1-Thioglycerol - für Zellkulturen, ≥97% , CAS No.96-27-5

CAS: 96-27-5 Cat. No.: T109442 Summenformel: C₃H₈O₂S Molekulargewicht: 108.16 Beilstein Registry Number: 1732046 EG-Nummer: 202-495-0 PubChem CID: 7291

GRADE & PURITY for Cell culture, ≥97%

Synonyms

NCGC00260427-01 | 1,2-Propanediol, 3-mercapto- | HSDB 2184 | D92320 | 2,3-Dihydroxypropanethiol | 3-Mercapto-1,2-propanediole | 3-Sulfanyl-1,2-propanediol # | CHEBI:74537 | NSC5370 | NSC-5370 | Monothioglycerol [NF] | Monothioglycerol (NF) | 1-Mercapto-2,

Storage

Lagerung bei 2-8°C, Argon geladen

Shipped In

Nasses Eis

Übersicht

In Zellkulturstudien mit embryonalen kortikalen und hippokampalen Neuronen, Mastzelllinien aus dem Knochenmark der Maus und menschlichen Β-Zelllinien wurde 1-Thioglycerin als Bestandteil des Kulturmediums zur Stimulierung der Proliferation verwendet.

Specifications

Synonyme

NCGC00260427-01 | 1,2-Propanediol, 3-mercapto- | HSDB 2184 | D92320 | 2,3-Dihydroxypropanethiol | 3-Mercapto-1,2-propanediole | 3-Sulfanyl-1,2-propanediol # | CHEBI:74537 | NSC5370 | NSC-5370 | Monothioglycerol [NF] | Monothioglycerol (NF) | 1-Mercapto-2,

Spezifikationen & Reinheit

für Zellkulturen, ≥97%

Storage

Lagerung bei 2-8°C, Argon geladen

Verschickt in

Nasses Eis

Note

für die Zellkultur

Reinheit

≥97%

Namen und Kennungen

• Pubchem Sid: 508807427
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/508807427
• Kanonisches Lächeln: C(C(CS)O)O
• IUPAC Name: 3-sulfanylpropane-1,2-diol
• InChIKey: PJUIMOJAAPLTRJ-UHFFFAOYSA-N
• INCHI: 1S/C3H8O2S/c4-1-3(5)2-6/h3-6H,1-2H2
• Isomere SMILES: C(C(CS)O)O
• WGK Deutschland: 3
• RTECS: TY8140000
• PubChem CID: 7291
• UN-Nummer: 2810
• Verpackungsgruppe: III
• Molekulargewicht: 108.16
• Beilstein: 1732046
• Reaxy-Rn: 1732046

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Klasse Organooxygen compounds
      • Subclass Alcohols and polyols
        • Ebene5 Polyols
          • Ebene6 1,2-diols

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Klasse: Organooxygen compounds
• Subclass: Alcohols and polyols
• Intermediate Tree Nodes: Polyols
• Direct Parent: 1,2-diols
• Alternative Parents: Secondary alcohols Alkylthiols Primary alcohols Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Secondary alcohol - 1,2-diol - Alkylthiol - Hydrocarbon derivative - Primary alcohol - Organosulfur compound - Aliphatic acyclic compound
• Beschreibung: This compound belongs to the class of organic compounds known as 1,2-diols. These are polyols containing an alcohol group at two adjacent positions.
• 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

Zugehörige Ziele (nicht menschlich)

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Wirkungsmechanismen

Chemische und physikalische Eigenschaften

• Empfindlichkeit: Moisture and Air sensitive
• Brechungsindex: n20/D 1.525-1.53
• Flammpunkt (°F): 210.2°F(lit.)
• Flammpunkt (°C): 99°C(lit.)
• Siedepunkt (°C): 118°C
• Molekulargewicht: 108.160 g/mol
• XLogP3: -0.800
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 2
• Exact Mass: 108.025 Da
• Monoisotopic Mass: 108.025 Da
• Topological Polar Surface Area: 41.500 Ų
• Heavy Atom Count: 6
• Formal Charge: 0
• Complexity: 32.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 1
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1