23304-08-7

Basic information

• Product Name: HEXAMETHYLENETETRAMINE-D12
• Synonyms: HEXAMETHYLENETETRAMINE-D12;1,3,5,7-Tetraazatricyclodecane-d12;Aceto HMT-d12;AMinoforM-d12;AMMoforM-d12;Antihydral-d12;Cystogen-d12;Duirexol-d12
• CAS NO: 23304-08-7
• Molecular Formula: C₆H₁₂N₄
• Molecular Weight: 152.26
• Product Categories: Heterocycles;Intermediates & Fine Chemicals;Isotope Labelled Compounds;Pharmaceuticals;Heterocycles, Isotope Labelled Compounds, Pharmaceuticals, Intermediates & Fine Chemicals
• Mol File: 23304-08-7.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: HEXAMETHYLENETETRAMINE-D12(CAS DataBase Reference)
• NIST Chemistry Reference: HEXAMETHYLENETETRAMINE-D12(23304-08-7)
• EPA Substance Registry System: HEXAMETHYLENETETRAMINE-D12(23304-08-7)

Safety Data

• Hazardous Substances Data: 23304-08-7(Hazardous Substances Data)

Usage

Uses

HexaMethylenetetraMine-d12 cna be used in the treatment of urinary track infection.

Upstream product

• 1664-98-8 paraformaldehyde-d2 

Relevant articles and documents

Deuterium Lineshape Study of Tetrahedral Jumps in Solid Hexamethylenetetramine

The reorientational motion of hexamethylenetetramine (HMT) in the solid has been studied by 2H NMR.Powder spectra were tahen by wideline techniques in the temperature interval T=368 to 448 K. the lineshape changes from the powder pattern of a rigid solid (Pake diagram) to a narrow line, the total width of the spectrum being reduced from 250 to less than 1 kHz.For intermediate temperatures the lineshape consists of a superposition of a broad absorption and a narrow central component of virtually temperature-independent width.The data are analyzed in terms of a stochastic model of tetrahedral jumps.A simple computer program for the numerical calculation of the powder lineshape is described.The correlation times τ, obtained from lineshape analysis, follow a simple Arrhenius plot with an activation energy ΔE=70.2+/-3 kJ/mol.Extrapolation to lower temperatures shows excellent agreement with the results of an earlier 14N relaxation study of Alexander and Tzalmona; the Arrhenius plot thus extends over at least five orders of magnitude from τ ca. 0.3 sec to τ ca. 3*10-6 sec.

Synthesizing method of deuterated octogen

The invention discloses a synthesizing method of deuterated octogen. The synthesizing method is characterized by comprising the following steps of enabling a deuterated formaldehyde matter and an ammonia compound to react, so as to obtain an intermediate, namely deuterated urotropine; further acetylizing and nitrifying, so as to obtain an intermediate, namely 1,5-diacetyl-3,7-binitro-1,3,5,7-teraazamacrocycle octane; using nitric acid/phosphorus pentoxide to nitrify, so as to obtain the product with high selectivity, namely deuterated octogen. The deuterated octogen synthesized by the method has the advantages that the purity is high, the deuterating rate is high, and the deuterated octogen can be applied to the fields of neutron diffraction, energetic material study, analysis and detection, and the like.