Adenine hemisulfate salt - for cell culture, ≥98% , CAS No.321-30-2

CAS: 321-30-2 Cat. No.: A112852 Molecular Weight: 368.34 Beilstein Registry Number: 3820263 EC Number: 206-286-5 PubChem CID: 9449

GRADE & PURITY for Cell culture, ≥98%

Synonyms

Adenine hemisulfate salt, powder, BioReagent, suitable for cell culture | Adenine, sulfate (2:1) | 7H-Purin-6-amine hemisulfate | 1h-purin-6-amine sulfate(2:1) | Adenine hemisulfate salt | ADENINE SULFATE | Adenine sulfate (2:1) | 1H-Purin-6-amine, sulfat

Storage

Room temperature

Shipped In

Normal

Specifications

Synonyms

Adenine hemisulfate salt, powder, BioReagent, suitable for cell culture | Adenine, sulfate (2:1) | 7H-Purin-6-amine hemisulfate | 1h-purin-6-amine sulfate(2:1) | Adenine hemisulfate salt | ADENINE SULFATE | Adenine sulfate (2:1) | 1H-Purin-6-amine, sulfat

Specifications & Purity

for cell culture, ≥98%

Storage

Room temperature

Shipped In

Normal

Grade

for Cell culture

Purity

≥98%

Names and Identifiers

• Pubchem Sid: 488180981
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488180981
• Canonical Smiles: C1=NC2=NC=NC(=C2N1)N.C1=NC2=NC=NC(=C2N1)N.OS(=O)(=O)O
• IUPAC Name: 7H-purin-6-amine;sulfuric acid
• InChIKey: LQXHSCOPYJCOMD-UHFFFAOYSA-N
• INCHI: 1S/2C5H5N5.H2O4S/c2*6-4-3-5(9-1-7-3)10-2-8-4;1-5(2,3)4/h2*1-2H,(H3,6,7,8,9,10);(H2,1,2,3,4)
• Isomeric SMILES: C1=NC2=NC=NC(=C2N1)N.C1=NC2=NC=NC(=C2N1)N.OS(=O)(=O)O
• WGK Germany: 3
• RTECS: AU7140000
• Alternate CAS: 6509-19-9
• PubChem CID: 9449
• UN Number: 2811
• Packing Group: III
• Molecular Weight: 368.34
• Beilstein: 3820263

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Class Imidazopyrimidines
      • Subclass Purines and purine derivatives

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Class: Imidazopyrimidines
• Subclass: Purines and purine derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: 6-aminopurines
• Alternative Parents: Aminopyrimidines and derivatives Organic sulfuric acids Imidolactams Imidazoles Heteroaromatic compounds Azacyclic compounds Primary amines Organopnictogen compounds Organic oxides Hydrocarbon derivatives
• Molecular Framework: Not available
• Substituents: 6-aminopurine - Aminopyrimidine - Sulfuric acid - Pyrimidine - Imidolactam - Azole - Imidazole - Organic sulfuric acid or derivatives - Heteroaromatic compound - Azacycle - Primary amine - Organonitrogen compound - Organic oxygen compound - Organopnictogen compound - Amine - Organic nitrogen compound - Organic oxide - Hydrocarbon derivative - Aromatic heteropolycyclic compound
• Description: This compound belongs to the class of organic compounds known as 6-aminopurines. These are purines that carry an amino group at position 6. Purine is a bicyclic aromatic compound made up of a pyrimidine ring fused to an imidazole ring.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Chemical and Physical Properties

• Solubility: Soluble in water (4 mg/ml), ethanol (<1 mg/ml at 25°C), DMSO (<1 mg/ml at 25°C), and HCl (10 mg/ml).
• Sensitivity: Hygroscopic
• Melt Point(°C): 205 °C
• Molecular Weight: 368.340 g/mol
• Hydrogen Bond Donor Count: 6
• Hydrogen Bond Acceptor Count: 12
• Rotatable Bond Count: 0
• Exact Mass: 368.076 Da
• Monoisotopic Mass: 368.076 Da
• Topological Polar Surface Area: 244.000 Ų
• Heavy Atom Count: 25
• Formal Charge: 0
• Complexity: 209.000
• 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: 3

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