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p-Aminophenylmercuric acetate - 0.93, high purity , CAS No.6283-24-5

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Item Number
P649286
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SKU Size
Availability
Price Qty
P649286-10mg
10mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$36.90
P649286-50mg
50mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$110.90
P649286-100mg
100mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$199.90

Basic Description

Synonyms p-Aminophenylmercuric Acetate - CAS 6283-24-5 - Calbiochem | Mercury, (acetato-O)(4-aminophenyl)- | Mercury, (acetato-.kappa.O)(4-aminophenyl)- | acetoxymercurianiline | FT-0617597 | 4-Aminophenylmercury acetate | 1,3-Bis(2,4-diaminophenoxy)propane 4HCl,
Specifications & Purity Moligand™, ≥98%
Biochemical and Physiological Mechanisms p-Aminophenylmercuric acetate is an organomercurial activator of matrix metalloproteinases (MMP) . P-Aminophenylmercuric acetate participates in the activation and inhibition of MMP-8 by attacking protein sulfhydryl or inducing cysteine switching reaction
Storage Temp Store at -20°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Grade Moligand™
Product Description

p-Aminophenylmercuric acetate is an organomercurial activator of matrix metalloproteinases (MMP). P-Aminophenylmercuric acetate participates in the activation and inhibition of MMP-8 by attacking protein sulfhydryl or inducing cysteine switching reaction. p-Aminophenylmercuric acetate promotes the shedding of betacellulin precursor (pro-BTC). p-Aminophenylmercuric acetate influences the binding of agonists and antagonists to the opiate receptor .

In Vitro

p-Aminophenylmercuric acetate (APMA) (0-30 µM; 20 min) decreases the apparent number of dihydromorphine binding sites and increases the sensitivity of agonist binding to the inhibitory effects of sodium in rat brain homogenate. p-Aminophenylmercuric acetate (0.5 mM; 30 min) activates the MMP-2 and MMP-9. MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Form:Solid

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Benzenoids
Class Benzene and substituted derivatives
Subclass Aniline and substituted anilines
Intermediate Tree Nodes Not available
Direct Parent Aniline and substituted anilines
Alternative Parents Metal aryls  Aryl mercury compounds  Organic transition metal salts  Monocarboxylic acids and derivatives  Carboxylic acids  Primary amines  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  Organic cations  
Molecular Framework Not available
Substituents Aniline or substituted anilines - Aryl mercury compound - Metal aryl - Carboxylic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Organic transition metal salt - Organic nitrogen compound - Primary amine - Organooxygen compound - Organonitrogen compound - Organometallic compound - Organomercurial-compound - Organic transition metal moeity - Carbonyl group - Amine - Organic oxygen compound - Hydrocarbon derivative - Organic oxide - Organic cation - Aromatic homomonocyclic compound
Description This compound belongs to the class of organic compounds known as aniline and substituted anilines. These are organic compounds containing an aminobenzene moiety.
External Descriptors Not available

Names and Identifiers

IUPAC Name acetyloxy-(4-aminophenyl)mercury
INCHI InChI=1S/C6H6N.C2H4O2.Hg/c7-6-4-2-1-3-5-6;1-2(3)4;/h2-5H,7H2;1H3,(H,3,4);/q;;+1/p-1
InChIKey RXSUFCOOZSGWSW-UHFFFAOYSA-M
Smiles CC(=O)O[Hg]C1=CC=C(C=C1)N
Isomeric SMILES CC(=O)O[Hg]C1=CC=C(C=C1)N
Molecular Weight 351.75

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

9 results found

Lot Number Certificate Type Date Item
F2509508 Certificate of Analysis May 29, 2025 P649286
F2509510 Certificate of Analysis May 29, 2025 P649286
F2509525 Certificate of Analysis May 29, 2025 P649286
F2509509 Certificate of Analysis May 29, 2025 P649286
K2411330 Certificate of Analysis Nov 05, 2024 P649286
K2411331 Certificate of Analysis Nov 05, 2024 P649286
K2411332 Certificate of Analysis Nov 05, 2024 P649286
K2411333 Certificate of Analysis Nov 05, 2024 P649286
K2411334 Certificate of Analysis Nov 05, 2024 P649286

Chemical and Physical Properties

Solubility DMSO : 125 mg/mL (355.37 mM; ultrasonic and warming and heat to 60°C)
Molecular Weight 351.750 g/mol
XLogP3
Hydrogen Bond Donor Count 1
Hydrogen Bond Acceptor Count 3
Rotatable Bond Count 3
Exact Mass 353.034 Da
Monoisotopic Mass 353.034 Da
Topological Polar Surface Area 52.300 Ų
Heavy Atom Count 12
Formal Charge 0
Complexity 155.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 1

Citations of This Product

1. Feng Wu, Yu Huang, Xian Yang, Jing-Jing Hu, Xiaoding Lou, Fan Xia, Yanlin Song, Lei Jiang.  (2021)  Tunning Intermolecular Interaction of Peptide-Conjugated AIEgen in Nano-Confined Space for Quantitative Detection of Tumor Marker Secreted from Cells.  ANALYTICAL CHEMISTRY,  93  (48): (16257–16263). 
2. Zhu Dan, Zhong Hanyan, Shi Jingzhan, Liu Qiang, Wang Yiping.  (2025)  Ratiometric surface-enhanced Raman scattering quantification of extracellular matrix metalloproteinase-2 activity for tumor diagnosis.  ANALYTICAL AND BIOANALYTICAL CHEMISTRY,    (1-11). 

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