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Molecular Formula: C2H8ClN
Molecular Weight: 81.54
EINECS: 208-046-5
Purity: 97% Min.
Package: 5 g / 25 g / 1 kg / 25 kg
Introduction
Dimethylamine hydrochloride is a raw material for organic synthesis.
It is also used as a catalyst and magnesium reagent for acetylation analysis. Dimethylamine hydrochloride has been used in the preparation of hexamethylmelamine-methyl-14C.
It has also been used to prepare the standard solution of methylamine (MA), dimethylamine (DMA), trimethylamine (TMA), and trimethylamine-N-oxide (TMAO) while determing methylamines and trimethylamine-N-oxide in particulate matter. Dimethylamine hydrochloride is used as an intermediate in the manufacture of pharmaceuticals like ranitidine and metformin, amlodipine. It is used as a precursor of atrazine. It is associated with sodium acetate and used to carry out the Willgerodt- Kindler reaction to prepare amides. Its free base reacts with carbon disulfide to get dimethyldithiocarbamate which is used in rubber vulcanization. It is involved in the synthesis of dimethyl-(1-methyl-pyrrol-2-ylmethyl)-amine by reacting with 1-methyl pyrrole and formaldehyde.
SPECIFICATION OF CAS: 506-59-2 Dimethylamine hydrochloride
ITEMS | SPECIFICATION |
Melting point | 170-173 ¡ãC(lit.) |
InChIKey | IQDGSYLLQPDQDV-UHFFFAOYSA-N |
solubility | H2O |
storage temp. | Store below +30¡ãC. |
Merck | 14,3228 |
color | White to off-white |
vapor pressure | <0.1 hPa (25 ¡ãC) |
Form | Crystalline Powder or Crystals |
EPA Substance Registry System | Methanamine, N-methyl-, hydrochloride (506-59-2) |
Density | 0.8949 |
Stability | Stable. Incompatible with strong oxidizing agents. |
Boiling point | 95.79¡ã°ä&²Ô²ú²õ±è; |
Water Solubility | 3000 g/L (20 oC) |
Sensitive | Hygroscopic |
refractive index | 1.4202 |
BRN | 3589311 |
PH | 5 (100g/l, H2O, 20¡æ) |
CAS DataBase Reference | 506-59-2(CAS DataBase Reference) |
Synthesis of CAS: 506-59-2 Dimethylamine hydrochloride
With dichloromethane; hydrogen; palladium on activated charcoal In methanol at 20¡æ; for 24h; atmospheric pressure;
Reference:
Wang, Xinyan; Dong, Yanmei; Sun, Jianwei; Xu, Xuenong; Li, Rui; Hu, Yuefei [Journal of Organic Chemistry, 2005, vol. 70, # 5, p. 1897 - 1900]
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