917-72-6

Basic information

• Product Name: DIMETHYLAMINE-N-D1
• Synonyms: DIMETHYLAMINE-N-D1;Dimethylamine-N-D1 (gas)
• CAS NO: 917-72-6
• Molecular Formula: C₂H₇N
• Molecular Weight: 46.09
• Mol File: 917-72-6.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• CAS DataBase Reference: DIMETHYLAMINE-N-D1(CAS DataBase Reference)
• NIST Chemistry Reference: DIMETHYLAMINE-N-D1(917-72-6)
• EPA Substance Registry System: DIMETHYLAMINE-N-D1(917-72-6)

Safety Data

• Hazardous Substances Data: 917-72-6(Hazardous Substances Data)

Upstream product

• 506-59-2 N,N-dimethylammonium chloride 
• 126191-35-3 2-(tert-Butylazo)-2(dimethylamino)propane 
• 124-40-3 dimethyl amine 
• 2386-98-3 bis(dimethylamino)borane 
• 10524-51-3 Tetrakis(dimethylamino)methan 

Downstream Products

• 124-40-3 dimethyl amine 
• 874197-30-5 Fe(NH(CH₃)2)(NC₅H₃(C(CH₂)NC₆H₃(CH(CH₃)2)2)2) 

Relevant articles and documents

SPECTROSCOPIC STUDY OF HYDROGEN BONDS IN DIMETHYLAMINE AND ITS DEUTERO ANALOGS IN THE TEMPERATURE RANGE OF 4-300 K

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Deuterated arglabin dimethylamine fumarate and preparation method thereof, and application of deuterated dimethylamine fumarate to drug preparation

The invention relates to deuterated arglabin dimethylamine fumarate with a structure as shown in a formula (I) which is described in the specification and a preparation method thereof, and applicationof deuterated arglabin dimethylamine fumarate to drug preparation.

Thermolysis, Photolysis, and Acid Catalysis of an α-(Dimethylamino)azoalkane. Amino Stabilization of a Carbon Radical Center

The unsymmetrical azoalkane 2-(tert-butylazo)-2-(dimethylamino)propane (7) has been synthesized cleanly by nucleophilic displacement of chloride from the corresponding α-chloroazoalkane 5 with dimethylamine.Thermolysis of 7 in hydrocarbon solvents affords typical radical-derived products and exhibits activation parameters ΔH(excit.) = 26.6 +/- 0.4 kcal/mol and ΔS(excit.) = -6.6 +/- 1.1 eu.Since the thermolysis rate of 7 is 104 faster than that of 1,2-di-tert-butyldiazene, the large stabilization of α-amino radicals is supported.Unusual products were obtained in acetonitrile, suggesting reduction of the azo linkage by 2-(dimethylamino)-2-propyl radicals and cleavage of the resulting hydrazyl radicals.In protic solvents, 7 undergoes acid catalyzed decomposition via tert-butyldiazene as a postulated intermediate.