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1446-17-9

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1446-17-9 Usage

Safety Profile

Human poison by ingestion.Human systemic effects by ingestion: muscle weakness. Ahuman teratogen. Human reproductive effects:termination of pregnancy; developmental abnormalities ofthe eye, ear, and musculoskeletal system; and effects onnewborn and p

Check Digit Verification of cas no

The CAS Registry Mumber 1446-17-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,4 and 6 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1446-17:
(6*1)+(5*4)+(4*4)+(3*6)+(2*1)+(1*7)=69
69 % 10 = 9
So 1446-17-9 is a valid CAS Registry Number.
InChI:InChI=1/C18H26ClN3.H3O4P/c1-4-22(5-2)12-6-7-14(3)21-17-10-11-20-18-13-15(19)8-9-16(17)18;1-5(2,3)4/h8-11,13-14H,4-7,12H2,1-3H3,(H,20,21);(H3,1,2,3,4)

1446-17-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-N-(7-chloroquinolin-4-yl)-1-N,1-N-diethylpentane-1,4-diamine,phosphoric acid

1.2 Other means of identification

Product number -
Other names chloroquinone phosphate

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:1446-17-9 SDS

1446-17-9Upstream product

1446-17-9Downstream Products

1446-17-9Relevant articles and documents

Preparation method of chloroquine phosphate

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Paragraph 0030; 0037-0038; 0039; 0046-0047; 0048; 0055-0056, (2021/05/26)

The invention discloses a preparation method of chloroquine phosphate, namely 7-chloro-4-(4-diethylamino-1-methylbutylamino)quinoline diphosphate. The preparation method comprises the following steps: (1) carrying out a condensation reaction on 4,7-dichloroquinoline and 2-amino-5-diethylaminopentane, and carrying out alkalization extraction, concentration and crystallization to obtain chloroquine; and (2) salifying the chloroquine obtained in the step (1) and phosphoric acid to obtain chloroquine phosphate. The method avoids the use of phenol, is simple in reaction, and is beneficial to industrial production; and the chloroquine is crystallized to improve the purity and then salified with the phosphoric acid, so product appearance is good, the purity of the produced chloroquine phosphate is greater than or equal to 99.5%, and a single impurity is less than 0.1% (according to an HPLC area normalization method).

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