| Identification | Back Directory | [Name]
METHAPYRILENE HYDROCHLORIDE | [CAS]
135-23-9 | [Synonyms]
dozar
coryzol
barhist
blueline
capathyn
histafed
methacon
somnicaps
Cohistine
tem-histine
methoxylene
compound01013
METHAPYRILENE HCL
w-53hydrochloride
semikonhydrochloride
thenylenehydrochloride
LABOTEST-BB LT00772145
METHAPYRILENE HYDROCHLORIDE
thenylpyraminehydrochloride
METHAPYRILENE HCL, 1000MG,NEAT
2-dimethylaminoethyl-(2-pyridyl)-(2-thenyl)amine hydrochloride
2-((2-(dimethylamino)ethyl)-2-thenyl-amino)pyridinehydrochloride
2-((2-(dimethylamino)ethyl)-2-thenylamino)-pyridinmonohydrochloride
n,n-dimethyl-n’-(2-pyridyl)-n’-(2-thenyl)ethylenediaminehydrochloride
n,n-dimethyl-n’-(2-pyridyl)-n’-(2-thenyl)-ethylenediaminhydrochloride
n,n-dimethyl-n’-(2-thenyl)-n’-(2-pyridyl-ethylene-diaminehydrochloride)
2-ethanediamine,n,n-dimethyl-n’-2-pyridinyl-n’-(2-thienylmethyl)-monohyd
2-ethanediamine,n,n-dimethyl-n’-2-pyridinyl-n’-(2-thienylmethyl)-monohydro
N,N-DIMETHYL-N'-[2-PYRIDINYL]-N'-[2-THIENYLMETHYL]-1,2-ETHANEDIAMINE HYDROCHLORIDE
N1,N1-DiMethyl-N2-2-pyridinyl-N2-(2-thienylMethyl)-1,2-ethanediaMine Hydrochloride
N,N-DiMethyl-N'-2-pyridinyl-N'-(2-thienylMethyl)-1,2-ethanediaMine MonoHydrochloride
N',N'-dimethyl-N-pyridin-2-yl-N-(thiophen-2-ylmethyl)ethane-1,2-diamine hydrochloride | [EINECS(EC#)]
205-184-8 | [Molecular Formula]
C14H20ClN3S | [MDL Number]
MFCD00050665 | [MOL File]
135-23-9.mol | [Molecular Weight]
297.85 |
| Safety Data | Back Directory | [Hazard Codes ]
T | [Risk Statements ]
25 | [Safety Statements ]
22-36-45 | [RIDADR ]
UN 2811 6.1/PG 3 | [WGK Germany ]
3 | [RTECS ]
UT1750000 | [HazardClass ]
6.1(b) | [PackingGroup ]
III | [Toxicity]
LD50 oral in rat: 200mg/kg |
| Hazard Information | Back Directory | [Originator]
Thenylene ,Abbott,US,1947 | [Uses]
Antihistaminic;Histamine H1 antagonist | [Uses]
Methapyrilene is used as antihistaminic agent. | [Definition]
ChEBI: A hydrochloride that is the monohydrochloride salt of methapyrilene. | [Manufacturing Process]
To a slurry of sodamide in 200 cc of toluene representing 6.7 g of sodium was added at 30° to 40°C, 32.3 g (0.31 mol) of 2-aminopyridine. The mixture was heated to reflux temperature and was refluxed for 1? hours. To the resulting mixture was added over a period of approximately one hour a solution of 32 g of freshly distilled N,N-dimethyl-β-chloroethylamine in 40 to 50 cc of dry toluene, The reaction mixture was then heated for 2 hours at reflux temperature. Thereafter, 200 cc of water was added and the toluene layer was separated and washed with water. The toluene was stripped from the mixture by distillation and the residue was distilled under reduced pressure. The distillate was refractionated and the portion distilled at 93° to 103°C/1 mm was recovered. Yield of N-(2-pyridyl)-N',N'-dimethyl-ethylenediamine, 60%.
A solution of 20 g (0.121 mol) of N-(2-pyridyl)-N',N'-dimethylethylenediamine in 25 cc of toluene was added to a slurry of sodamide in 100 cc of toluene representing 2.8 g of sodium. The mixture was refluxed for one hour. To this mixture was added over a period of ? hour a solution of 16 g (0.121 mol) of 2-thenyl chloride in 25 cc of toluene. The resulting reaction mixture was refluxed for 3 hours. Thereafter, water was added and the toluene layer was separated and washed with water.
The toluene was then stripped off by distillation and the residue was distilled under reduced pressure. The main fraction was redistilled. Yield of N-(2- pyridyl)-N-(2-thenyl)-N',N'-dimethyl-ethylenediamine was 69%; BP 130° to 140°C/0.4 mm. A portion of the product was dissolved in ether and an ether solution of hydrogen chloride was added. The monohydrochloride of N-(2- pyridyl)-N-(2-thenyl)-N',N'-dimethyl-ethylenediamine which separated was washed with ether and dried. | [Therapeutic Function]
Antihistaminic | [General Description]
Methapyrilene hydrochloride,2-[[2-(dimethylamino)-ethyl]-2-thienylarnino]pyridine monohydrochloride (Histadyl) is available as the bitter-tasting, white crystalline powder that is soluble in water(1:0.5), in alcohol (1:5), and in chloroform (1:3). Its solutionshave a pH of about 5.5. It differs structurally from tripelennaminein having a 2-thiophene—methylene group in placeof the benzyl group. The thiophene ring is considered isostericwith the benzene ring, and the isosteres exhibit similaractivity. A study of the solid-state conformation of methapyrilenehydrochloride showed that the trans-conformation is preferredfor the two ethylenediamine nitrogen atoms. The Foodand Drug Administration declared methapyrilene a potentialcarcinogen in 1979, and all products containing it have beenrecalled. | [General Description]
White crystalline powder or solid with a faint odor. Bitter taste. pH (aqueous solution) 5.5. | [Air & Water Reactions]
Water soluble. | [Reactivity Profile]
METHAPYRILENE HYDROCHLORIDE is light sensitive. Solutions of METHAPYRILENE HYDROCHLORIDE in water, DMSO, 95% ethanol or acetone should be stable for 24 hours under normal lab conditions. . Organosulfides are incompatible with acids, diazo and azo compounds, halocarbons, isocyanates, aldehydes, alkali metals, nitrides, hydrides, and other strong reducing agents. Reactions with these materials generate heat and in many cases hydrogen gas. | [Fire Hazard]
Flash point data for METHAPYRILENE HYDROCHLORIDE are not available; however, METHAPYRILENE HYDROCHLORIDE is probably combustible. |
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| Company Name: |
Energy Chemical
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| Tel: |
021-58432009 400-005-6266 |
| Website: |
http://www.energy-chemical.com |
| Company Name: |
ChemeGen 中国
|
| Tel: |
18818260767 |
| Website: |
https://www.chemegen.com |
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