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Autres produits en vente chaude (Poudre brute)

» Autres produits en vente chaude (Poudre brute)

99% Puriy Pramipexole for Parkinson Syndrome White Powder

CATÉGORIE ET ​​ÉTIQUETTES:
Autres produits en vente chaude (Poudre brute)
Attestation: ISO9001, GV,UKAS
Numéro de modèle: 191217-81-9
Quantité minimum d'achat: Free sample available
Heure de livraison: 3-6 jours de travail
Modalités de paiement: T/T, Western union, MoneyGram, Bitcoins
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  • Caractéristiques

99% Puriy Pramipexole for Parkinson Syndrome White Powder

 

Détail rapide

 


N ° CAS.: 191217-81-9
Synonymes: (S)-2-Amino-4,5,6,7-tetrahydro-6-(propylamino)benzothiazole Dihydrochloride Monohydrate; Pramipexole dihydrochloride; Pramipexole dihydroch;
(S)-2-amino-4,5,6,7-tetrahydro-6-(propylamino)benzothiazole dihydrochloride PPX dihydrochloride; Pramipexole; Pramipexole 2HCl Monohydrate;Pramipexole Dihydrochloride Monohydrate;
Formule: C10H21Cl2N3OS
Exact Mass: 301.07800
Masse moléculaire: 302.26400
Apparence : poudre cristalline blanche à blanc cassé
Point d'ébullition: 378°C à 760 mmHg
Point de rupture: 182.4C
Vapor Pressure: 9.93E-11mmHg at 25°C
PSA: 88.41000
LogP: 4.09400

 

La description

 

Pramipexole dihydrochloride monohydrate is used for treatment of idiopathic Parkinson’s disease. During routine monitoring of the drug samples by HPLC, two impurities of pramipexole were observed. The molecular weights of the impurities were determined by LC-MS. The structures were postulated to be (6S)-(-)-2-amino-6-ethylamino-4,5,6,7-tetrahydrobenzo thiazole (ethyl pramipexole) et (6S)-(-)-2,6-di-(n-propylamino)-4,5,6,7- tetrahydrobenzothiazole (dipropyl pramipexole). These were synthesized subsequently, and characterized by NMR and IR. Their presence was confirmed by spiking into pramipexole sample and carrying out HPLC analysis. To our knowledge, ethyl pramipexole and dipropyl pramipexole have not been reported as process impurities elsewhere.

 

Bipolar Depression:

In a single controlled study of twenty one patients, pramipexole was found to be highly effective in the treatment of bipolar depression. Treatment was initiated at 0.125 mg three times a day and increased at a rate of 0.125 mg three times a day to a limit of 4.5 mg daily until the patientscondition satisfactorily responded to the medication or they could not abide the side effects. The final average dosage was 1.7 ± 0.9 mg daily. The incidence of hypomania in the treatment group was no greater than in the control group, although the size of the study is too small to determine risks for manic switch.

 

 

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