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Basic information

  • Name:
  • Methanamine,N-methyl-, hydrochloride (1:1)

  • Superlist Name:
  • Dimethylamine hydrochloride
  • CAS No.:
  • 506-59-2

  • Formula:
  • C2H7N.HCl
  • Synonyms:
  • Methanamine, N-methyl-, hydrochloride (9CI);Dimethylammonium chloride;
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Specification

The Dimethylamine HCl, with the CAS registry number 506-59-2, is also known as Dimethylammonium chloride. It belongs to the product categories of Amine Salts; Nitrogen Compounds; Organic Building Blocks. Its EINECS registry number is 208-046-5. This chemical's molecular formula is C2H8ClN and molecular weight is 81.54. What's more, both its IUPAC name and systematic name are the same which is called N-Methylmethanamine hydrochloride. This chemical can be prepared by Dimethylamine with Hydrochloric acid. 

Physical properties about Dimethylamine HCl are: (1)ACD/LogP: -0.43; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): -3.53; (4)ACD/LogD (pH 7.4): -3.33; (5)ACD/BCF (pH 5.5): 1; (6)ACD/BCF (pH 7.4): 1; (7)ACD/KOC (pH 5.5): 1; (8)ACD/KOC (pH 7.4): 1; (9)#H bond acceptors: 1; (10)#H bond donors: 1; (11)#Freely Rotating Bonds: 0; (12)Polar Surface Area: 3.24 Å2; (13)Enthalpy of Vaporization: 26.4 kJ/mol; (14)Boiling Point: 6.1 °C at 760 mmHg; (15)Vapour Pressure: 1520 mmHg at 25 °C.

Uses of Dimethylamine HCl: (1) it is used as catalysator of acetylation analysis, raw materials of pharmaceutical and organic synthesis; (2) it is used to produce other chemicals. For example, it can react with 1-Methyl-pyrrole, Formaldehyde to get Dimethyl-(1-methyl-pyrrol-2-ylmethyl)-amine. The reaction occurs with solvent H2O. The reaction time is 6 hours. The yield is 70 %.

Dimethylamine HCl can react with 1-Methyl-pyrrole, Formaldehyde to get Dimethyl-(1-methyl-pyrrol-2-ylmethyl)-amine.

When you are dealing with this chemical, you should be very careful. This chemical is irritating to eyes, respiratory system and skin. If swallowed, it's harmful to health. Therefore, you should wear suitable protective clothing, gloves and eye/face protection. And in case of contacting with eyes, you should rinse immediately with plenty of water and seek medical advice.

You can still convert the following datas into molecular structure:
(1) SMILES: Cl.N(C)C
(2) InChI: InChI=1S/C2H7N.ClH/c1-3-2;/h3H,1-2H3;1H
(3) InChIKey: IQDGSYLLQPDQDV-UHFFFAOYSA-N

The toxicity data is as follows:

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
guinea pig LD50 oral 1600mg/kg (1600mg/kg)   Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 32(6), Pg. 12, 1967.
mouse LD50 intraperitoneal 1570mg/kg (1570mg/kg) LUNGS, THORAX, OR RESPIRATION: RESPIRATORY STIMULATION Japanese Journal of Pharmacology. Vol. 17, Pg. 475, 1967.
Link to PubMed
mouse LD50 intravenous 1210mg/kg (1210mg/kg)   Archives Internationales de Pharmacodynamie et de Therapie. Vol. 112, Pg. 36, 1957.
Link to PubMed
mouse LD50 oral 8100mg/kg (8100mg/kg)   Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 32(6), Pg. 12, 1967.
mouse LD50 subcutaneous 2gm/kg (2000mg/kg)   Archives Internationales de Pharmacodynamie et de Therapie. Vol. 112, Pg. 36, 1957.
Link to PubMed
rabbit LD50 oral 1600mg/kg (1600mg/kg)   Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 32(6), Pg. 12, 1967.
rat LD50 oral 1070mg/kg (1070mg/kg)   Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 32(6), Pg. 12, 1967.

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