Welcome to LookChem.com Sign In|Join Free

CAS

  • or
N,N'-Dicyanoethyl-1,4-butanediamine, also known as CAS number 14209-32-6, is a colorless oil compound that is useful in organic synthesis. It is characterized by its dicyanoethyl and butanediamine functional groups, which contribute to its chemical properties and potential applications in various industries.

14209-32-6 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 14209-32-6 Structure
  • Basic information

    1. Product Name: N,N'-DICYANOETHYL-1,4-BUTANEDIAMINE
    2. Synonyms: N,N'-DICYANOETHYL-1,4-BUTANEDIAMINE;3,3'-(1,4-ButanediyldiiMino)bis-propanenitrile;3,3'-(TetraMethylenediiMino)di-propionitrile;N,Na€-Dicyanoethyl-1,4-butanediamine
    3. CAS NO:14209-32-6
    4. Molecular Formula: C10H18N4
    5. Molecular Weight: 194.28
    6. EINECS: N/A
    7. Product Categories: Miscellaneous Reagents
    8. Mol File: 14209-32-6.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 187-196°C@0.7mm
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 0.981±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: Chloroform, Methanol,
    9. PKA: 8.82±0.19(Predicted)
    10. CAS DataBase Reference: N,N'-DICYANOETHYL-1,4-BUTANEDIAMINE(CAS DataBase Reference)
    11. NIST Chemistry Reference: N,N'-DICYANOETHYL-1,4-BUTANEDIAMINE(14209-32-6)
    12. EPA Substance Registry System: N,N'-DICYANOETHYL-1,4-BUTANEDIAMINE(14209-32-6)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 14209-32-6(Hazardous Substances Data)

14209-32-6 Usage

Uses

Used in Organic Synthesis:
N,N'-Dicyanoethyl-1,4-butanediamine is used as a synthetic building block for the creation of various organic compounds. Its unique structure allows it to be a versatile component in the synthesis of a wide range of molecules, including pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, N,N'-Dicyanoethyl-1,4-butanediamine is used as an intermediate in the synthesis of various drug molecules. Its ability to form stable complexes with other compounds makes it a valuable asset in the development of new medications with improved efficacy and reduced side effects.
Used in Agrochemical Industry:
N,N'-Dicyanoethyl-1,4-butanediamine is also utilized in the agrochemical industry for the synthesis of active ingredients in pesticides and other crop protection products. Its incorporation into these compounds can enhance their performance, leading to more effective and targeted pest control solutions.
Used in Specialty Chemicals Industry:
In the specialty chemicals industry, N,N'-Dicyanoethyl-1,4-butanediamine is employed as a key component in the development of advanced materials with specific properties. These materials can be used in various applications, such as coatings, adhesives, and polymers, where their unique characteristics provide advantages over traditional materials.

Check Digit Verification of cas no

The CAS Registry Mumber 14209-32-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,2,0 and 9 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 14209-32:
(7*1)+(6*4)+(5*2)+(4*0)+(3*9)+(2*3)+(1*2)=76
76 % 10 = 6
So 14209-32-6 is a valid CAS Registry Number.

14209-32-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,3'-(1,4-Butanediyldiimino)dipropanenitrile

1.2 Other means of identification

Product number -
Other names piperazine-1,4-dipropiononitrile

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:14209-32-6 SDS

14209-32-6Relevant articles and documents

Aqueous aza-michael reaction of conjugated alkenes: Toward spermine

Joshi, Jigar H.,Saiyed, Akeel S.,Bedekar, Ashutosh V.

, p. 2857 - 2863 (2010)

An aqueous aza-Michael reaction is efficiently achieved with excellent conversions without any additives. The method works very well on a molar scale with selectively for aliphatic amines. An intermediate for spermine is also made by this green process.

Discovery of novel alkylated (bis)urea and (bis)thiourea polyamine analogues with potent antimalarial activities

Verlinden, Bianca K.,Niemand, Jandeli,Snyman, Janette,Sharma, Shiv K.,Beattie, Ross J.,Woster, Patrick M.,Birkholtz, Lyn-Marie

, p. 6624 - 6633 (2011)

A series of alkylated (bis)urea and (bis)thiourea polyamine analogues were synthesized and screened for antimalarial activity against chloroquine-sensitive and -resistant strains of Plasmodium falciparum in vitro. All analogues showed growth inhibitory ac

Synthesis and biological evaluation of s-triazine substituted polyamines as potential new anti-Trypanosomal drugs

Klenke,Stewart,Barrett,Brun,Gilbert

, p. 3440 - 3452 (2001)

The P2 transporter is a nucleoside transporter which is unique to the protozoan parasite Trypanosoma brucei, the causative organism of Human African Trypanosomasis. The transporter has been shown to bind some structural motifs not recognized by other tran

Syntheses of a library of molecules on the marine natural product ianthelliformisamines platform and their biological evaluation

