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1,3,5-trimethyl-1,3,5-triazinane-2,4-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

41221-01-6

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41221-01-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41221-01-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,2,2 and 1 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 41221-01:
(7*4)+(6*1)+(5*2)+(4*2)+(3*1)+(2*0)+(1*1)=56
56 % 10 = 6
So 41221-01-6 is a valid CAS Registry Number.

41221-01-6Downstream Products

41221-01-6Relevant academic research and scientific papers

Studies of Reactions of 1,3,5-Trimethylbiuret and 1,3-Dimethylurea with Chloroform

D'Silva, Themistocles D. J.,Lopes, Anibal

, p. 795 - 796 (1986)

1,3,5-Trimethylbiuret and 1,3-dimethylurea react with chloroform at temperatures above 200 deg C to produce 1,3,5-trimethyl-1,3,5-triazinane-2,4-dione (4), 1,3-dimethyl-1,3,5-triazinane-2,4,6-trione (5), and 1,3,5-trimethyl-1,3,5-triazinane-2,4,6-trione (3), besides minor quantities of other by-products, via trimerization reactions involving MIC, isocyanic acid, and N-methylenemethylamine.

Studies of Methyl Isocyanate Chemistry in the Bhopal Incident

D'Silva, Themistocles D. J.,Lopes, Anibal,Jones, Russell L.,Singhawangcha, Sureerat,Chan, John K.

, p. 3781 - 3788 (2007/10/02)

Following the methyl isocyanate leak from Tank 610 at the Bhopal plant, the residual material from the tank was analyzed for its contents.Approximately 70percent of the residue was comprised of three cyclic materials: 1,3,5-trimethyl-1,3,5-triazine-2,4,6(1H,3H,5H)-trione or methyl isocyanate trimer (5), 1,3-dimethyl-1,3,5-triazine-2,4,6(1H,3H,5H)-trione or dimethyl isocyanurate (6), and dihydro-1,3,5-trimethyl-1,3,5-triazine-2,4-(1H,3H)-dione or dihydrotrimethyltriazinedione (7).Minor quantities of methyl-substituted ureas, biurets, and amine hydrochlorides were also found.The composition of the residue was replicated very closely by the products obtained when a mixture of methyl isocyanate (84.4percent), chloroform (12.0percent), and water (3.6percent) was heated at 225 deg C under pressure in a stainless steel reactor.Experimental results are consistent with the view that under these conditions methyl isocyanate reacts initially with water to form 1,3-dimethylurea (1) and 1,3,5-trimethylbiuret (2).At temperatures between 100 deg C and 225 deg C these products decompose to reactive intermediates which further react exothermically to form the aforementioned cyclic materials, trimethylurea, and mono-, di-, and trimethylamine hydrochlorides.The decomposition of 1 and 2 is facilitated by the presence of chloroform and metals.Other experiments involving 13C-enriched chloroform have given support to the proposed mechanisms for formation of 6 and 7.

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