Cystamine dihydrochloride - UltraBio™ , CAS No.56-17-7

CAS: 56-17-7 Cat. No.: C755572 Formula: C₄H₁₂N₂S₂·2HCl Peso molecolare: 225.19 Numero EC: 200-260-7 PubChem CID: 5941

GRADE & PURITY UltraBio™

Storage

Room temperature

Shipped In

Normal

Panoramica

Cystamine dihydrochloride is a useful reagent to derivatize various polymer monoliths for hydrophilic interaction liquid chromatography; as a crosslinking agent in the development of polymer hydrogels; and as a functional group in nanoparticles developed for siRNA and DNA delivery.

Specifications

Specifiche e purezza

UltraBio™

Condizioni di conservazione di stoccaggio

Room temperature

Spedito in

Normal

Grado

UltraBio™

Nomi e identificatori

Sorrisi canonici

C(CSSCCN)N.Cl.Cl

IUPAC Name

2-(2-aminoethyldisulfanyl)ethanamine;dihydrochloride

InChIKey

YUFRRMZSSPQMOS-UHFFFAOYSA-N

INCHI

1S/C4H12N2S2.2ClH/c5-1-3-7-8-4-2-6;;/h1-6H2;2*1H

Isomeri SMILES

C(CSSCCN)N.Cl.Cl

WGK Germania

3

RTECS

KR7260000

PubChem CID

5941

Peso molecolare

225.19

Reaxy-Rn

3616850

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organosulfur compounds
    • Classe Organic disulfides
      • Subclass Dialkyldisulfides

• Kingdom: Organic compounds
• Superclass: Organosulfur compounds
• Classe: Organic disulfides
• Subclass: Dialkyldisulfides
• Intermediate Tree Nodes: Not available
• Direct Parent: Dialkyldisulfides
• Alternative Parents: Sulfenyl compounds Organopnictogen compounds Monoalkylamines Hydrochlorides Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Dialkyldisulfide - Sulfenyl compound - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Hydrochloride - Primary amine - Organonitrogen compound - Primary aliphatic amine - Amine - Aliphatic acyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as dialkyldisulfides. These are organic compounds containing a disulfide group R-SS-R' where R and R' are both alkyl groups.
• 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

• Solubilità: H 2 O: 0.1 M, clear, colorless to light yellow
• Punto di fusione (°C): 218 °C
• Peso molecolare: 225.200 g/mol
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 5
• Exact Mass: 223.998 Da
• Monoisotopic Mass: 223.998 Da
• Topological Polar Surface Area: 103.000 Ų
• Heavy Atom Count: 10
• Formal Charge: 0
• Complexity: 37.000
• 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: 3

XLogP3