550-70-9 Usage
Description
TRIPROLIDINE HYDROCHLORIDE is a hydrochloride resulting from the formal reaction of equimolar amounts of triprolidine and hydrogen chloride. It is a histamine H1 receptor antagonist with antihistaminic and anticholinergic properties, making it a versatile pharmaceutical compound for various applications.
Uses
Used in Pharmaceutical Industry:
TRIPROLIDINE HYDROCHLORIDE is used as an antihistaminic agent for the treatment and prevention of symptoms associated with allergies. It is particularly effective in providing relief for conditions such as urticaria, rhinitis, and various pruritic skin disorders.
TRIPROLIDINE HYDROCHLORIDE is used as a histamine H1 receptor antagonist for the prevention and treatment of chronic muscle pain.
Additionally, TRIPROLIDINE HYDROCHLORIDE is used in combination with cold medicine to provide relief for flu-like symptoms, thanks to its anticholinergic properties.
Therapeutic Function
Antihistaminic
Check Digit Verification of cas no
The CAS Registry Mumber 550-70-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,5 and 0 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 550-70:
(5*5)+(4*5)+(3*0)+(2*7)+(1*0)=59
59 % 10 = 9
So 550-70-9 is a valid CAS Registry Number.
InChI:InChI=1/C19H22N2.ClH/c1-16-7-9-17(10-8-16)18(19-6-2-3-12-20-19)11-15-21-13-4-5-14-21;/h2-3,6-12H,4-5,13-15H2,1H3;1H/b18-11+;
550-70-9Relevant articles and documents
A PROCESS FOR PREPARATION OF E-ISOMER OF 1-(4-METHYLPHENYL)- 1-(2-PYRID YL)-3-PYRROLIDINO PROP-1-ENE AND ACID ADDITION SALTS THEREOF
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Page/Page column 11-12, (2009/08/14)
A process for preparation of E-isomer of 1-(4-methylphenyl)-1-(2-pyridyl)-3- pyrrolidinoprop-1-ene of Formula-I, and acid addition salts thereof, said process comprising; dehydrating 1-(4-methylphenyl)-l -(2-pyridyl)-3-pyrrolidinopropan-1-ol of Formula III followed by adding a base solution to obtain a mixture of E and Z isomers of 1-(4-methylphenyl)-1-(2-pyridyl)-3-pyrrolidinoprop-1-ene, and washing said mixture of E and Z isomers of 1-(4-methylphenyl)-1-(2-pyridyl)-3- pyrrolidinoprop-1-ene with water to dissolve Z isomer and to obtain E-isomer of 1- (4-methylphenyl)-1-(2-pyridyl)-3-pyrrolidinoprop-1-ene of Formula I, which is substantially free from Z isomer.