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chlorazine

chlorazine Structure
CAS No.
580-48-3
Chemical Name:
chlorazine
Synonyms
G25804;chlorazine;S-TRIAZINE,2-CHLORO-4,6-BIS(DIETHYLAMINO)-;2,4-Di-(N,N'-Diethylamino)-6-Chlorotriazine;2,4-DI-(N,N'-DIETHYLAMINO)-6-CHLOROTRIAZINE;2,4-bis(N,N-diethylamino)-6-chloro-1,3,5-triazine;[4-chloro-6-(diethylamino)-s-triazin-2-yl]-diethyl-amine;6-chloro-N2,N2,N4,N4-tetraethyl-1,3,5-triazine-2,4-diamine;1,3,5-Triazine-2,4-diamine, 6-chloro-N2,N2,N4,N4-tetraethyl-;6-chloro-2-N,2-N,4-N,4-N-tetraethyl-1,3,5-triazine-2,4-diamine
CBNumber:
CB4126737
Molecular Formula:
C11H20ClN5
Molecular Weight:
257.76
MOL File:
580-48-3.mol
MSDS File:
SDS
Modify Date:
2023/11/27 15:17:06

chlorazine Properties

Melting point 27°C
Boiling point 404.64°C (rough estimate)
Density 1.0956
refractive index 1.5320 (estimate)
pka 3.18±0.10(Predicted)
Water Solubility 10mg/L(21 ºC)
EPA Substance Registry System Chlorazine (580-48-3)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P280-P301+P312-P302+P352-P305+P351+P338
Risk Statements  36/37/38
Safety Statements  26-36/37/39

chlorazine Chemical Properties,Uses,Production

Description

Chlorazine is a drug that belongs to the class of phenothiazines. It is used in the treatment of nausea and vomiting, as well as for sedation before surgery or endoscopy, but it also has some undesirable side effects. Chlorazine can be detected by chromatographic analysis and is biocompatible with polymer matrices. The drug has been shown to inhibit the growth of cells (in-vitro) by binding to cell nuclei. The chlorazine molecule has been found to have significant upregulation on α7 nicotinic acetylcholine receptors and pharmacological agents such as receptor activity. This drug may also have a matrix effect on chemical inhibitors.

Chemical Properties

Solid. Soluble in hydrocarbons, alcohols, ketones; insoluble in water.

Uses

Herbicide.

Preparation

Chlorazine is formed through a reaction between cyanuric chloride and diethylamine.

Mode of action

Their chief mode of action appears to involve carbohydrate metabolism. The chlorinated s-triazines inhibit starch accumulation by blocking the production of sugars. Similar behavior has been shown for the methoxy & methylthio-s-triazines. It has been reported that the s-triazines affect the tricarboxylic acid cycle with activation of phospho-phenyl pyruvate-carboxylase causing the disappearance of sucrose & glyceric acid with the formation of aspartic & malic acids.

chlorazine Preparation Products And Raw materials

Raw materials

Preparation Products

chlorazine Suppliers

Global( 24)Suppliers
Supplier Tel Country ProdList Advantage Inquiry
CONIER CHEM AND PHARMA LIMITED +8618523575427 China 49403 58 Inquiry
Shaanxi Dideu Medichem Co. Ltd +86-29-87569266 15319487004 China 4088 58 Inquiry
Aladdin Scientific +1-+1(833)-552-7181 United States 52927 58 Inquiry
ABCR GmbH & CO. KG 49 721 95061 0 Germany 6846 75 Inquiry
Beijing Jin Ming Biotechnology Co., Ltd. 010-60605840 15801484223; China 29778 58 Inquiry
Shaanxi DIDU pharmaceutical and Chemical Co., Ltd 15229059051 China 9978 58 Inquiry
Bide Pharmatech Ltd. 400-6005915 China 39668 58 Inquiry
Shandong Hydrocarbon Bio-Chemical Co. LTD 17860268208 China 938 58 Inquiry
Jinan Tai Hang Seng Material Technology Co., LTD 17852565707 China 14 58 Inquiry
Beijing Solarbio Science & Tecnology Co., Ltd. 010-50973130 17801761073 China 50471 58 Inquiry
G25804 2,4-DI-(N,N'-DIETHYLAMINO)-6-CHLOROTRIAZINE S-TRIAZINE,2-CHLORO-4,6-BIS(DIETHYLAMINO)- 2,4-bis(N,N-diethylamino)-6-chloro-1,3,5-triazine [4-chloro-6-(diethylamino)-s-triazin-2-yl]-diethyl-amine 6-chloro-2-N,2-N,4-N,4-N-tetraethyl-1,3,5-triazine-2,4-diamine 6-chloro-N2,N2,N4,N4-tetraethyl-1,3,5-triazine-2,4-diamine chlorazine 1,3,5-Triazine-2,4-diamine, 6-chloro-N2,N2,N4,N4-tetraethyl- 2,4-Di-(N,N'-Diethylamino)-6-Chlorotriazine 580-48-3 C11H20ClN5