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30125-63-4

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  • 1,3,5-Triazine-2,4-diamine,6-chloro-N2-(1,1-dimethylethyl)-

    Cas No: 30125-63-4

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30125-63-4 Usage

Description

TERBUTHYLAZINE-DESETHYL, also known as a metabolite of the herbicide terbutylazine, is a diamino-1,3,5-triazine with a tert-butyl group at the amino nitrogen and a chloro group at position 6. It is a triazine herbicide used for the control and elimination of weeds.

Uses

Used in Agriculture:
TERBUTHYLAZINE-DESETHYL is used as a herbicide for the control and elimination of weeds in various crops. It helps to protect the crops from the competition of weeds, ensuring better growth and yield.
Used in Environmental Management:
TERBUTHYLAZINE-DESETHYL is used as a tool for environmental management to control the growth of unwanted plants in areas such as roadsides, railways, and other public spaces. This helps to maintain a clean and well-kept appearance in these areas.
Used in Forestry:
TERBUTHYLAZINE-DESETHYL is used in forestry to control the growth of invasive plant species that can negatively impact the health and growth of trees. This helps to maintain the balance of the forest ecosystem and protect valuable timber resources.
Used in Turf Management:
TERBUTHYLAZINE-DESETHYL is used in turf management to control the growth of weeds in lawns, sports fields, and other grassy areas. This helps to maintain a clean and well-kept appearance, as well as improve the overall quality of the turf.
Used in Aquatic Weed Control:
TERBUTHYLAZINE-DESETHYL is used in aquatic weed control to manage the growth of unwanted plants in bodies of water such as lakes, ponds, and reservoirs. This helps to maintain water quality and prevent the spread of invasive plant species.

Check Digit Verification of cas no

The CAS Registry Mumber 30125-63-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,1,2 and 5 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 30125-63:
(7*3)+(6*0)+(5*1)+(4*2)+(3*5)+(2*6)+(1*3)=64
64 % 10 = 4
So 30125-63-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H12ClN5/c1-7(2,3)13-6-11-4(8)10-5(9)12-6/h1-3H3,(H3,9,10,11,12,13)

30125-63-4 Well-known Company Product Price

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  • Sigma-Aldrich

  • (31229)  Terbuthylazin-desethyl  PESTANAL®, analytical standard

  • 30125-63-4

  • 31229-250MG

  • 629.46CNY

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30125-63-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name terbutylazine-desethyl

1.2 Other means of identification

Product number -
Other names Desethylterbuthylazine

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:30125-63-4 SDS

30125-63-4Upstream product

30125-63-4Downstream Products

30125-63-4Relevant articles and documents

Photosensitized degradation of terbuthylazine in water

Sanlaville,Guittonneau,Mansour,Feicht,Meallier,Kettrup

, p. 353 - 362 (2007/10/03)

We investigated the photodegradation of terbuthylazine, an s-triazine herbicide, in the presence of hydrogen peroxide (H2O2), titanium dioxide (TiO2), acetone or humic substances. In the presence of H2O2 and UV light, the degradation of terbuthylazine quickly leads to the formation of ammeline. The degradation pathway consists of dealkylation reactions giving 2-chloro-4,6-diamino-1,3,5-triazine, and then ammeline through hydroxylation. Irradiation of terbuthylazine with simulated solar light in the presence of titanium dioxide gives also dealkylation products in the first stage of degradation. Acetone at 1% (v/v) produces a 7-fold enhancement of the degradation rate. In the presence of humic substances, different results were obtained, depending on the origin of the substances tested. The humic acids isolated from a soil accelerate the degradation speed, whereas the fulvic acids from a small stream reduce it.

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