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1-(4-chlorophenyl)-3-(1-methylpropyl)urea, commonly known as terbutylazine, is a chemical compound belonging to the urea class. It is widely utilized as a herbicide in the agricultural industry, specifically designed to control the growth of broadleaf and grassy weeds. Terbutylazine operates by inhibiting photosynthesis in plants, ultimately leading to their death. Despite its effectiveness, there are concerns regarding its environmental impact and persistence in soil and water, which has resulted in regulatory restrictions in certain regions. It is considered to have low toxicity to mammals when used according to label instructions.

5154-41-6

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5154-41-6 Usage

Uses

Used in Agricultural Industry:
Terbutylazine is used as a herbicide for controlling the growth of broadleaf and grassy weeds in various crops such as corn, soybeans, and sugarcane. Its application helps improve crop yield by reducing competition from weeds and ensuring that the nutrients are directed towards the growth of the desired plants.
The use of terbutylazine in agriculture is aimed at enhancing crop productivity and quality by effectively managing weed populations. However, its environmental impact and persistence in the ecosystem have led to increased scrutiny and regulatory measures in some regions to ensure sustainable agricultural practices.

Check Digit Verification of cas no

The CAS Registry Mumber 5154-41-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,5 and 4 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5154-41:
(6*5)+(5*1)+(4*5)+(3*4)+(2*4)+(1*1)=76
76 % 10 = 6
So 5154-41-6 is a valid CAS Registry Number.

5154-41-6SDS

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-butan-2-yl-3-(4-chlorophenyl)urea

1.2 Other means of identification

Product number -
Other names -

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:5154-41-6 SDS

5154-41-6Downstream Products

5154-41-6Relevant academic research and scientific papers

Leuconostoc mesenteroides glucansucrase synthesis of flavonoid glucosides by acceptor reactions in aqueous-organic solvents

Bertrand, Anne,Morel, Sandrine,Lefoulon, Francois,Rolland, Yves,Monsan, Pierre,Remaud-Simeon, Magali

, p. 855 - 863 (2006)

The enzymatic glucosylation of luteolin was attempted using two glucansucrases: the dextransucrase from Leuconostoc mesenteroides NRRL B-512F and the alternansucrase from L. mesenteroides NRRL B-23192. Reactions were carried out in aqueous-organic solvent

Regioselective O-glycosylation of flavonoids by fungi Beauveria bassiana, Absidia coerulea and Absidia glauca

Sordon, Sandra,Pop?oński, Jaros?aw,Tronina, Tomasz,Huszcza, Ewa

, (2019/02/13)

In the present study, the species: Beauveria bassiana, Absidia coerulea and Absidia glauca were used in biotransformation of flavones (chrysin, apigenin, luteolin, diosmetin) and flavanones (pinocembrin, naringenin, eriodictyol, hesperetin). The Beauveria bassiana AM 278 strain catalyzed the methylglucose attachment reactions to the flavonoid molecule at positions C7 and C3′. The application of the Absidia genus (A. coerulea AM 93, A. glauca AM 177) as the biocatalyst resulted in the formation of glucosides with a sugar molecule present at C7 and C3′ positions of flavonoids skeleton. Nine of obtained products have not been previously reported in the literature.

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