185698
Barbituric acid
99%, powder, ReagentPlus®
Synonym(s):
2,4,6-Trihydroxypyrimidine, Malonylurea
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About This Item
Empirical Formula (Hill Notation):
C4H4N2O3
CAS Number:
Molecular Weight:
128.09
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.21
EC Number:
200-658-0
MDL number:
Beilstein/REAXYS Number:
120502
Assay:
99%
Form:
powder
Product Name
Barbituric acid, ReagentPlus®, 99%
Quality Level
product line
ReagentPlus®
assay
99%
form
powder
mp
248-252 °C ((lit.)), 248-252 °C (dec.) (lit.)
SMILES string
[O=C1CC(=O)NC(=O)N1], O=C1CC(=O)NC(=O)N1
InChI
[1S/C4H4N2O3/c7-2-1-3(8)6-4(9)5-2/h1H2,(H2,5,6,7,8,9)], 1S/C4H4N2O3/c7-2-1-3(8)6-4(9)5-2/h1H2,(H2,5,6,7,8,9)
InChI key
[HNYOPLTXPVRDBG-UHFFFAOYSA-N], HNYOPLTXPVRDBG-UHFFFAOYSA-N
General description
Barbituric acid is a useful acid for organic and drug syntheses. Its dihydrate form can be synthesized from barbituric acid via crystallization from aqueous solution. Crystal structure of barbituric acid (in tautomeric form) has been investigated by a three dimensional fourier transform method. Its enol crystal form has been reported to be thermodynamically stable.
Application
Barbituric acid (BA) may be used in the preparation of the corresponding hemiaminals, via chemoselective reduction in the presence of SmI2/H2O reagent. It may be used in the preparation of BA- modified conjugated carbon nitride nanosheets.
It may be used to synthesize:
- 5-ylidenebarbituric acid derivatives via Knoevenagel condensation with aromatic and α,β-conjugated aromatic aldehydes
- 5-diaminomethylenebarbiturates by reacting with substituted carbodiimides
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
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Storage Class
11 - Combustible Solids
wgk
WGK 1
flash_point_f
302.0 °F - closed cup
flash_point_c
150.00 °C - closed cup
ppe
Eyeshields, Gloves, type N95 (US)
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Selective reduction of barbituric acids using SmI2/H2O: synthesis, reactivity, and structural analysis of tetrahedral adducts.
Michal Szostak et al.
Angewandte Chemie (International ed. in English), 52(48), 12559-12563 (2013-10-15)
A simple method for knoevenagel condensation of a, ?-conjugated and aromatic aldehydes with barbituric acid.
Jursic BS.
Journal of Heterocyclic Chemistry, 38(3), 655-657 (2001)
Photocatalytic reduction of CO2 by graphitic carbon nitride polymers derived from urea and barbituric acid.
Qin J, et al.
Applied Catalysis. B, Environmental, 179, 1-8 (2015)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 185698-25G | 04061835252848 |
| 185698-100G | 04061835252831 |
| 185698-500G | 04061835252855 |