Trimethylsulfonium hydroxide solution - 0.2mol/L in methanol , CAS No.17287-03-5

CAS: 17287-03-5 Cat. No.: T113600 Peso molecular: 94.18 Beilstein Registry Number: 3910286 Número EC: 628-493-3 PubChem CID: 11105313

GRADE & PURITY 0.2mol/L in methanol

Synonyms

DTXSID70938225 | Trimethylsulfoniumhydroxyd | UNII-835839L58Y | IODO-GLUTIONAL [WHO-DD] | Trimethylsulfanium Hydroxide | T1576 | trimethylsulfanium;hydroxide | 835839L58Y | MFCD00216756 | MDTPTXSNPBAUHX-UHFFFAOYSA-M | Sulfonium, trimethyl-, hydroxide | AI

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

Descripción general

Trimethylsulfonium hydroxide (TMSH) is a methylating reagent. It can be prepared by dissolving trimethylsulfonium iodide in methanol and water solvent further treating with silver oxide.

Specifications

Sinónimos

DTXSID70938225 | Trimethylsulfoniumhydroxyd | UNII-835839L58Y | IODO-GLUTIONAL [WHO-DD] | Trimethylsulfanium Hydroxide | T1576 | trimethylsulfanium;hydroxide | 835839L58Y | MFCD00216756 | MDTPTXSNPBAUHX-UHFFFAOYSA-M | Sulfonium, trimethyl-, hydroxide | AI

Especificaciones y pureza

0.2mol/L in methanol

Condiciones de almacenamiento de almacenamiento

Store at -20°C

Enviado en

Ice chest + Ice pads

Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.

Nombres e identificadores

• Pubchem Sid: 504766009
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504766009
• Sonrisas canónicas: C[S+](C)C.[OH-]
• IUPAC Name: trimethylsulfanium;hydroxide
• InChIKey: MDTPTXSNPBAUHX-UHFFFAOYSA-M
• INCHI: 1S/C3H9S.H2O/c1-4(2)3;/h1-3H3;1H2/q+1;/p-1
• Isómeros SMILES: C[S+](C)C.[OH-]
• WGK Alemania: 2
• PubChem CID: 11105313
• Número ONU: 3286
• Peso molecular: 94.18
• Beilstein: 3910286
• Reaxy-Rn: 3910286

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Clase Organic oxoanionic compounds

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Clase: Organic oxoanionic compounds
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Organic oxoanionic compounds
• Alternative Parents: Organosulfur compounds Organic salts Organic oxides Hydrocarbon derivatives Organic cations
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Organic oxide - Hydrocarbon derivative - Organic salt - Organosulfur compound - Organic hydroxide - Organic cation - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as organic oxoanionic compounds. These are organic compounds containing an oxoanion.
• 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

• Sensibilidad: heat sensitive
• Punto de inflamación (°F): 11℃
• Punto de inflamación (°C): 11℃
• Peso molecular: 94.180 g/mol
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 94.0452 Da
• Monoisotopic Mass: 94.0452 Da
• Topological Polar Surface Area: 2.000 Ų
• Heavy Atom Count: 5
• Formal Charge: 0
• Complexity: 8.000
• 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

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