Dimethyl sulfoxide-d₆ - anhydrous, ≥99.9 atom% D , CAS No.2206-27-1

CAS: 2206-27-1 Cat. No.: D432339 Formula: C₂D₆SO Peso molecolare: 84.17 Beilstein Registry Number: 1237248 Numero EC: 218-617-0

GRADE & PURITY Anhydrous Grade, ≥99.9 atom% D

Synonyms

Agermin | MFCD00002090 | Dimethyl sulfoxide-d6, 'Special HOH', >=99.9 atom % D | Dimethicone 350 | Hexadeuteriodimethyl sulfoxide | Dimethyl sulfoxide-d6, Vetec(TM) reagent grade, 99.8 atom % D, contains 0.03 % (v/v) TMS | DIMETHYL SULFOXIDE-D6 99.9ATOM%D

Storage

Protected from light,Room temperature,Argon charged

Shipped In

Normal

Panoramica

Dimethyl sulfoxide-d 6 (DMSO-d 6 ) is a deuterated NMR solvent. It undergoes photodissociation to generate CD 3 radical photoproducts, which have been analyzed by infrared diode laserabsorption spectroscopy. Dissociation dynamics of DMSO-d 6 at 193nm was examined using photo fragment translational spectroscopy method.

Application

Dimethyl sulfoxide-d 6 may be used as an NMR solvent for 1 H and 13 C NMR experiments.

Specifications

Sinonimi

Agermin | MFCD00002090 | Dimethyl sulfoxide-d6, 'Special HOH', >=99.9 atom % D | Dimethicone 350 | Hexadeuteriodimethyl sulfoxide | Dimethyl sulfoxide-d6, Vetec(TM) reagent grade, 99.8 atom % D, contains 0.03 % (v/v) TMS | DIMETHYL SULFOXIDE-D6 99.9ATOM%D

Specifiche e purezza

anhydrous, ≥99.9 atom% D

Condizioni di conservazione di stoccaggio

Protected from light,Room temperature,Argon charged

Spedito in

Normal

Grado

Anhydrous Grade

Purezza

≥99.9 atom% D

Nomi e identificatori

Pubchem Sid

504754917

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/504754917

Sorrisi canonici

[2H]C([2H])([2H])S(=O)C([2H])([2H])[2H]

IUPAC Name

trideuterio(trideuteriomethylsulfinyl)methane

InChIKey

IAZDPXIOMUYVGZ-WFGJKAKNSA-N

INCHI

1S/C2H6OS/c1-4(2)3/h1-2H3/i1D3,2D3

Isomeri SMILES

[2H]C([2H])([2H])S(=O)C([2H])([2H])[2H]

WGK Germania

2

CAS alternativo

67-68-5（Unlabeled）

Peso molecolare

84.17

Beilstein

1237248

Reaxy-Rn

1237248

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1237248&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organosulfur compounds
    • Classe Sulfoxides

• Kingdom: Organic compounds
• Superclass: Organosulfur compounds
• Classe: Sulfoxides
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Sulfoxides
• Alternative Parents: Sulfinyl compounds Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Sulfoxide - Sulfinyl compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Aliphatic acyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as sulfoxides. These are compounds containing a sulfoxide functional group, with the structure RS(=O)R' (R,R' not H).
• 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

Proprietà chimiche e fisiche

• Punto di congelamento (°C): 20 °C
• Indice di rifrazione: 1.48
• Punto di infiammabilità (°F): 190.4 °F
• Punto di infiammabilità (°C): 88℃
• Punto di ebollizione (°C): 190°C
• Punto di fusione (°C): 20°C
• Peso molecolare: 84.170 g/mol
• XLogP3: -0.600
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 0
• Exact Mass: 84.0516 Da
• Monoisotopic Mass: 84.0516 Da
• Topological Polar Surface Area: 36.300 Ų
• Heavy Atom Count: 4
• Formal Charge: 0
• Complexity: 29.000
• Isotope Atom Count: 6
• 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