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isothipendyl hydrochloride

Product Name
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
Formula Weight
321.874
MOL File
1225-60-1.mol
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isothipendyl hydrochloride Property

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
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Safety

Toxicity
LD50 oral in rat: 1220mg/kg
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

Precautionary statements

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P270Do not eat, drink or smoke when using this product.

P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.

P330Rinse mouth.

P501Dispose of contents/container to..…

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N-Bromosuccinimide Price

TRC
Product number
I902750
Product name
α-IsothipendylHydrochloride
Packaging
50mg
Price
$175
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
API0025317
Product name
ISOTHIPENDYL HYDROCHLORIDE
Purity
95.00%
Packaging
5MG
Price
$505.44
Updated
2021/12/16
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isothipendyl hydrochloride Chemical Properties,Usage,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

Raw materials

Preparation Products

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isothipendyl hydrochloride Suppliers

Finetech Industry Limited
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027-87465837 19945049750
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China
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Shanghai Chaolan Chemical Technology Center
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QQ:65489617 15618227136
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Finetech Industry Limited
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86 27 87772287
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China
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Wuhan chuang he chemical co. LTD
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15907120073
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Hefei fuya biotechnology co. LTD
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Nanjing Shizhou Biology Technology Co.,Ltd
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TargetMol Chemicals Inc.
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LGC Science (Shanghai) Ltd.
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Xuzhou B&C Chemical Co.,Ltd
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SuZhou GoodChemTech Co., Ltd
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SHANGHAI KEAN TECHNOLOGY CO., LTD.
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Henan Fengda Chemical Co., Ltd
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Shanghai Hao Zhun Biological Technology Co., Ltd.
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View Lastest Price from isothipendyl hydrochloride manufacturers

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

1225-60-1, isothipendyl hydrochlorideRelated 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