Not soluble in water. Soluble in alcohol and dichloro ethane
55540
4-(Hydroxymercuri)benzoic acid sodium salt
≥95.0% (Hg)
Synonym(s):
p-Chloromercuribenzoate, p-Hydroxymercuribenzoic acid sodium salt, PCMB, Sodium 4-(hydroxymercurio)benzoate
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5 G
HUF 42,100.00
25 G
HUF 169,000.00
About This Item
Empirical Formula (Hill Notation):
C7H5HgNaO3
CAS Number:
Molecular Weight:
360.69
UNSPSC Code:
12352103
NACRES:
NA.25
PubChem Substance ID:
EC Number:
205-340-5
Beilstein/REAXYS Number:
6118796
MDL number:
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Product Name
4-(Hydroxymercuri)benzoic acid sodium salt, ≥95.0% (Hg)
InChI key
CBELQCYFTSHKPJ-UHFFFAOYSA-L
InChI
1S/C7H5O2.Hg.Na.H2O/c8-7(9)6-4-2-1-3-5-6;;;/h2-5H,(H,8,9);;;1H2/q;2*+1;/p-2
SMILES string
[Na+].O[Hg]c1ccc(cc1)C([O-])=O
assay
≥95.0% (Hg)
mp
≥300 °C
Quality Level
Looking for similar products? Visit Product Comparison Guide
1 of 4
This Item | 455652 | 89720 | H3766 |
|---|---|---|---|
| assay ≥95.0% (Hg) | assay 95% | assay ≥96.0% (NT) | assay ≥98.0% (HPLC) |
| Quality Level 100 | Quality Level 200 | Quality Level 200 | Quality Level 100 |
| mp ≥300 °C | mp >300 °C (lit.) | mp - | mp - |
Application
4-(Hydroxymercuri)benzoic acid is an organic mercurial compound that reacts via mercury-sulfur affinity with sulfhydryl groups in peptides, proteins and other molecules. PCMB may be used for the determination of sulfhydryl groups in proteins according to Boyer[1], by atomic absorption[2], and stopped-flow measurements, G. Castronuovo-Lepore et al.[3]. It may be used for specific applications such as probing the active site of an enzyme such as cytochrome C oxidase. 4-(Hydroxymercuri)benzoic acid appeared mistakenly as p-chloromercuriobenzoate [PCMB] in earlier literature.
Disclaimer
For U.S. Customers: Contains mercury; Do not place in trash - dispose according to local, state, or federal laws.
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Danger
Hazard Classifications
Acute Tox. 1 Dermal - Acute Tox. 2 Inhalation - Acute Tox. 2 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - STOT RE 2
Storage Class
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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Jörg R Aschenbach et al.
American journal of physiology. Gastrointestinal and liver physiology, 296(5), G1098-G1107 (2009-03-07)
The present study investigated the significance of apical transport proteins for ruminal acetate absorption and their interaction with different anions. In anion competition experiments in the washed reticulorumen, chloride disappearance rate (initial concentration, 28 mM) was inhibited by the presence
Determination of protein thiol groups by atomic absorption spectrometry.
M Suzuki et al.
Analytical biochemistry, 32(1), 106-117 (1969-10-15)
Yulan Rao et al.
Journal of agricultural and food chemistry, 58(3), 1462-1468 (2010-01-13)
A liquid chromatography method with mass spectrometric detection has been developed for the simultaneous determination of six thiols in the sulfur metabolic pathway, including cysteine (Cys), homocysteine (HCys), glutathione (GSH), cysteinyl-glycine (Cys-Gly), gamma-glutamyl-cysteine (Glu-Cys), and S-adenosyl-homocysteine (AdoHcy). Tris(2-carboxyethyl)phosphine (TCEP) was
Cristian Follmer et al.
European journal of biochemistry, 271(7), 1357-1363 (2004-03-20)
In this work we compared two plant ureases, jackbean urease (JBU) and embryo-specific soybean urease (SBU) and a bacterial (Bacillus pasteurii) urease, for kinetic parameters and other biological properties described recently for ureases that are independent of the ureolytic activity.
Nadia Farhat et al.
Water research, 142, 227-235 (2018-06-11)
The bacterial growth potential is important to understand and manage bacterial regrowth-related water quality concerns. Bacterial growth potential depends on growth promoting/limiting compounds, therefore, nutrient availability is the key factor governing bacterial growth potential. Selecting proper tools for bacterial growth
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