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4-Aminobenzoic acid sodium salt hydrate

Base Information
  • Chemical Name:4-Aminobenzoic acid sodium salt hydrate
  • CAS No.:206557-08-6
  • Molecular Formula:H2NC6H4CO2NaxH2O
  • Molecular Weight:159.12
  • Hs Code.:2922499990
  • ChEMBL ID:CHEMBL1437781
  • DSSTox Substance ID:DTXSID60583607
  • Mol file:206557-08-6.mol
4-Aminobenzoic acid sodium salt hydrate

Synonyms:4-Aminobenzoic acid sodium salt hydrate;206557-08-6;sodium;4-aminobenzoate;hydrate;4-AMINOBENZOIC ACID SODIUM SALT;MLS001335933;CHEMBL1437781;DTXSID60583607;HWVSNYIAZJHZFQ-UHFFFAOYSA-M;HMS2231H07;HMS3369E10;AKOS015888339;SMR000875340;Sodium 4-aminobenzoate--water (1/1/1);4-Aminobenzoic acid,sodium salt hydrate,99%;4-Aminobenzoic acid sodium salt hydrate, 99%

Suppliers and Price of 4-Aminobenzoic acid sodium salt hydrate
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • Sigma-Aldrich
  • 4-Aminobenzoic acid sodium salt hydrate 99%
  • 500g
  • $ 278.00
  • Sigma-Aldrich
  • 4-Aminobenzoic acid sodium salt hydrate 99%
  • 100g
  • $ 80.30
  • American Custom Chemicals Corporation
  • 4-AMINOBENZOIC ACID SODIUM SALT HYDRATE 95.00%
  • 500G
  • $ 4548.42
  • American Custom Chemicals Corporation
  • 4-AMINOBENZOIC ACID SODIUM SALT HYDRATE 95.00%
  • 100G
  • $ 2508.69
Total 3 raw suppliers
Chemical Property of 4-Aminobenzoic acid sodium salt hydrate
Chemical Property:
  • PSA:75.38000 
  • LogP:0.14920 
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:1
  • Exact Mass:177.04018740
  • Heavy Atom Count:12
  • Complexity:132
Purity/Quality:

96% *data from raw suppliers

4-Aminobenzoic acid sodium salt hydrate 99% *data from reagent suppliers

Safty Information:
  • Pictogram(s): Xi 
  • Hazard Codes:Xi 
  • Statements: 36/37/38 
  • Safety Statements: 26-36 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC(=CC=C1C(=O)[O-])N.O.[Na+]
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