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908844-46-2

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908844-46-2 Usage

Chemical Properties

Yellow Powder

Uses

Different sources of media describe the Uses of 908844-46-2 differently. You can refer to the following data:
1. A metabolite of Quinacrine, an antimalarial compound
2. A metabolite of Quinacrine, an antimalarial compound.

Check Digit Verification of cas no

The CAS Registry Mumber 908844-46-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,8,8,4 and 4 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 908844-46:
(8*9)+(7*0)+(6*8)+(5*8)+(4*4)+(3*4)+(2*4)+(1*6)=202
202 % 10 = 2
So 908844-46-2 is a valid CAS Registry Number.

908844-46-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name Monodesethyl Quinacrine, Dihydrochloride

1.2 Other means of identification

Product number -
Other names 4-N-(6-chloro-2-methoxyacridin-9-yl)-1-N-ethylpentane-1,4-diamine

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:908844-46-2 SDS

908844-46-2Upstream product

908844-46-2Downstream Products

908844-46-2Relevant articles and documents

Determination of quinacrine dihydrochloride dihydrate stability and characterization of its degradants

Rotival, Romain,Espeau, Philippe,Corvis, Yohann,Guyon, Francois,Do, Bernard

experimental part, p. 3223 - 3232 (2012/06/15)

Although quinacrine dihydrochloride dihydrate is a widely used drug substance, a comprehensive determination of its stability profile is lacking. In this work, an integrative approach is implemented to determine the drug stability both in the solid state and aqueous solutions, identify the impurities that can be found in the active pharmaceutical ingredient, and evaluate the associated toxicity risks. Thermal analyses pointed out a two-step dehydration of the solid state. This phenomenon seems to be consistent with the organization of the water molecules in the crystal structure and results in the destruction of the lattice. Seven related compounds of quinacrine have been identified by liquid chromatography-ion trap mass spectrometry. The main thermal degradant both in the solid state and the solution corresponds to the N-deethyl compound, whereas quinacrine tertiary amine oxyde appears to be a signal impurity of oxidative stress in solution. Moreover, two photolytic impurities can be formed in solution either by aromatic amine cleavage or via O-demethylation. Additionally, using computational approaches, the analysis of the potential toxicity of the impurities compared with the parent compound one shows that ketone and O-demethyl derivatives may exhibit specific toxicity profiles.

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