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

CAS: 75-75-2 Cat. No.: M433628 Formula: CH₄O₃S Peso molecolare: 96.11 Beilstein Registry Number: 1446024 Numero EC: 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

Sinonimi

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

Specifiche e purezza

UltraPureChrom™, for HPLC, ≥99.5%(T)

Condizioni di conservazione di stoccaggio

Room temperature

Spedito in

FedEx DG Service

Grado

for HPLC, UltraPureChrom™

Purezza

≥99.5%(T)

Nomi e identificatori

Pubchem Sid

508814898

Sorrisi canonici

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)

Isomeri SMILES

CS(=O)(=O)O

WGK Germania

1

RTECS

PB1140000

Numero UN

UN 1219

Gruppo di imballaggio

II

Peso molecolare

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
    • Classe Organic sulfonic acids and derivatives
      • Subclass Organosulfonic acids and derivatives

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Classe: 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
• Descrizione: 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

Meccanismi d'azione

Proprietà chimiche e fisiche

• Indice di rifrazione: 1.481 g/cm3
• Punto di infiammabilità (°F): 372.2 °F
• Punto di infiammabilità (°C): 189 °C
• Punto di ebollizione (°C): 167°C
• Punto di fusione (°C): 18 °C
• Peso molecolare: 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