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5-23-11-00075 (Beilstein Handbook Reference)

5-23-11-00075 (Beilstein Handbook Reference) Suppliers list
Company Name: BOC Sciences
Tel: 16314854226; +8616314854226
Email: inquiry@bocsci.com
Products Intro: Product Name:CREDAZINE
CAS:14491-59-9
Purity:98% Remarks:Please reach out to us for more information about custom solutions.
Company Name: TargetMol Chemicals Inc.
Tel: +1-781-999-5354;
Email: support@targetmol.com
Products Intro: Product Name:Credazine;H-722;SW-670;NIA 20439;Kusakira;BRN 0880257
CAS:14491-59-9
Package:100 mg;500 mg Remarks:REAGENT;FOR LABORATORY USE ONLY
Company Name: Shanghai Jiegu Biotechnology Co., Ltd.  
Tel: 021-51698675
Email: sales@jiejiegroup.com
Products Intro: Product Name:5-23-11-00075 (Beilstein Handbook Reference)
CAS:14491-59-9
Purity:97% HPLC Package:100KG;1KG
Company Name: TargetMol Chemicals Inc.  
Tel: 15002134094
Email: marketing@targetmol.cn
Products Intro: Product Name:Credazine
CAS:14491-59-9
Package:25mg/RMB 10600
Company Name: BOC Sciences  
Tel: 16314854226
Email: info@bocsci.com
Products Intro: Product Name:CREDAZINE
CAS:14491-59-9
Purity:98%
5-23-11-00075 (Beilstein Handbook Reference) Basic information
Product Name:5-23-11-00075 (Beilstein Handbook Reference)
Synonyms:5-23-11-00075 (Beilstein Handbook Reference);3-(2-methylphenoxy)pyridazine;Credazin;H-722;Kusakira;NIA 20439;SW-6701;Pyridazine, 3-(2-methylphenoxy)-
CAS:14491-59-9
MF:C11H10N2O
MW:186.21
EINECS:
Product Categories:
Mol File:14491-59-9.mol
5-23-11-00075 (Beilstein Handbook Reference) Structure
5-23-11-00075 (Beilstein Handbook Reference) Chemical Properties
Melting point 78°C
Boiling point 320.7°C (rough estimate)
density 1.1458 (rough estimate)
refractive index 1.5300 (estimate)
Water Solubility 1.996g/L(temperature not stated)
EPA Substance Registry SystemPyridazine, 3-(2-methylphenoxy)- (14491-59-9)
Safety Information
MSDS Information
5-23-11-00075 (Beilstein Handbook Reference) Usage And Synthesis
DescriptionCredazine is an obsolete herbicide that was used to control grasses and broadleaved weeds. The substance has not been extensively studied and so little information is known regarding its environmental fate, ecotoxicity or impact on human health.
Production MethodsCredazine was produced using the same multipurpose agrochemical manufacturing methods applied to other chloro s triazines of the 1960s–1980s. Commercial production began with cyanuric chloride, the universal starting material for this herbicide class, which was reacted stepwise with the appropriate alkylamines or substituted amines under controlled temperature conditions to ensure selective mono and di substitution on the triazine ring. Each substitution step required careful cooling, pH control, and staged addition because cyanuric chloride reacts exothermically and its reactivity decreases sharply with each substitution. After the final amine was introduced to form credazine’s specific dialkylamino triazine structure, the reaction mixture was neutralised, filtered, and subjected to solvent exchange and crystallisation to yield technical grade material.
DefinitionChEBI: Credazine is an aromatic ether.
Mechanism of actionProtease biosynthesis inhibition, inhibits plant division
Pesticide TypeHerbicide
5-23-11-00075 (Beilstein Handbook Reference) Preparation Products And Raw materials
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