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Imidodicarbonic diamide, also known as N,N,2-trimethyl-, is a chemical compound with the molecular formula C4H10N4O2. It is an organic compound that belongs to the class of imidodicarbonic diamides, which are derivatives of imidodicarbonate. Imidodicarbonic diamide, N,N,2-trimethyl- is characterized by the presence of two amide groups (-CONH2) and a trimethyl group (-N(CH3)2) attached to the imidodicarbonic diamide structure. It is a white crystalline solid and is soluble in water. The compound has potential applications in various fields, including pharmaceuticals and chemical research, due to its unique structure and properties. However, it is essential to handle Imidodicarbonic diamide, N,N,2-trimethyl- with care, as it may have potential health risks and should be used in accordance with proper safety guidelines.

816-00-2

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816-00-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 816-00-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,1 and 6 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 816-00:
(5*8)+(4*1)+(3*6)+(2*0)+(1*0)=62
62 % 10 = 2
So 816-00-2 is a valid CAS Registry Number.

816-00-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-dimethyl-1-(methylcarbamoyl)urea

1.2 Other means of identification

Product number -
Other names Methylamin-N.N-bis-carbonsaeuremethylamid

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:816-00-2 SDS

816-00-2Upstream product

816-00-2Relevant academic research and scientific papers

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 (1986)

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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