Methanesulfonic acid - UltraPureChrom™, for HPLC, ≥99.5%(T) , CAS No.75-75-2

CAS: 75-75-2 Cat. No.: M433628 Summenformel: CH₄O₃S Molekulargewicht: 96.11 Beilstein Registry Number: 1446024 EG-Nummer: 200-898-6

GRADE & PURITY UltraPureChrom™, for HPLC, ≥99.5%(T)

Synonyms

12EH9M7279 | CHEBI:27376 | CCRIS 2783 | EINECS 200-898-6 | NSC 3718 | methansulfonic acid | HSDB 5004 | 03S | METHANESULFONIC ACID [MI] | STL264182 | Q414168 | ammoniummethanesulfonate | MSA | NCGC00258626-01 | CH3SO3H | DL-MALICACIDMONOSODIUMSALT | METHA

Storage

Room temperature

Shipped In

FedEx DG Service

Specifications

Synonyme

12EH9M7279 | CHEBI:27376 | CCRIS 2783 | EINECS 200-898-6 | NSC 3718 | methansulfonic acid | HSDB 5004 | 03S | METHANESULFONIC ACID [MI] | STL264182 | Q414168 | ammoniummethanesulfonate | MSA | NCGC00258626-01 | CH3SO3H | DL-MALICACIDMONOSODIUMSALT | METHA

Spezifikationen & Reinheit

UltraPureChrom™, for HPLC, ≥99.5%(T)

Storage

Room temperature

Verschickt in

FedEx DG Service

Note

for HPLC, UltraPureChrom™

Reinheit

≥99.5%(T)

Namen und Kennungen

Pubchem Sid

508814898

Kanonisches Lächeln

CS(=O)(=O)O

IUPAC Name

methanesulfonic acid

InChIKey

AFVFQIVMOAPDHO-UHFFFAOYSA-N

INCHI

1S/CH4O3S/c1-5(2,3)4/h1H3,(H,2,3,4)

Isomere SMILES

CS(=O)(=O)O

WGK Deutschland

1

RTECS

PB1140000

UN-Nummer

UN 1219

Verpackungsgruppe

II

Molekulargewicht

96.11

Beilstein

1446024

Reaxy-Rn

1446024

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1446024&ln=

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Klasse: Organic sulfonic acids and derivatives
• Subclass: Organosulfonic acids and derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Organosulfonic acids
• Alternative Parents: Sulfonyls Methanesulfonates Alkanesulfonic acids Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Alkanesulfonic acid - Sulfonyl - Organosulfonic acid - Methanesulfonate - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organosulfur compound - Aliphatic acyclic compound
• Beschreibung: 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: one-carbon compound - alkanesulfonic acid

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

Wirkungsmechanismen

Chemische und physikalische Eigenschaften

• Brechungsindex: 1.481 g/cm3
• Flammpunkt (°F): 372.2 °F
• Flammpunkt (°C): 189 °C
• Siedepunkt (°C): 167°C
• Schmelzpunkt (°C): 18 °C
• Molekulargewicht: 96.110 g/mol
• XLogP3: -0.900
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 0
• Exact Mass: 95.9881 Da
• Monoisotopic Mass: 95.9881 Da
• Topological Polar Surface Area: 62.800 Ų
• Heavy Atom Count: 5
• Formal Charge: 0
• Complexity: 92.600
• 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: 1