A
ammonium 5-(2,4,6-trioxoperhydropyrimidin-5-ylideneamino)barbiturate
B
dimethyl amine
Conditions | Yield |
---|---|
at 120℃; |
hydrogenchloride
pyrimidine-2,4,5,6(1H,3H)-tetraone
N-(4-methylphenyl)-5-methyl-1,2-phenylenediamine
ammonium 5-(2,4,6-trioxoperhydropyrimidin-5-ylideneamino)barbiturate
pyrimidine-2,4,5,6(1H,3H)-tetraone
5-methylamino-pyrimidine-2,4,6-trione
ammonium 5-(2,4,6-trioxoperhydropyrimidin-5-ylideneamino)barbiturate
ethanol
ammonia
Alloxantin
ammonium 5-(2,4,6-trioxoperhydropyrimidin-5-ylideneamino)barbiturate
pyrimidine-2,4,5,6(1H,3H)-tetraone
ammonia
water
Alloxantin
ammonium 5-(2,4,6-trioxoperhydropyrimidin-5-ylideneamino)barbiturate
pyrimidine-2,4,5,6(1H,3H)-tetraone
ammonia
uramil
ammonium 5-(2,4,6-trioxoperhydropyrimidin-5-ylideneamino)barbiturate
Conditions | Yield |
---|---|
at 100℃; |
ammonium acetate
water
ammonium 5-(2,4,6-trioxoperhydropyrimidin-5-ylideneamino)barbiturate
Conditions | Yield |
---|---|
at 80℃; |
pyrimidine-2,4,5,6(1H,3H)-tetraone
Alloxantin
ammonium 5-(2,4,6-trioxoperhydropyrimidin-5-ylideneamino)barbiturate
pyrimidine-2,4,5,6(1H,3H)-tetraone
water
Alloxantin
ammonium 5-(2,4,6-trioxoperhydropyrimidin-5-ylideneamino)barbiturate
ammonium acetate
water
Alloxantin
ammonium 5-(2,4,6-trioxoperhydropyrimidin-5-ylideneamino)barbiturate
pyrimidine-2,4,5,6(1H,3H)-tetraone
5-ethylamino-barbituric acid
ammonium 5-(2,4,6-trioxoperhydropyrimidin-5-ylideneamino)barbiturate
Conditions | Yield |
---|---|
at 80℃; |
8-methylxanthine
ammonium 5-(2,4,6-trioxoperhydropyrimidin-5-ylideneamino)barbiturate
pyrimidine-2,4,5,6(1H,3H)-tetraone
ammonium acetate
water
ammonium 5-(2,4,6-trioxoperhydropyrimidin-5-ylideneamino)barbiturate
Conditions | Yield |
---|---|
at 80℃; |
pyrimidine-2,4,5,6(1H,3H)-tetraone
water
ammonium 5-(2,4,6-trioxoperhydropyrimidin-5-ylideneamino)barbiturate
Conditions | Yield |
---|---|
at 80℃; |
Conditions | Yield |
---|---|
at 100℃; |
pyrimidine-2,4,5,6(1H,3H)-tetraone
water
ammonium 5-(2,4,6-trioxoperhydropyrimidin-5-ylideneamino)barbiturate
water
uramil
ammonium 5-(2,4,6-trioxoperhydropyrimidin-5-ylideneamino)barbiturate
water
uramil
ammonium 5-(2,4,6-trioxoperhydropyrimidin-5-ylideneamino)barbiturate
uric Acid
ammonia
nitric acid
A
pyrimidine-2,4,5,6(1H,3H)-tetraone
B
ammonium 5-(2,4,6-trioxoperhydropyrimidin-5-ylideneamino)barbiturate
Conditions | Yield |
---|---|
aufeinanderfolgender Einw.; |
pyrimidine-2,4,5,6(1H,3H)-tetraone
water
glycine
A
ammonium 5-(2,4,6-trioxoperhydropyrimidin-5-ylideneamino)barbiturate
pyrimidine-2,4,5,6(1H,3H)-tetraone
water
rac-Ala-OH
A
ammonium 5-(2,4,6-trioxoperhydropyrimidin-5-ylideneamino)barbiturate
B
acetaldehyde
C
methylammonium carbonate
ammonium acetate
water
Alloxantin
A
ammonium 5-(2,4,6-trioxoperhydropyrimidin-5-ylideneamino)barbiturate
B
uramil
Conditions | Yield |
---|---|
at 80℃; |
Conditions | Yield |
---|---|
With water | |
With potassium hydroxide | |
With sulfuric acid | |
With hydrogen sulfide; water | |
With hydrogenchloride |
The Ammonium purpurate, with the CAS registry number 3051-09-0 and EINECS registry number 221-266-6, has the IUPAC name of Ammonium 2,6-dioxo-5-[(2,4,6-trioxo-5-hexahydropyrimidinylidene)amino]-3H-pyrimidin-4-olate. It is also known as Murexide, and it is the ammonium salt of purpuric acid. It is a kind of reddish purple powder in its dry state, and slightly soluble in water. The molecular formula of this chemical is C8H8O6N6.
Preparation of Ammonium purpurate: It can be prepared by heating alloxantin in ammonia gas to 100°C, or by boiling uramil (5-aminobarbituric acid) with mercury oxide.
Uses of Ammonium purpurate: Its color purpurate ranges from yellow in strong acidic pH through reddish-purple in weakly acidic solutions to blue-purple in alkaline solutions. Because of this property, it is used as in analytical chemistry as a complexometric indicator for complexometric titrations, most often of calcium ions, but also for Cu, Ni, Co, Th and rare earth metals. And it is also used as a colorimetric reagent for measurement of calcium and rare earth metals.
You can still convert the following datas into molecular structure:
(1)SMILES: c1(c([nH]c(=O)[nH]c1=O)[O-])\N=C1\C(NC(=O)NC1=O)=O.[NH4+]
(2)InChI: InChI=1/C8H5N5O6.H3N/c14-3-1(4(15)11-7(18)10-3)9-2-5(16)12-8(19)13-6(2)17;/h(H2,10,11,14,15,18)(H3,12,13,16,17,19);1H3
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