Product Name

  • Name

    BIUREA

  • EINECS 203-747-2
  • CAS No. 110-21-4
  • Article Data120
  • CAS DataBase
  • Density 1.461g/cm3
  • Solubility
  • Melting Point 247-250 °C
  • Formula C2H6 N4 O2
  • Boiling Point °Cat760mmHg
  • Molecular Weight 118.095
  • Flash Point °C
  • Transport Information
  • Appearance WHITE POWDER
  • Safety Moderately toxic by ingestion. When heated to decomposition it emits toxic vapors of NOx.
  • Risk Codes 36/37/38
  • Molecular Structure Molecular Structure of 110-21-4 (BIUREA)
  • Hazard Symbols
  • Synonyms Biurea(6CI,7CI,8CI);1,1'-Hydrazobis(formamide);Bicarbamamide;Bicarbamimidic acid;Cellmic 142;Diurea;FE 823;HDCA;Hydradicarbonamide;Hydrazine,1,2-bis(aminocarbonyl)-;Hydrazine-N,N'-bis(carboxamide);Hydrazinedicarboxylicacid diamide;Hydrazocarbonamide;Hydrazodicarbamide;Hydrazodicarbonamide;Hydrazodicarboxamide;KBH 30;LDA;LDA (fire retardant);N,N'-Biscarbamoylhydrazine;NSC 1897;S 3176;Ureidourea;
  • PSA 110.24000
  • LogP 0.42040

Synthetic route

Azodicarboxamid
123-77-3

Azodicarboxamid

hydrazodicarboxamide
110-21-4

hydrazodicarboxamide

Conditions
ConditionsYield
With hydrazine hydrate In acetonitrile at 20℃; for 1.5h;98%
With hydrogen sulfide; water beim Kochen;
With hydrogenchloride beim Kochen;
With water; sodium carbonate beim Kochen;
sodium chlorobiuret salt

sodium chlorobiuret salt

hydrazodicarboxamide
110-21-4

hydrazodicarboxamide

Conditions
ConditionsYield
With ammonia; aluminum (III) chloride; zinc(II) chloride In water at 10 - 60℃; for 1h;97%
With ammonia; aluminum (III) chloride; zinc(II) chloride In water at 10 - 60℃; for 1h;96%
With ammonia; cadmium(II) chloride; zinc(II) chloride In water at 10 - 60℃; for 1h;96%
BIURET
108-19-0

BIURET

hydrazodicarboxamide
110-21-4

hydrazodicarboxamide

Conditions
ConditionsYield
Stage #1: BIURET With sodium hypochlorite In water at 5 - 10℃;
Stage #2: With ammonia; zinc(II) chloride In water at 100℃; for 0.5h; Product distribution / selectivity;
96%
Stage #1: BIURET With sodium hypochlorite In water at 5 - 10℃;
Stage #2: With ammonia In water at 100℃; for 0.5h; Product distribution / selectivity;
95%
Stage #1: BIURET With sodium hypochlorite In ethanol; water at 5 - 10℃;
Stage #2: With ammonia In ethanol; water at 100℃; for 0.5h; Product distribution / selectivity;
85%
chlorobiuret sodium salt

chlorobiuret sodium salt

hydrazodicarboxamide
110-21-4

hydrazodicarboxamide

Conditions
ConditionsYield
With ammonia; zinc(II) chloride In water at 10 - 100℃; for 0.5h; Product distribution / selectivity;93%
With ammonia; hydrogenchloride In water at 10 - 100℃; for 0.5h; Product distribution / selectivity;92%
With ammonia; nickel diacetate In water at 10 - 100℃; for 0.5h; Product distribution / selectivity;92%
With ammonia In water at 10 - 100℃; for 0.5h; Product distribution / selectivity;87%
(E)-2-(3,4,5-trimethoxybenzylidene)hydrazine carboxamide
81824-93-3

(E)-2-(3,4,5-trimethoxybenzylidene)hydrazine carboxamide

A

hydrazodicarboxamide
110-21-4

hydrazodicarboxamide

B

(1E, 2E)-1,2-bis(3,4,5-trimethoxybenzylidene)hydrazine
7251-01-6

(1E, 2E)-1,2-bis(3,4,5-trimethoxybenzylidene)hydrazine

Conditions
ConditionsYield
In tetrahydrofuran at 120 - 150℃; Rearrangement; elimination;A n/a
B 87%
(E)-2-benzylidenehydrazine-1-carboxamide

