Tetramethylammoniumbisulfate hydrate - for ion pair chromatography, ≥99%(T) , CAS No.80526-82-5

CAS: 80526-82-5 Cat. No.: T102977 Formule: C₄H₁₃NO₄S Poids moléculaire: 171.22 Beilstein Registry Number: 4829202 Numéro CE: 279-490-5 PubChem CID: 157340

GRADE & PURITY for Ion pair chromatography, ≥99%(T)

Synonyms

EINECS 279-490-5 | AMY13717 | AC7796 | D95778 | DTXSID10230376 | hydrogen sulfate; tetramethylammonium | MFCD00036149 | AKOS015915112 | SY037155 | Tetramethyl ammonium hydrogen sulphate | Tetramethylammonium hydrogensulfate | tetramethylazanium hydrogen s

Storage

Room temperature

Shipped In

Normal

Vue d’ensemble

The application of ion-pairing reagents as mobile phase additives ensures the elution of ionic and highly polar substances on reversed phase HPLC columns. The purity of mobile phase additives is of foremost significance for their successful utilization. 

Specifications

Synonymes

EINECS 279-490-5 | AMY13717 | AC7796 | D95778 | DTXSID10230376 | hydrogen sulfate; tetramethylammonium | MFCD00036149 | AKOS015915112 | SY037155 | Tetramethyl ammonium hydrogen sulphate | Tetramethylammonium hydrogensulfate | tetramethylazanium hydrogen s

Spécifications et pureté

for ion pair chromatography, ≥99%(T)

Conditions de stockage de stockage

Room temperature

Expédié en

Normal

Grade

pour la chromatographie par paires d'ions

Pureté

≥99%(T)

Noms et identifiants

• Pubchem Sid: 488188274
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488188274
• Sourires canoniques: C[N+](C)(C)C.OS(=O)(=O)[O-]
• IUPAC Name: hydrogen sulfate;tetramethylazanium
• InChIKey: DWTYPCUOWWOADE-UHFFFAOYSA-M
• INCHI: 1S/C4H12N.H2O4S/c2*1-5(2,3)4/h1-4H3;(H2,1,2,3,4)/q+1;/p-1
• Isomères SMILES: C[N+](C)(C)C.OS(=O)(=O)[O-]
• WGK Allemagne: 3
• CAS alternatif: 103812-00-6
• PubChem CID: 157340
• Poids moléculaire: 171.22
• Beilstein: 4829202
• Reaxy-Rn: 4829202

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Classe Organic sulfuric acids and derivatives

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Classe: Organic sulfuric acids and derivatives
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Organic sulfuric acids and derivatives
• Alternative Parents: Tetraalkylammonium salts Organopnictogen compounds Organic salts Organic oxides Hydrocarbon derivatives Amines
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Tetraalkylammonium salt - Quaternary ammonium salt - Organic sulfuric acid or derivatives - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organic salt - Organonitrogen compound - Amine - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as organic sulfuric acids and derivatives. These are organic compounds containing the sulfuric acid or a derivative thereof.
• 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

Propriétés chimiques et physiques

• Solubilité: Solubility in Water almost transparency
• Poids moléculaire: 171.220 g/mol
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 0
• Exact Mass: 171.057 Da
• Monoisotopic Mass: 171.057 Da
• Topological Polar Surface Area: 85.800 Ų
• Heavy Atom Count: 10
• Formal Charge: 0
• Complexity: 95.100
• 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: 2

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