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isothipendyl hydrochloride

CAS No.
1225-60-1
Chemical Name:
isothipendyl hydrochloride
Synonyms
NSC 169186;Isothipendyl HCl;isothipendyl hydrochloride;α-Isothipendyl Hydrochloride;N,N-dimethyl-1-pyrido[3,2-b][1,4]benzothiazin-10-ylpropan-2-amine hydrochloride;N,N-dimethyl-1-pyrido[3,2-b][1,4]benzothiazin-10-yl-propan-2-amine hydrochloride;dimethyl-(1-methyl-2-pyrido[3,2-b][1,4]benzothiazin-10-yl-ethyl)amine hydrochloride;10H-Pyrido3,2-b1,4benzothiazine-10-ethanamine, N,N,.alpha.-trimethyl-, monohydrochloride;10H-Pyrido[3,2-b][1,4]benzothiazine-10-ethanamine, N,N,a-trimethyl-, monohydrochloride (9CI)
CBNumber:
CB0874889
Molecular Formula:
C16H19N3S.ClH
Molecular Weight:
321.874
MDL Number:
MOL File:
1225-60-1.mol
MSDS File:
SDS
Last updated:2024-03-29 18:52:01

isothipendyl hydrochloride Properties

Melting point 215-220 °C
storage temp. Hygroscopic, Refrigerator, under inert atmosphere
solubility DMSO (Slightly, Heated), Methanol (Slightly)
form Solid
color Yellow to Dark Yellow
Stability Hygrscopic
FDA UNII 953AP1LBV8

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302
Precautionary statements  P264-P270-P301+P312-P330-P501
Toxicity LD50 oral in rat: 1220mg/kg
NFPA 704
0
2 0

isothipendyl hydrochloride price More Price(2)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TRC I902750 α-IsothipendylHydrochloride 1225-60-1 50mg $175 2021-12-16 Buy
American Custom Chemicals Corporation API0025317 ISOTHIPENDYL HYDROCHLORIDE 95.00% 1225-60-1 5MG $505.44 2021-12-16 Buy
Product number Packaging Price Buy
I902750 50mg $175 Buy
API0025317 5MG $505.44 Buy

isothipendyl hydrochloride Chemical Properties,Uses,Production

Originator

Theruhistin,Ayerst,US,1957

Uses

Antihistaminic.

Definition

ChEBI: Isothipendyl hydrochloride is a tertiary amino compound and an aromatic amine.

Manufacturing Process

85 parts of phenylpyridyl amine, 21 parts of powdered sulfur and 1.7 parts of iodine were heated to 275°C for two hours. Evolution of hydrogen sulfide began when the mixture reached a temperature of 250°C and became vigorous when it reached 275°C. Such evolution of hydrogen sulfide diminished after about one hour at 275°C. A light oil was distilled from the reaction mixture under vacuum (pressure = 2-3 mm Hg). This oil which contained phenylpyridyl amine in addition to the thiophenylpyridyl amine was then treated at boiling temperature with approximately the theoretical amount of 2-3 normal HCl until complete solution resulted with formation of the HCl salts of the amines. The solution was then treated with 1 to 2% (based upon the substance mixture) of active carbon and then filtered hot. The nitrate was then cooled to 0°C whereupon the thiophenylpyridyl amine hydrochloride crystallized out while the phenylpyridyl amine hydrochloride remained in solution. The thiophenylpyridyl amine hydrochloride was filtered off and suspended in water and the pH adjusted with half concentrated ammonia to 8. The thiophenylpyridyl amine set free was filtered off and dried. It was in the form of gold yellow needles and had a melting point of 114°C to 115°C.
40 parts of thiophenylpyridyl amine were dissolved in 200 parts of water free toluene. After the addition of 16 parts of soda amide, the mixture was refluxed for 1% hours. Thereafter, 28 parts of dimethylaminoisopropyl chloride in 30 parts of water free toluene were dropped in and the temperature maintained at 20°C to 25°C for 30 minutes. Thereafter, the mixture was heated at 60°C for 30 minutes and subsequently refluxed for 20 minutes. Water and hydrochloride acid were then added to the reaction mixture and this mixture rendered alkaline with NaOH and then the alkalized mixture shaken out with ether. The dimethylaminoisopropyl-N9-thiophenylpyridyl amine base thus obtained was vacuum distilled. It was then converted to hydrochloride salt. The monohydrochloride salt is almost white in color and melts at 213°C to 216°C. The yield was almost 100% of the theoretical.

Therapeutic Function

Antihistaminic

isothipendyl hydrochloride Preparation Products And Raw materials

isothipendyl hydrochloride Suppliers

Global( 18)Suppliers
Supplier Tel Email Country ProdList Advantage
Henan Fengda Chemical Co., Ltd
+86-371-86557731 +86-13613820652 info@fdachem.com China 18225 58
TargetMol Chemicals Inc.
+1-781-999-5354 +1-00000000000 marketing@targetmol.com United States 19892 58
Finetech Industry Limited
+86-27-87465837 +8618971612321 info@finetechnology-ind.com China 9635 58
Alfa Chemistry
+1-5166625404 Info@alfa-chemistry.com United States 21317 58
Finetech Industry Limited 027-87465837 19945049750 sales@finetechnology-ind.com China 9635 58
Nanjing Shizhou Biology Technology Co.,Ltd 025-85560043 15850508050 info@synzest.com China 9287 58
ChemeGen 中国 18818260767 sales@chemegen.com China 6975 58
Nanjing Shizhou Biology Technology Co.,Ltd 18351873721 helen.zhang@synzest.com China 8298 58
Shaanxi DIDU pharmaceutical and Chemical Co., Ltd 15229059051 1027@dideu.com China 9946 58
TargetMol Chemicals Inc. 4008200310 marketing@tsbiochem.com China 24018 58

View Lastest Price from isothipendyl hydrochloride manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
	isothipendyl hydrochloride pictures 2024-03-29 isothipendyl hydrochloride
1225-60-1
US $8.00-1.00 / KG 1KG 99% g-kg-tons, free sample is available Henan Fengda Chemical Co., Ltd

1225-60-1(isothipendyl hydrochloride)Related Search:

isothipendyl hydrochloride 10H-Pyrido3,2-b1,4benzothiazine-10-ethanamine, N,N,.alpha.-trimethyl-, monohydrochloride 10H-Pyrido[3,2-b][1,4]benzothiazine-10-ethanamine, N,N,a-trimethyl-, monohydrochloride (9CI) NSC 169186 dimethyl-(1-methyl-2-pyrido[3,2-b][1,4]benzothiazin-10-yl-ethyl)amine hydrochloride N,N-dimethyl-1-pyrido[3,2-b][1,4]benzothiazin-10-yl-propan-2-amine hydrochloride N,N-dimethyl-1-pyrido[3,2-b][1,4]benzothiazin-10-ylpropan-2-amine hydrochloride Isothipendyl HCl α-Isothipendyl Hydrochloride 1225-60-1