Spermidine trihydrochloride - BioReagent, ≥99.5%(AT) , CAS No.334-50-9

CAS: 334-50-9 Cat. No.: S755657 Formula: N₃C₇H₂₂Cl₃ Peso molecolare: 254.63 Beilstein Registry Number: 3552356 Numero EC: 206-379-0 PubChem CID: 9539

GRADE & PURITY BioReagent, ≥99.5%(AT)

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Panoramica

Spermidine trihydrochloride is an aliphatic polyamine. Its crystalline structure has been studied. It has been reported to preserve the nuclei and prevent proteolytic degradation of histones during the macronuclei isolation from Tetrahymena pyriformis.

Application:

Spermidine trihydrochloride is used for the following applications:

• DNA extraction and restriction endonuclease digestion
• Nuclear transplantation
• During the chemical analyses of the squid species Todaropsis eblanae
• As one of the agents in intercalating drug.
• Platelet aggregation

It may be used in the synthesis of palladium complexes like [sperH₃]₂[PdCl₄]₃, [PdCl₂(sperH)]₂[PdCl₄], and [(PdCl₂)₃(sper)₂] by reacting with K₂PdCl₄ and PdCl₂.

Specifications

Specifiche e purezza

BioReagent, ≥99.5%(AT)

Meccanismi biochimici e fisiologici

Inhibits neuronal nitric oxide synthase (nNOS). Binds and precipitates DNA; may be used for purification of DNA binding proteins. Stimulates T4 polynucleotide kinase activity.

Condizioni di conservazione di stoccaggio

Store at 2-8°C,Argon charged

Spedito in

Wet ice

Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.

Grado

BioReagent

Purezza

≥99.5%(AT)

Nomi e identificatori

Pubchem Sid

528769853

PH

3.0-6.0 (25 °C, 1 M in H 2 O)

Sorrisi canonici

C(CCNCCCN)CN.Cl.Cl.Cl

IUPAC Name

N'-(3-aminopropyl)butane-1,4-diamine;trihydrochloride

InChIKey

LCNBIHVSOPXFMR-UHFFFAOYSA-N

INCHI

1S/C7H19N3.3ClH/c8-4-1-2-6-10-7-3-5-9;;;/h10H,1-9H2;3*1H

Isomeri SMILES

C(CCNCCCN)CN.Cl.Cl.Cl

WGK Germania

3

RTECS

EJ7023000

PubChem CID

9539

Peso molecolare

254.63

Beilstein

3552356

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic nitrogen compounds
    • Classe Organonitrogen compounds
      • Subclass Amines
        • Level5 Secondary amines
          • Level6 Dialkylamines

• Kingdom: Organic compounds
• Superclass: Organic nitrogen compounds
• Classe: Organonitrogen compounds
• Subclass: Amines
• Intermediate Tree Nodes: Secondary amines
• Direct Parent: Dialkylamines
• Alternative Parents: Organopnictogen compounds Monoalkylamines Hydrochlorides Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Secondary aliphatic amine - Organopnictogen compound - Hydrocarbon derivative - Hydrochloride - Primary amine - Primary aliphatic amine - Aliphatic acyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as dialkylamines. These are organic compounds containing a dialkylamine group, characterized by two alkyl groups bonded to the amino nitrogen.
• 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: 1 M at 20 °C, clear, colorless
• Punto di fusione (°C): 257-259 °C
• Peso molecolare: 254.600 g/mol
• Hydrogen Bond Donor Count: 6
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 7
• Exact Mass: 253.088 Da
• Monoisotopic Mass: 253.088 Da
• Topological Polar Surface Area: 64.099 Ų
• Heavy Atom Count: 13
• Formal Charge: 0
• Complexity: 56.800
• 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: 4

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