Sodium 1-hexanesulfonate - ≥98% , CAS No.2832-45-3

CAS: 2832-45-3 Cat. No.: S104947 Molecular Weight: 188.22 Beilstein Registry Number: 3727014 EC Number: 220-601-3 PubChem CID: 23677630

GRADE & PURITY ≥98%

Synonyms

1-Hexanesulfonic acid, sodium salt (1:1) | AS-12243 | Sodium 1-Hexanesulfonate | I0344 | F10020 | J-524256 | EINECS 220-601-3 | AI3-18426C | 1-HEXANE SULFONIC ACID SALT, ANHYD salt | H0447 | Sodium hexane-1-sulphonate | SY001279 | AKOS006222992 | EN300-64

Storage

Argon charged,Room temperature

Shipped In

Normal

Overview

Application：

Sodium 1-hexanesulfonate is used as a base in the organic coupling reactions such as Suzuki coupling reactions. It is used as an ion pairing reagent for HPLC and involved in the analysis of peptides and proteins. It is also used in high performance capillary electrophoresis analysis of peptides.

Specifications

Synonyms

1-Hexanesulfonic acid, sodium salt (1:1) | AS-12243 | Sodium 1-Hexanesulfonate | I0344 | F10020 | J-524256 | EINECS 220-601-3 | AI3-18426C | 1-HEXANE SULFONIC ACID SALT, ANHYD salt | H0447 | Sodium hexane-1-sulphonate | SY001279 | AKOS006222992 | EN300-64

Specifications & Purity

≥98%

Storage

Argon charged, Room temperature

Shipped In

Normal

Purity

≥98%

Names and Identifiers

• Pubchem Sid: 488200496
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488200496
• Canonical Smiles: CCCCCCS(=O)(=O)[O-].[Na+]
• IUPAC Name: sodium;hexane-1-sulfonate
• InChIKey: QWSZRRAAFHGKCH-UHFFFAOYSA-M
• INCHI: 1S/C6H14O3S.Na/c1-2-3-4-5-6-10(7,8)9;/h2-6H2,1H3,(H,7,8,9);/q;+1/p-1
• Isomeric SMILES: CCCCCCS(=O)(=O)[O-].[Na+]
• WGK Germany: 3
• PubChem CID: 23677630
• Molecular Weight: 188.22
• Beilstein: 3727014
• Reaxy-Rn: 3727014

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Class: 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
• Description: 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

Mechanisms of Action

Chemical and Physical Properties

• Solubility: Soluble in Water: 100 mg/ml
• Sensitivity: Moisture sensitive.
• Melt Point(°C): 300°C
• Molecular Weight: 188.220 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 5
• Exact Mass: 188.048 Da
• Monoisotopic Mass: 188.048 Da
• Topological Polar Surface Area: 65.600 Ų
• Heavy Atom Count: 11
• Formal Charge: 0
• Complexity: 159.000
• 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: 2

XLogP3

References

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