Dimethyl sulfoxide（DMSO） - sterile-filtered, BioReagent, suitable for hybridoma, ≥99.7% , CAS No.67-68-5

CAS: 67-68-5 Cat. No.: D755829 Formula: C₂H₆SO Molecular Weight: 78.13 Beilstein Registry Number: 506008 EC Number: 200-664-3

GRADE & PURITY Sterile-filtered, BioReagent, Suitable for hybridoma, ≥99.7%

Storage

Room temperature,Argon charged

Shipped In

Normal

Overview

DMSO is a polar aprotic solvent used in chemical reactions, in polymerase chain reactions (PCR) and as a cryoprotectant vitrification agent for the preservation of cells, tissues and organs. DMSO is used in cell freezing media to protect cells from ice crystal induced mechanical injury. It is used for frozen storage of primary, sub-cultured, and recombinant heteroploid and hybridoma cell lines; embryonic stem cells (ESC), and hematopoietic stem cells. DMSO is frequently used in the combinations with BSA or fetal bovine serum (FBS).

Specifications

Specifications & Purity

sterile-filtered, BioReagent, suitable for hybridoma, ≥99.7%

Storage

Room temperature,Argon charged

Shipped In

Normal

Grade

BioReagent, Sterile-filtered, Suitable for hybridoma

Purity

≥99.7%

Names and Identifiers

Canonical Smiles

CS(=O)C

IUPAC Name

methylsulfinylmethane

InChIKey

IAZDPXIOMUYVGZ-UHFFFAOYSA-N

INCHI

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

Isomeric SMILES

CS(=O)C

WGK Germany

1

RTECS

PV6210000

Molecular Weight

78.13

Beilstein

506008

Reaxy-Rn

506008

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=506008&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organosulfur compounds
    • Class Sulfoxides

• Kingdom: Organic compounds
• Superclass: Organosulfur compounds
• Class: 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
• Description: 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: a small molecule

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

Chemical and Physical Properties

• Solubility: H 2 O: miscible (completely)
• Sensitivity: Moisture sensitive
• Refractive Index: 1.477-1.48
• Flash Point(°F): 189 °F
• Flash Point(°C): 87℃
• Boil Point(°C): 189°C
• Melt Point(°C): 16-19 °C (lit.)
• Molecular Weight: 78.140 g/mol
• XLogP3: -0.600
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 0
• Exact Mass: 78.0139 Da
• Monoisotopic Mass: 78.0139 Da
• Topological Polar Surface Area: 36.300 Ų
• Heavy Atom Count: 4
• Formal Charge: 0
• Complexity: 29.000
• 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: 1