29091-05-2

Basic information

• Product Name: Dinitramine
• Synonyms: 1,3-benzenediamine,n(sup3),n(sup3)-diethyl-2,4-dinitro-6-(trifluoromethyl);5-dinitro-;cobeko;cobexo;dinitroamine;ifluoro-;n(1),n(1)-diethyl-2,6-dinitro-4-trifluoromethyl-m-phenylenediamine;n(3),n(3)-diethyl-2,4-dinitro-6-(trifluoromethyl)-1,3-benzenediamine
• CAS NO: 29091-05-2
• Molecular Formula: C₁₁H₁₃F₃N₄O₄
• Molecular Weight: 322.24
• EINECS: 249-419-2
• Product Categories: 3-Diethylamino-2,4-dinitro-6-trifluoromethylaniline
• Mol File: 29091-05-2.mol
• Article Data: 5

Chemical Properties

• Melting Point: 98-99°C
• Boiling Point: 409.1°Cat760mmHg
• Flash Point: 201.2°C
• Appearance: /
• Density: 1.4291 (estimate)
• Refractive Index: 1.5700 (estimate)
• PKA: -0.39±0.50(Predicted)
• Water Solubility: 1.1mg/L(25 oC)
• BRN: 2822138
• CAS DataBase Reference: Dinitramine(CAS DataBase Reference)
• NIST Chemistry Reference: Dinitramine(29091-05-2)
• EPA Substance Registry System: Dinitramine(29091-05-2)

Safety Data

• Hazard Codes: Xn;N,N,Xn
• Statements: 21-50/53
• Safety Statements: 36/37-60-61
• RIDADR: UN 3077
• WGK Germany: 3
• RTECS: XS9990000
• Hazardous Substances Data: 29091-05-2(Hazardous Substances Data)

Usage

Uses

Dinitramine, is a herbicide that has been used particularly n soybean fields

Upstream product

• 36438-51-4 2-Chloro-4-diethylamino-3,5-dinitrotrifluoromethylbenzene 

Relevant articles and documents

Synthesis and evaluation of oryzalin analogs against Toxoplasma gondii

The synthesis and evaluation of 20 dinitroanilines and related compounds against the obligate intracellular parasite Toxoplasma gondii is reported. Using in vitro cultures of parasites in human fibroblasts, we determined that most of these compounds selectively disrupted Toxoplasma microtubules, and several displayed sub-micromolar potency against the parasite. The most potent compound was N1,N1-dipropyl-2,6-dinitro-4-(trifluoromethyl)-1,3- benzenediamine (18b), which displayed an IC50 value of 36 nM against intracellular T. gondii. Based on these data and another recent report [Ma, C.; Tran, J.; Gu, F.; Ochoa, R.; Li, C.; Sept, D.; Werbovetz, K.; Morrissette, N. Antimicrob. Agents Chemother. 2010, 54, 1453], an antimitotic structure-activity relationship for dinitroanilines versus Toxoplasma is presented.

Pesticide-polymer systems prepared from vinyl monomers

Controlled release pesticide-polymer systems are prepared by the polymerization of vinyl monomers containing pendant pesticides. The vinyl monomers are prepared by reacting an acrylic acid derivative with a pesticide or a pesticide derivative having an active hydrogen. The pesticide-polymer systems prepared from the pesticide vinyl monomers release the active pesticide material by hydrolysis or chemical depolymerization under conditions of use.

Dinitroaniline purification with bromine and chlorine

The present invention is directed to a process for the removal of nitrosamines from dinitroanilines.