≥98.0% (HPLC)
technique(s)
HPLC: suitable
gas chromatography (GC): suitable
application(s)
food and beverages
format
neat
SMILES string
[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
InChI key
ZLVSYODPTJZFMK-UHFFFAOYSA-M
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Application
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).
Other Notes
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.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 2
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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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