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VIOLURIC ACID

Product Name
VIOLURIC ACID
CAS No.
87-39-8
Chemical Name
VIOLURIC ACID
Synonyms
VLA;5-(Hydroxyimino)pyrimidine-2,4,6(1H,3H,5H)-trione;NSC 56338;VIOLURIC ACID;ALLOXAN-5-OXIME;Violuric Acid Violuric acid hydrate,95%;5-ISONITROSOBARBITURIC ACID;5-HYDROXYIMINOBARBITURIC ACID;87-39-8 C4H3N3O4 VIOLURIC ACID
CBNumber
CB0477879
Molecular Formula
C4H3N3O4
Formula Weight
157.08
MOL File
87-39-8.mol
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VIOLURIC ACID Property

Melting point:
240-250 °C (dec.)
Boiling point:
281.7°C (rough estimate)
Density 
1.8278 (rough estimate)
vapor pressure 
0Pa at 25℃
refractive index 
1.5000 (estimate)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
solubility 
Aqueous Acid (Sparingly), DMSO (Sparingly), Methanol (Slightly)
pka
4.7(at 25℃)
form 
Solid
color 
Off-White
Water Solubility 
7.04g/L at 20℃
Merck 
10000
Stability:
Hygroscopic
LogP
-1.2 at 25℃
CAS DataBase Reference
87-39-8(CAS DataBase Reference)
EPA Substance Registry System
2,4,5,6(1H,3H)-Pyrimidinetetrone, 5-oxime (87-39-8)
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Safety

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
RTECS 
BA4225000
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

Precautionary statements

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P321Specific treatment (see … on this label).

P332+P313IF SKIN irritation occurs: Get medical advice/attention.

P362Take off contaminated clothing and wash before reuse.

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N-Bromosuccinimide Price

TRC
Product number
V634600
Product name
VioluricAcid
Packaging
2.5g
Price
$115
Updated
2021/12/16
TRC
Product number
V634600
Product name
VioluricAcid
Packaging
25g
Price
$525
Updated
2021/12/16
Medical Isotopes, Inc.
Product number
67480
Product name
VioluricAcid
Packaging
25g
Price
$1050
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
CHM0013570
Product name
ALLOXAN-5-OXIME
Purity
95.00%
Packaging
25G
Price
$1199.42
Updated
2021/12/16
Crysdot
Product number
CD11038820
Product name
5-(Hydroxyimino)pyrimidine-2,4,6(1H,3H,5H)-trione
Purity
97%
Packaging
10g
Price
$40
Updated
2021/12/16
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VIOLURIC ACID Chemical Properties,Usage,Production

Chemical Properties

LIGHT YELLOW CRYSTALLINE POWDER

Uses

Violuric Acid, can be used for the synthesis of some novel pyrimidines fused aza-heterocycles, having broad spectrum of pharmacological activities, such as 2-Methyloxazolo[5,4-d]pyrimidine-5,7(4H,6H)-dione (M324600).

Uses

Analytical reagent for chromatographic separation of cations. Forms chelates: Leermakers, Hoffman, J. Am. Chem. Soc. 80, 5663 (1958).

Reactions

Violuric acid readily deprotonated to give salts of the anion [ON=C(CONH)2CO]?, which are often deeply colored.

Flammability and Explosibility

Not classified

Synthesis

67-52-7

87-39-8

The general procedure for the synthesis of 5-(oxime-based)pyrimidine-2,4,6(1H,3H,5H)-trione from barbituric acid was as follows: firstly, 352 g of sodium nitrite was weighed and dissolved in 800 ml of deionized water to prepare an aqueous sodium nitrite solution for spare. In a 10L three-necked flask, 360g of sodium hydroxide and 4L of deionized water were added, and mechanical stirring was turned on until complete dissolution. When the temperature of the solution was reduced to about 30°C, 491 g of barbituric acid was added slowly to ensure that it was completely dissolved in the sodium hydroxide solution. Subsequently, the pre-prepared aqueous sodium nitrite solution was added to the reaction system, at which time the temperature of the mixed solution should be maintained between 10-15°C. Under continuous stirring, a mixed solution consisting of 1.2 L of concentrated hydrochloric acid and 2 L of deionized water was slowly added dropwise, and the rate of dropwise acceleration was controlled to maintain the reaction temperature in the range of 10-20 °C. During the dropwise addition, the formation of yellow-red solid and the release of orange gas were observed. After the dropwise addition, the temperature of the reaction system was adjusted to room temperature (25 °C) and the reaction was continued with stirring for about 16 hours. At the end of the reaction, the orange gas produced in the reaction was first removed. Then, the reaction solution was vacuum filtered using a vacuum pump and the filter cake was collected. The filter cake was washed sequentially with deionized water and a small amount of methanol, and finally dried under vacuum to obtain 513 g of the light purple target product 5-(oxime-based)pyrimidine-2,4,6(1H,3H,5H)-trione in a molar yield of 85.2%.

References

[1] Patent: CN108440419, 2018, A. Location in patent: Paragraph 0055; 0061; 0068; 0075
[2] Justus Liebigs Annalen der Chemie, 1864, vol. 130, p. 158
[3] Chemische Berichte, 1875, vol. 8, p. 613
[4] European Journal of Organic Chemistry, 2009, # 26, p. 4525 - 4533

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View Lastest Price from VIOLURIC ACID manufacturers

Hubei Lidu New Material Technology Co., Ltd
Product
VIOLURIC ACID 87-39-8
Price
US $0.00/g
Min. Order
1g
Purity
98%
Supply Ability
20tons
Release date
2024-09-19
Zhuozhou Wenxi import and Export Co., Ltd
Product
VIOLURIC ACID 87-39-8
Price
US $15.00-10.00/KG
Min. Order
1KG
Purity
99%+ HPLC
Supply Ability
Monthly supply of 1 ton
Release date
2021-08-11
Career Henan Chemical Co
Product
VIOLURIC ACID 87-39-8
Price
US $8.80/KG
Min. Order
1KG
Purity
97%-99%
Supply Ability
100kg
Release date
2019-07-04

87-39-8, VIOLURIC ACIDRelated Search:


  • ALLOXAN-5-OXIME
  • 5-ISONITROSOBARBITURIC ACID
  • 5-HYDROXYIMINOBARBITURIC ACID
  • 2,4,5,6(1H,3H)-Pyrimidinetetrone, 5-oxime
  • 2,4,5,6(1H,3H)-Pyrimidinetetrone,5-oxime
  • VIOLURIC ACID
  • 5-(Hydroxyimino)pyrimidine-2,4,6(1H,3H,5H)-trione
  • Violuric acid hydrate,95%
  • Alloxan-5-oxime 5-Isonitrosobarbituric Acid
  • Violuric Acid&nbsp
  • VLA
  • NSC 56338
  • 87-39-8 C4H3N3O4 VIOLURIC ACID
  • 87-39-8
  • CONHCONHCOCNOH