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51857-25-1

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51857-25-1 Usage

Appearance

Yellow crystalline powder

Sensitivity

Low sensitivity to impact and friction

Stability

Highly stable

Detonation velocity

High

Applications

Munitions, military applications, plastic-bonded explosives, insensitive munitions

Environmental impact

Low toxicity and minimal impact on the environment

Check Digit Verification of cas no

The CAS Registry Mumber 51857-25-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,8,5 and 7 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 51857-25:
(7*5)+(6*1)+(5*8)+(4*5)+(3*7)+(2*2)+(1*5)=131
131 % 10 = 1
So 51857-25-1 is a valid CAS Registry Number.
InChI:InChI=1/C14H10N6O9/c1-7-11(17(22)23)3-9(4-12(7)18(24)25)15-16(21)10-5-13(19(26)27)8(2)14(6-10)20(28)29/h3-6H,1-2H3/b16-15-

51857-25-1Downstream Products

51857-25-1Relevant articles and documents

Role of hydroxylamine intermediates in the phytotransformation of 2,4,6-trinitrotoluene by Myriophyllum aquaticum

Wang, Chuanyue,Lyon, Delina Y.,Hughes, Joseph B.,Bennett, George N.

, p. 3595 - 3600 (2007/10/03)

Phytotransformation studies of 2,4,6-trinitrotoluene (TNT) were conducted using Myriophyllum aquaticum to clarify the role of initial intermediates of TNT transformation in the complex product distributions reported previously. 2-Hydroxylamino-4,6-dinitrotoluene (2HA46DNT) and 4-hydroxylamino-2,6-dinitrotoluene (4HA26DNT) were the initial intermediates of TNT phytotransformation. 2HA46DNT and 4HA26DNT were both abiotically transformed to 4,4′,6,6′-tetranitro-2,2′-azoxytoluene (2,2′azoxy) and 2,2′,6,6′-tetranitro-4,4′-azoxytoluene (4,4′azoxy) and also phytoreduced to the related amines 2-amino-4,6-dinitrotoluene (2A46DNT) and 4-amino-2,6-dinitrotoluene (4A26DNT). To further elucidate the initial steps of this TNT phytotransformation pathway, the transformations of known intermediates (including 2HA46DNT, 4HA26DNT, 2A46DNT, 4A26DNT, 2,2′azoxy, and 4,4′azoxy) were monitored in plant systems. The transformation rates were measured, and kinetic analysis using pseudo-first-order models was used to evaluate the relative rates of competing reactions. The formation of the azoxy products was determined to be more rapid than the formation of the amine products. Both the azoxy and amine products were subject to uptake and further transformation by the plant.

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