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1-(3,4-dimethoxyphenyl)-N-[3-[(3,4-dimethoxyphenyl)methylideneamino]propyl]methanimine, commonly referred to as DMPP, is a chemical compound utilized in the agricultural sector as a nitrification inhibitor. It functions by decelerating the conversion of ammonia to nitrate in the soil, thereby diminishing the risk of nitrogen loss through leaching and denitrification. DMPP is significant for sustainable agriculture as it enhances the efficiency of nitrogen fertilizers and mitigates environmental pollution. Moreover, it has been demonstrated to possess low toxicity and minimal impact on soil microorganisms, making it a valuable asset for optimizing nutrient management in crop production.

5767-54-4

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5767-54-4 Usage

Uses

Used in Agricultural Practices:
1-(3,4-dimethoxyphenyl)-N-[3-[(3,4-dimethoxyphenyl)methylideneamino]propyl]methanimine is used as a nitrification inhibitor for the following reasons:
It slows down the conversion of ammonia to nitrate in the soil, reducing nitrogen losses through leaching and denitrification.
It improves the efficiency of nitrogen fertilizers, leading to better crop yields and reduced environmental pollution.
It has low toxicity and minimal impact on soil microorganisms, promoting a healthy soil ecosystem.

Check Digit Verification of cas no

The CAS Registry Mumber 5767-54-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,6 and 7 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5767-54:
(6*5)+(5*7)+(4*6)+(3*7)+(2*5)+(1*4)=124
124 % 10 = 4
So 5767-54-4 is a valid CAS Registry Number.

5767-54-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3,4-dimethoxyphenyl)-N-[3-[(3,4-dimethoxyphenyl)methylideneamino]propyl]methanimine

1.2 Other means of identification

Product number -
Other names N,N'-bis-(3,4-dimethoxybenzylidene)-1,3-diaminopropane

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:5767-54-4 SDS

5767-54-4Relevant academic research and scientific papers

Catalytic activity of Ru/tetrahydropyrimidinium salts system for transfer hydrogenation reactions

Karaca, Emine ?zge,Gürbüz, Nevin,Arslan, Hakan,Vanderveer, Don,?zdemir, Ismail

, p. 475 - 480 (2015)

New 1,3-dialkyltetrahydropyrimidinium salts as NHC precursors have been synthesized and characterized. The in situ prepared three-component 1,3-dialkyltetrahydropyrimidinium salts/[RuCl2(p-cymene)]2 and KOH catalyzes quantitatively t

SYNTHESIS OF N,N'-DIARALKYL-2H-1,2,6-TETRAHYDROTHIADIAZINES

Meisenheimer, John L.,Meisenheimer, John L.,Raya, Diana G.,Stapleton, Michael C.,Goddard, Carl J.

, p. 2229 - 2236 (2007/10/02)

Several derivatives of the 2H-1,2,6-tetrahydrothiadiazine ring system have been synthesized by the interaction of the sulfur transfer reagent N,N-thiobisphthalimide (TBP) with appopriately substituted N,N'-bis-(benzyl)-1,3-diaminopropanes.

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