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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)-

1,3-Butanediamine, N,N,N',N'-tetramethyl-

CN(CCC(N(C)C)C)C Request for Quotation
Chemical Name: 1,3-Butanediamine, N,N,N',N'-tetramethyl-
CAS Number: 97-84-7
Product Number: AG003SGL(AGN-PC-0JK81Q)
Synonyms:
MDL No:
Molecular Formula: C8H20N2
Molecular Weight: 144.2578

Identification/Properties

Properties
BP:
165.0°C

Safety Information

GHS Pictogram:
Signal Word:
Danger
UN#:
2733
Hazard Statements:
H226-H302-H311-H314-H332
Precautionary Statements:
P280-P305+P351+P338-P310
Class:
3,8
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


The application of N,N,N',N'-tetramethyl-1,3-butanediamine in chemical synthesis is crucial for various organic reactions. This compound serves as a strong organic base due to the presence of four methyl groups attached to the nitrogen atoms, which enhances its basicity and nucleophilicity. N,N,N',N'-tetramethyl-1,3-butanediamine is commonly used as a catalyst in the formation of carbon-carbon bonds, especially in the synthesis of pharmaceuticals, agrochemicals, and functional materials. Its high reactivity and stability make it a versatile reagent in organic transformations such as Michael additions, aldol reactions, and Knoevenagel condensations. Additionally, this compound is employed in the preparation of polymers, coordination complexes, and asymmetric synthesis processes, highlighting its significance in modern chemical research and development.