Methylamine hydrochloride

Suppliers

Names

[ CAS No. ]:
593-51-1

[ Name ]:
Methylamine hydrochloride

[Synonym ]:
methanamine hydrochloride
Methyl-ammonium
metylamine hydrochloride
Methanamine, hydrochloride (1:1)
METHYLAMINE HCL
MONOMETHYLAMINE HCL
methylammonium chloride
Methanaminium chloride
Methylamine hydrochl
Methaniminium
Methylamine hydrochloride
EINECS 209-795-0
Methylaminium
MFCD00012849
Methylammonium Cloride
methyl amine hydrochloride
methylamine monohydrochloride
Methaneaminium
Methylammoniumchlorid

Chemical & Physical Properties

[ Boiling Point ]:
225-230 °C15 mm Hg(lit.)

[ Melting Point ]:
231-233 °C(lit.)

[ Molecular Formula ]:
CH6ClN

[ Molecular Weight ]:
67.518

[ Flash Point ]:
225-230°C/15mm

[ Exact Mass ]:
67.018875

[ PSA ]:
26.02000

[ LogP ]:
1.07720

[ Stability ]:
Stable, but may be moisture sensitive. Incompatible with strong oxidizing agents.

[ Water Solubility ]:
soluble

MSDS

Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
PA0603000
CHEMICAL NAME :
Methanamine, hydrochloride
CAS REGISTRY NUMBER :
593-51-1
LAST UPDATED :
199710
DATA ITEMS CITED :
7
MOLECULAR FORMULA :
C-H5-N.Cl-H
MOLECULAR WEIGHT :
67.53

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
1600 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
INHTE5 Inhalation Toxicology. (Hemisphere Publishing Corp., c/o Taylor & Francis Inc., 1900 Frost Rd., Suite 101, Bristol, PA 19007) V.1- 1989- Volume(issue)/page/year: 2,29,1990
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
2160 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
YKKZAJ Yakugaku Zasshi. Journal of Pharmacy. (Nippon Yakugakkai, 2-12-15 Shibuya, Shibuya-ku, Tokyo 150, Japan) No.1- 1881- Volume(issue)/page/year: 97,1117,1977
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Administration onto the skin
SPECIES OBSERVED :
Rodent - guinea pig
DOSE/DURATION :
>2 gm/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
KODAK* Kodak Company Reports. (343 State St., Rochester, NY 14650) Volume(issue)/page/year: 21MAY1971 ** OTHER MULTIPLE DOSE TOXICITY DATA **
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
610 mg/kg/5D-I
TOXIC EFFECTS :
Blood - changes in leukocyte (WBC) count
REFERENCE :
JTEHD6 Journal of Toxicology and Environmental Health. (Hemisphere Pub., 1025 Vermont Ave., NW, Washington, DC 20005) V.1- 1975/76- Volume(issue)/page/year: 47,479,1996 *** NIOSH STANDARDS DEVELOPMENT AND SURVEILLANCE DATA *** NIOSH OCCUPATIONAL EXPOSURE SURVEY DATA : NOES - National Occupational Exposure Survey (1983) NOES Hazard Code - X4270 No. of Facilities: 7 (estimated) No. of Industries: 1 No. of Occupations: 1 No. of Employees: 28 (estimated)

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H302-H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xn:Harmful

[ Risk Phrases ]:
R22;R36/37/38

[ Safety Phrases ]:
S26-S37/39

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
1

[ RTECS ]:
PA0603000

[ HS Code ]:
29211190

Synthetic Route

Precursor & DownStream

Precursor

  • nitromethane
  • N-methyl(methoxymethyl)nitrosamine
  • (Methylimino)bis(formaldehyde)
  • BIS(TRIFLUOROMETHYL)CHLOROPHOSPHINE
  • methylamine
  • Acetyl chloride-d3
  • Diethylamine
  • (E)-methyl 2-chloro-4,4-difluoro-3-hydroxybut-2-enoate
  • N-(triphenylmethyl)methylamine
  • N,N-disilylmethanamine

DownStream

  • N,2,4,6-tetramethylbenzenesulfonamide
  • methylamine
  • Hydrochloric acid
  • 7-chloro-N-methyl-5-phenyl-4H-1,3,4-benzotriazepin-2-amine
  • 3,5,5-trimethyl-2-sulfanylidene-1,3-thiazolidin-4-one
  • 2-ethyl-N-(methylcarbamoylcarbamoyl)butanamide
  • (1-Methyl-1H-Imidazol-5-Yl)Methanol
  • 5-Bromo-N-methylpyrimidin-2-amine
  • Benzamide,N-methyl-3-nitro-
  • 1,1-DIMETHYLUREA

Customs

[ HS Code ]: 2921110090

[ Summary ]:
HS: 2921110090. methylamine, di- or trimethylamine and their salts. VAT:17.0%. tax rebate rate:9.0%. supervision conditions:ab(certificate of inspection for goods inward,certificate of inspection for goods outward). MFN tariff:6.5%. general tariff:30.0%

Articles

Characterization of stress-exposed granulocyte colony stimulating factor using ELISA and hydrogen/deuterium exchange mass spectrometry.

J. Am. Soc. Mass Spectrom. 25(10) , 1747-54, (2014)

Information on the higher-order structure is important in the development of biopharmaceutical drugs. Recently, hydrogen/deuterium exchange coupled with mass spectrometry (HDX-MS) has been widely used...

Methylamine utilization via the N-methylglutamate pathway in Methylobacterium extorquens PA1 involves a novel flow of carbon through C1 assimilation and dissimilation pathways.

J. Bacteriol. 196(23) , 4130-9, (2014)

Methylotrophs grow on reduced single-carbon compounds like methylamine as the sole source of carbon and energy. In Methylobacterium extorquens AM1, the best-studied aerobic methylotroph, a periplasmic...

Quantitative liquid chromatography-electrospray ionization-mass spectrometry analysis of amine-containing metabolites derivatized with cyanuric chloride and methylamine isotopologues.

J. Chromatogr. A. 1388 , 60-8, (2015)

Electrospray ionization (ESI) is the most useful interface for mass spectrometry associated with liquid chromatography (LC). However, analyses of polar metabolites become a challenge because the high ...


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Related Compounds

  • N-methylamine hydrochloride
  • Ethylmethylamine hydrochloride
  • [14C]METHYLAMINE HYDROCHLORIDE
  • [2H3]-Methylamine hydrochloride
  • 2-pyridylmethylamine hydrochloride
  • 2-Thienylmethylamine hydrochloride
  • 3-(Acetyloxy)-5-chloro-2,3-dihydro-7-benzofuransulfonyl chloride
  • 6-(2-chloro-4-fluorophenyl)-2-(methylthio)pyrimidin-4(3H)-one
  • 6-(2-chlorophenyl)-2-(methylthio)pyrimidin-4(3H)-one
  • 6-(2-chloro-6-fluorophenyl)-2-(methylthio)pyrimidin-4(3H)-one
  • 6-(2-chlorobenzyl)-2-(methylthio)pyrimidin-4(3H)-one
  • 6-(4-chlorobenzyl)-2-(methylthio)pyrimidin-4(3H)-one
  • 2-Thiophenesulfonamide, 4-[[hexahydro-4-[5-(trifluoromethyl)-2-pyridinyl]-1H-1,4-diazepin-1-yl]carbonyl]-
  • N-Methyl-3,3-diphenylpropanamine Acetate
  • 6-(2-cyclohexylethyl)-2-(methylthio)pyrimidin-4(3H)-one
  • 6-(2-cyclopentylethyl)-2-(methylthio)pyrimidin-4(3H)-one
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