BIUREA

BIUREA Basic information
Product Name:BIUREA
Synonyms:Ureidourea;ureidoureacarboxamide;BIUREA;DIUREA;hydrazine-1,2-dicarboxamide;N,Nzzhlxy-Dicarbamoylhydrazine;Biurea, 99% 100GR;dicarbamide
CAS:110-21-4
MF:C2H6N4O2
MW:118.09
EINECS:203-747-2
Product Categories:Pharmaceutical Intermediates;Aromatic Hydrazides, Hydrazines, Hydrazones and Oximes
Mol File:110-21-4.mol
BIUREA Structure
BIUREA Chemical Properties
Melting point 247-250 °C
Boiling point 220.6°C (rough estimate)
density 1.6040
refractive index 1.4462 (estimate)
storage temp. Sealed in dry,Room Temperature
solubility Sulfuric Acid (Sparingly, Heated)
pka10.06±0.43(Predicted)
form Solid
color White to Off-White
CAS DataBase Reference110-21-4(CAS DataBase Reference)
EPA Substance Registry SystemBiurea (110-21-4)
Safety Information
Risk Statements 36/37/38
Safety Statements 24/25
TSCA Yes
HazardClass IRRITANT
HS Code 29280000
Hazardous Substances Data110-21-4(Hazardous Substances Data)
ToxicityLD50 oral in rat: > 2gm/kg
MSDS Information
ProviderLanguage
ACROS English
ALFA English
BIUREA Usage And Synthesis
Chemical PropertiesWHITE POWDER
UsesHydrazine-1,2-dicarboxamide is a useful compound in the process of producing protected anode active material particles for rechargeable lithium batteries.
General DescriptionWhite powder.
Air & Water ReactionsInsoluble in water.
Reactivity ProfileBIUREA is chemically classified as an amide. Amides/imides react with azo and diazo compounds to generate toxic gases. Flammable gases are formed by the reaction of organic amides/imides with strong reducing agents. Amides are very weak bases (weaker than water). Imides are less basic yet and in fact react with strong bases to form salts. That is, they can react as acids. Mixing amides with dehydrating agents such as P2O5 or SOCl2 generates the corresponding nitrile. The combustion of these compounds generates mixed oxides of nitrogen (NOx).
Fire HazardThe flash point of BIUREA is not available, however BIUREA is probably non-flammable.
Purification MethodsCrystallise the diamide from water, wash the crystals with EtOH then Et2O and dry in vacuum over P2O5. It does not decompose on drying at 110o /48hours. Its solubility in H2O is 1% at 0o. [Andrieth & Mohr Inorg Synth IV 26 1953, Beilstein 3 H 116, 3 I 56, 3 III 229.]
BIUREA Preparation Products And Raw materials
Raw materialsUrea-->Hydrazinecarboxamide,2-(diphenylmethylene)--->BENZOPHENONE AZINE
Preparation ProductsAzodicarbonamide-->URAZOLE-->4-ethyl-1,2,4-triazolidine-3,5-dione
ETHYL 2-{1,2-BIS[(PROPYLAMINO)CARBONYL]HYDRAZINO}-1,3-THIAZOLE-4-CARBOXYLATE ETHYL 2-{1-{[(4-CHLOROPHENYL)AMINO]CARBONYL}-2-[(PROPYLAMINO)CARBONYL]HYDRAZINO}-1,3-THIAZOLE-4-CARBOXYLATE N~1~-PHENYL-1-[4-(4-CHLOROPHENYL)-1,3-THIAZOL-2-YL]-N~2~-CYCLOHEXYL-1,2-HYDRAZINEDICARBOXAMIDE N~1~-PHENYL-1-[4-(4-FLUOROPHENYL)-1,3-THIAZOL-2-YL]-N~2~-CYCLOHEXYL-1,2-HYDRAZINEDICARBOXAMIDE N~1~-PHENYL-1-[4-(4-METHYLPHENYL)-1,3-THIAZOL-2-YL]-N~2~-PHENYL-1,2-HYDRAZINEDICARBOXAMIDE ETHYL 2-{1-(ANILINOCARBONYL)-2-[(CYCLOHEXYLAMINO)CARBONYL]HYDRAZINO}-1,3-THIAZOLE-4-CARBOXYLATE ETHYL 2-{2-[(CYCLOHEXYLAMINO)CARBONYL]-1-[(PROPYLAMINO)CARBONYL]HYDRAZINO}-1,3-THIAZOLE-4-CARBOXYLATE BIUREA ETHYL 2-{1-[(CYCLOHEXYLAMINO)CARBONYL]-2-[(PROPYLAMINO)CARBONYL]HYDRAZINO}-1,3-THIAZOLE-4-CARBOXYLATE SALOR-INT L167975-1EA 1,2-HYDRAZINEDICARBOXAMIDE-13C2,15N2 N~1~-(4-CHLOROPHENYL)-1-[4-(4-METHYLPHENYL)-1,3-THIAZOL-2-YL]-N~2~-PHENYL-1,2-HYDRAZINEDICARBOXAMIDE N~1~-(4-CHLOROPHENYL)-1-[4-(4-FLUOROPHENYL)-1,3-THIAZOL-2-YL]-N~2~-CYCLOHEXYL-1,2-HYDRAZINEDICARBOXAMIDE N~1~-(4-METHYLPHENYL)-1-[4-(4-FLUOROPHENYL)-1,3-THIAZOL-2-YL]-N~2~-CYCLOHEXYL-1,2-HYDRAZINEDICARBOXAMIDE ETHYL 2-[2-[(CYCLOHEXYLAMINO)CARBONYL]-1-(4-TOLUIDINOCARBONYL)HYDRAZINO]-1,3-THIAZOLE-4-CARBOXYLATE N1-(4-CHLOROPHENYL)-1-(4-(4-CHLOROPHENYL)THIAZOL-2-YL)-N2-CYCLOHEXYLHYDRAZINE-1,2-DICARBOXAMIDE ETHYL 2-[2-[(PROPYLAMINO)CARBONYL]-1-(4-TOLUIDINOCARBONYL)HYDRAZINO]-1,3-THIAZOLE-4-CARBOXYLATE N~1~-(4-METHYLPHENYL)-1-[4-(4-METHYLPHENYL)-1,3-THIAZOL-2-YL]-N~2~-PHENYL-1,2-HYDRAZINEDICARBOXAMIDE

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