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18305-11-8

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18305-11-8 Usage

Description

1-(2-chlorophenyl)-6,6-dimethyl-1,6-dihydro-1,3,5-triazine-2,4-diamine, commonly known as Terbutryn, is a synthetic herbicide that belongs to the triazine chemical class. It is specifically designed to control broadleaf and grassy weeds in various settings, including agricultural fields and non-crop areas. Terbutryn operates by inhibiting the photosynthesis process in plants, which leads to cell membrane damage and ultimately results in plant death. As a moderately hazardous chemical according to the World Health Organization, it is crucial to handle and apply Terbutryn with care to minimize its environmental impact on non-target organisms such as aquatic species.

Uses

Used in Agricultural Applications:
Terbutryn is used as a herbicidal agent for controlling broadleaf and grassy weeds in agricultural fields. Its application reason is to enhance crop yield by reducing competition from weeds, which can negatively affect the growth and productivity of desired crops.
Used in Non-Crop Areas:
In non-crop areas, Terbutryn is used as a herbicide to manage weed growth, maintaining the aesthetic and functional aspects of landscapes, gardens, and other such areas. The application reason is to prevent the overgrowth of unwanted vegetation that can lead to various ecological and maintenance issues.
Environmental Considerations:
Given its persistence in the environment and potential risks to non-target organisms, Terbutryn is categorized as a moderately hazardous chemical by the World Health Organization. Therefore, it is essential to follow proper safety guidelines and application techniques to minimize its environmental impact. This includes using the chemical judiciously, adhering to recommended dosages, and considering alternative weed management strategies when appropriate.

Check Digit Verification of cas no

The CAS Registry Mumber 18305-11-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,3,0 and 5 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 18305-11:
(7*1)+(6*8)+(5*3)+(4*0)+(3*5)+(2*1)+(1*1)=88
88 % 10 = 8
So 18305-11-8 is a valid CAS Registry Number.

18305-11-8SDS

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 1-(2-chlorophenyl)-6,6-dimethyl-1,3,5-triazine-2,4-diamine,hydrochloride

1.2 Other means of identification

Product number -
Other names 1-(2-Chlor-phenyl)-6,6-dimethyl-1,6-dihydro-[1,3,5]triazin-2,4-diyldiamin,Hydrochlorid

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:18305-11-8 SDS

18305-11-8Relevant articles and documents

Synthesis and in vitro evaluation of 2,4-diamino-1,3,5-triazine derivatives as neuronal voltage-gated sodium channel blockers

Ma, Xiang,Poon, Thong-Yuen,Wong, Peter Tsun Hon,Chui, Wai-Keung

supporting information; experimental part, p. 5644 - 5647 (2010/04/26)

Neuronal sodium channels blockers interfere with ion flux and have been used for managing neuropathic pain, epilepsy, and cerebral ischemic disorders. In the current study, four groups of 2,4-diamino-1,3,5-triazine derivatives were synthesized and investigated for their neuronal sodium channels binding activity. 5-Aryl-1,3,5-triazaspiro[5.5]undeca-1,3-diene-2,4-diamines (4a-4j) were found to have the best neuronal sodium binding activity among the four groups of triazines evaluated. Derivatives 4a-4j blocked the sodium channels with IC50 values ranged from 4.0 to 14.7 μM. The result from this study showed that analogues of 2,4-diamino-1,3,5-triazines could be used as leads for the discovery of neuronal sodium channels blockers for managing central nervous system related disorders.

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