13-Diaminopropane

CAS No. 109-76-2

13-Diaminopropane( 13-Diaminopropane | 13-Propanediamine )

Catalog No. M19709 CAS No. 109-76-2

13-Diaminopropane is a common synthesis reagent used in the synthesis of cholinesterase inhibitors and thrombosis inhibitors.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
100MG Get Quote Get Quote
200MG Get Quote Get Quote
500MG Get Quote Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    13-Diaminopropane
  • Note
    Research use only, not for human use.
  • Brief Description
    13-Diaminopropane is a common synthesis reagent used in the synthesis of cholinesterase inhibitors and thrombosis inhibitors.
  • Description
    13-Diaminopropane is a common synthesis reagent used in the synthesis of cholinesterase inhibitors and thrombosis inhibitors.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    13-Diaminopropane | 13-Propanediamine
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    Others
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    109-76-2
  • Formula Weight
    74.12
  • Molecular Formula
    C3H10N2
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO:10 mM
  • SMILES
    NCCCN
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1.Ga V D B Muskiet F A Kingma A W et al. Simultaneous gas-chromatographic determination of free and acetyl-conjugated polyamines in urine.[J]. Clinical Chemistry 1986 32(10):1930-1937.
molnova catalog
related products
  • 8-Azabicyclo-3.2.1-o...

    Reference standards.

  • POPE

    POPE is a compound found in Escherichia coli, part of the cell membrane, and can be used to study changes in cell membrane permeability.

  • HLM006474

    HLM006474 is a pan inhibitor of E2F. This inhibits E2F4 DNA-binding (IC50: 29.8 μM in A375 cells).HLM006474 causes the viability of both SCLC and NSCLC lines (IC50 ranging from 15 to 75 μM). HLM006474 displays little activities against E2F4 DNA-binding in A375 cells at 10 and 20 μM, apparently inhibits E2F4 DNA-binding at 40 μM, and increasingly suppresses the effect at 60 and 80 μM concentrations.