Khan, Faiz Ahmed,Ahmad, Saeed,Kodipelli, Naveena,Shivange, Gururaj,Anindya, Roy

, p. 3847 - 3865 (2014/06/09)

Ianthelliformisamines A-C are a novel class of bromotyrosine-derived antibacterial agents isolated recently from the marine sponge Suberea ianthelliformis. We have synthesized ianthelliformisamines A-C straightforwardly by the condensation of (E)-3-(3,5-dibromo-4-methoxyphenyl)acrylic acid and the corresponding Boc-protected polyamine followed by Boc-deprotection with TFA. Further, using this reaction protocol, a library of their analogues (39 analogues) has been synthesized by employing 3-phenylacrylic acid derivatives and Boc-protected polyamine chains through various combinations of these two fragments differing in phenyl ring substitution, double bond geometry or chain length of the central spacer of the polyamine chain (shown in red color). All the synthesized compounds (ianthelliformisamines A-C and their analogues) were screened for antibacterial activity against both Gram-negative (Escherichia coli) and Gram-positive (Staphylococcus aureus) strains. All synthetic analogues of ianthelliformisamine A showed bacterial growth inhibition against both strains (Escherichia coli and Staphylococcus aureus), having MIC values in the range of 117.8-0.10 μM, while none of the synthetic analogues of ianthelliformisamine C as well as the parent compound showed any detectable antibacterial activity. Interestingly, some of the synthetic analogues of ianthelliformisamines A and B exerted a bactericidal effect against both E. coli and S. aureus strains, decreasing viable bacterial count by 99% at concentrations as low as 2 × MIC. This journal is the Partner Organisations 2014.

Polyamine functionalized carbon nanotubes: Synthesis, characterization, cytotoxicity and siRNA binding

Singh, Prabhpreet,Samori, Cristian,Toma, Francesca Maria,Bussy, Cyrill,Nunes, Antonio,Al-Jamal, Khuloud T.,Menard-Moyon, Cecilia,Prato, Maurizio,Kostarelos, Kostas,Bianco, Alberto

supporting information; experimental part, p. 4850 - 4860 (2011/10/09)

In this work we have synthesized a new series of cationic carbon nanotubes (CNTs) for siRNA binding. Both single- and multi-walled CNTs have been modified by addition or amidation reaction with short linear polyamine chains including putrescine, spermidin

(Bis)urea and (Bis)thiourea inhibitors of lysine-specific demethylase 1 as epigenetic modulators

Sharma, Shiv K.,Wu, Yu,Steinbergs, Nora,Crowley, Michael L.,Hanson, Allison S.,Casero, Robert A.,Woster, Patrick M.

scheme or table, p. 5197 - 5212 (2010/09/09)

The recently discovered enzyme lysine-specific demethylase 1 (LSD1) plays an important role in the epigenetic control of gene expression, and aberrant gene silencing secondary to LSD1 overexpression is thought to contribute to the development of cancer. W

ESTER-LINKED GEMINI SURFACTANT COMPOUNDS FOR USE IN GENE THERAPY

-

Page/Page column 9, (2008/06/13)

This invention relates to newly identified ester-linked gemini surfactant compounds of formula (I), where Y is either H or (Aa)x where (Aa) is a basic amino acid and x is 1 to 6, to the use of such compounds and to their production. The invention also relates to the use of the ester-linked gemini surfactant compounds to facilitate the transfer of polynucleotide into cells.

NEW ADJUVANT

-

Page/Page column 56; 57, (2010/11/25)

The present invention provides a novel adjuvant for polynucleotide vaccines, and in particular the present invention provides immunogenic compositions comprising a polynucleotide encoding an antigen capable of eliciting an immune response and an adjuvant

Solid-phase synthesis of diamine and polyamine amino acid derivatives as HIV-1 Tat-TAR binding inhibitors

Bueno, G. Jimenez,Klimkait,Gilbert,Simons

, p. 87 - 94 (2007/10/03)

A series of diamine and polyamine derivatives, either free amines or salts (HCl or TFA), of aspartic and glutamic acid were prepared in excellent yields using Rink Amide solid-phase synthesis. The asparagine and glutamine derivatives were all evaluated for their ability to inhibit Tat-TAR binding using a FIGS cellular assay, with the polyamine derivatives exhibiting the most promising binding activity.

Sinulamide: An H,K-ATPase inhibitor from a soft coral Sinularia sp.

Sata, Noriko U.,Sugano, Michihiro,Matsunaga, Shigeki,Fusetani, Nobuhiro

, p. 719 - 722 (2007/10/03)

Sinulamide (1), a new tetraprenylated spermine derivative, has been isolated from a soft coral Sinularia sp. as an H,K-ATPase inhibitor. The structure was assigned on the basis of spectroscopic data and confirmed by a total synthesis.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 14209-32-6