Sodium 1-heptanesulfonate monohydrate - for ion pair chromatography, ≥99% , CAS No.207300-90-1

CAS: 207300-90-1 Cat. No.: S189072 Peso molecular: 220.26 Número EC: 689-034-0 PubChem CID: 23687711

GRADE & PURITY for Ion pair chromatography, ≥99%

Synonyms

F10034 | Sodium 1-heptanesulfonate monohydrate | sodium;heptane-1-sulfonate;hydrate | Sodium 1-heptanesulfonate monohydrate, for HPLC, >=99% | Sodium1-heptanesulfonatemonohydrate | AKOS015909827 | SY011506 | 1-Heptanesulfonic acid sodium salt monohydrate

Storage

Room temperature

Shipped In

Normal

Descripción general

Sodium 1-heptanesulfonate monohydrate can be used as an ion-pairing (IP) reagent, to develop ion-pair reversed phase liquid chromatography method, for the determination of antituberculosis drug ethambutol hydrochloride.

Specifications

Sinónimos

F10034 | Sodium 1-heptanesulfonate monohydrate | sodium;heptane-1-sulfonate;hydrate | Sodium 1-heptanesulfonate monohydrate, for HPLC, >=99% | Sodium1-heptanesulfonatemonohydrate | AKOS015909827 | SY011506 | 1-Heptanesulfonic acid sodium salt monohydrate

Especificaciones y pureza

for ion pair chromatography, ≥99%

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Grado

for Ion pair chromatography

Pureza

≥99%

Nombres e identificadores

• Pubchem Sid: 488200538
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488200538
• Sonrisas canónicas: CCCCCCCS(=O)(=O)[O-].O.[Na+]
• IUPAC Name: sodium;heptane-1-sulfonate;hydrate
• InChIKey: XWZCREJRXRKIRQ-UHFFFAOYSA-M
• INCHI: 1S/C7H16O3S.Na.H2O/c1-2-3-4-5-6-7-11(8,9)10;;/h2-7H2,1H3,(H,8,9,10);;1H2/q;+1;/p-1
• Isómeros SMILES: CCCCCCCS(=O)(=O)[O-].O.[Na+]
• WGK Alemania: 3
• PubChem CID: 23687711
• Peso molecular: 220.26

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Clase Organic sulfonic acids and derivatives
      • Subclass Organosulfonic acids and derivatives

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Clase: Organic sulfonic acids and derivatives
• Subclass: Organosulfonic acids and derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Organosulfonic acids
• Alternative Parents: Sulfonyls Alkanesulfonic acids Organic sodium salts Organic oxides Hydrocarbon derivatives Organic cations
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Alkanesulfonic acid - Sulfonyl - Organosulfonic acid - Organic alkali metal salt - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organic sodium salt - Organic salt - Organosulfur compound - Organic cation - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as organosulfonic acids. These are compounds containing the sulfonic acid group, which has the general structure RS(=O)2OH (R is not a hydrogen atom).
• 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

Propiedades químicas y físicas

• Solubilidad: Slightly soluble in water.
• Punto de fusión (°C): >300°
• Peso molecular: 220.260 g/mol
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 6
• Exact Mass: 220.075 Da
• Monoisotopic Mass: 220.075 Da
• Topological Polar Surface Area: 66.600 Ų
• Heavy Atom Count: 13
• Formal Charge: 0
• Complexity: 172.000
• 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

XLogP3

Referencias

1. Hongfei Nie, Yarong Zhang, Haiyang Yu, Hong Xiao, Tao Li, Qian Yang.  (2021)  Oral delivery of carrier-free dual-drug nanocrystal self-assembled microspheres improved NAD+ bioavailability and attenuated cardiac ischemia/reperfusion injury in mice.  DRUG DELIVERY,      [PMID:33605178] [10.1080/10717544.2021.1886198]