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2,5 Diamino 4,6 Dihydroxy Pyrimidine hydrocholoride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

60337-65-7

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60337-65-7 Usage

Function

Inhibitor of the enzyme dopa decarboxylase

Use

Treatment of neurological disorders such as Parkinson's disease and restless leg syndrome

Potential antitumor effects

Inhibits growth of certain cancer cells

Form

Hydrochloride salt

Mode of administration

Pharmaceutical drug

Check Digit Verification of cas no

The CAS Registry Mumber 60337-65-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,3,3 and 7 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 60337-65:
(7*6)+(6*0)+(5*3)+(4*3)+(3*7)+(2*6)+(1*5)=107
107 % 10 = 7
So 60337-65-7 is a valid CAS Registry Number.

60337-65-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name isouramil

1.2 Other means of identification

Product number -
Other names 2,6-Diamino-5-hydroxy-3H-pyrimidin-4-one

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:60337-65-7 SDS

60337-65-7Downstream Products

60337-65-7Relevant academic research and scientific papers

Determination and stability of divicine and isouramil produced by enzymatic hydrolysis of vicine and convicine of faba bean

Pulkkinen, Marjo,Zhou, Xiao,Lampi, Anna-Maija,Piironen, Vieno

, p. 10 - 19 (2016/06/13)

The aglycones of vicine and convicine, divicine and isouramil, are the causative agents of favism and, therefore, should be analysed along with vicine and convicine in research seeking to eliminate them. This study investigated the stability of the aglycones produced by hydrolysis with β-glucosidase. Reversed-phase, high-performance liquid chromatography (HPLC) with UV detection was shown to be able to observe both aglycone formation and further reactions in isolated fractions and extract made from faba bean and in faba bean suspension. Divicine and isouramil were unstable and degraded almost completely in extract in 60 min and completely in fractions in 120 min at a pH of 5 at 37 °C. Adding sodium ascorbate delayed degradation of divicine. Divicine was more stable at 20 °C than at 37 °C. Being able to show formation and degradation of the aglycones, the proposed method allows monitoring of the vicine and convicine detoxification process.

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