1. Home
  2. 1,4-Butanediamine, N,N'-dimethyl-

Contact Angene

Tel: +852 8191 6999

Email: sales@angenechemical.com

Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

1,4-Butanediamine, N,N'-dimethyl-

CNCCCCNC Request for Quotation
Chemical Name: 1,4-Butanediamine, N,N'-dimethyl-
CAS Number: 16011-97-5
Product Number: AG001ROI(AGN-PC-0JLVKB)
Synonyms:
MDL No: MFCD00039799
Molecular Formula: C6H16N2
Molecular Weight: 116.2046

Identification/Properties

Properties
BP:
158.8°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Liquid
Computed Properties
Molecular Weight:
116.208g/mol
XLogP3:
0.1
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
5
Exact Mass:
116.131g/mol
Monoisotopic Mass:
116.131g/mol
Topological Polar Surface Area:
24.1A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
31.5
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


N,N'-Dimethyl-1,4-butanediamine, commonly referred to as DMBD, is a versatile compound widely used in chemical synthesis. Its primary application lies in its role as a bifunctional amine, making it a valuable building block for the preparation of various organic compounds.In chemical synthesis, DMBD serves as an efficient reagent for the formation of amide linkages, which are prevalent in the synthesis of peptides, pharmaceuticals, and other biologically active molecules. Due to its unique structure, DMBD enables precise control over the formation of amide bonds, allowing chemists to create complex structures with high yield and purity.Additionally, N,N'-Dimethyl-1,4-butanediamine finds use in the synthesis of polymers, where it functions as a chain extender or crosslinking agent. Its ability to form stable linkages between polymer chains enhances the mechanical and thermal properties of the resulting materials, making it indispensable in the production of specialty polymers with tailored properties.Overall, the versatility and reliability of N,N'-Dimethyl-1,4-butanediamine make it a valuable tool in organic synthesis, enabling chemists to efficiently construct intricate molecules and materials with precision and control.