(E)-2-benzylidenehydrazine-1-carboxamide

A

hydrazodicarboxamide
110-21-4

hydrazodicarboxamide

B

benzaldehyde benzylidenehydrazone
28867-76-7

benzaldehyde benzylidenehydrazone

Conditions
ConditionsYield
In tetrahydrofuran at 120 - 150℃; Rearrangement; elimination;A n/a
B 85%
3,4-methylenedioxybenzaldehyde semicarbazone
16742-62-4

3,4-methylenedioxybenzaldehyde semicarbazone

A

hydrazodicarboxamide
110-21-4

hydrazodicarboxamide

B

(2E,N'E)-3-(benzo[d][1,3]dioxol-5-yl)-N'-(benzo[d][1,3]dioxol-5-ylmethylene)-2-cyanoacrylohydrazide

(2E,N'E)-3-(benzo[d][1,3]dioxol-5-yl)-N'-(benzo[d][1,3]dioxol-5-ylmethylene)-2-cyanoacrylohydrazide

Conditions
ConditionsYield
In tetrahydrofuran at 120 - 150℃; Rearrangement; elimination;A n/a
B 84%
(E)-2-(4-methoxybenzylidene)hydrazine carboxamide
120445-53-6

(E)-2-(4-methoxybenzylidene)hydrazine carboxamide

A

hydrazodicarboxamide
110-21-4

hydrazodicarboxamide

B

N,N'-Bis-[1-(4-methoxy-phenyl)-meth-(E)-ylidene]-hydrazine
41097-47-6

N,N'-Bis-[1-(4-methoxy-phenyl)-meth-(E)-ylidene]-hydrazine

Conditions
ConditionsYield
In tetrahydrofuran at 120 - 150℃; Rearrangement; elimination;A n/a
B 83%
2,4-dimethoxybenzaldehyde semicarbazone

2,4-dimethoxybenzaldehyde semicarbazone

A

hydrazodicarboxamide
110-21-4

hydrazodicarboxamide

B

(1E,2E)-1,2-bis(3,4-dimethoxybenzylidene)hydrazine
134691-71-7

(1E,2E)-1,2-bis(3,4-dimethoxybenzylidene)hydrazine

Conditions
ConditionsYield
In tetrahydrofuran at 120 - 150℃; Rearrangement; elimination;A n/a
B 68%
N-acetoacetylphenylhydroxyloamine
27991-08-8

N-acetoacetylphenylhydroxyloamine

A

hydrazodicarboxamide
110-21-4

hydrazodicarboxamide

B

N-Phenylhydroxylamine
100-65-2

N-Phenylhydroxylamine

C

1-carbamido-3-methyl-2-pyrazolin-5-one
57303-41-0

1-carbamido-3-methyl-2-pyrazolin-5-one

D

azoxybenzene
495-48-7

azoxybenzene

Conditions
ConditionsYield
With semicarbazide hydrochloride; sodium carbonate In ethanol for 24h; Ambient temperature; Further byproducts given;A 63%
B 35%
C 15.5%
D 30%
triethyl 1,3,5-triazine-2,4,6-tricarboxylate
898-22-6

triethyl 1,3,5-triazine-2,4,6-tricarboxylate

hydrazine carboxamide
4426-72-6, 51433-48-8

hydrazine carboxamide

A

hydrazodicarboxamide
110-21-4

hydrazodicarboxamide

B

Ethyloxamatcarbamylhydrazon
57041-78-8

Ethyloxamatcarbamylhydrazon

C

3-oxo-5-imino-6-ethoxycarbonyl-2,3,4,5-tetrahydro-1,2,4-triazine
95234-60-9

3-oxo-5-imino-6-ethoxycarbonyl-2,3,4,5-tetrahydro-1,2,4-triazine

D

3,5-diethoxycarbonyl-1,2,4-triazole
91173-78-3

3,5-diethoxycarbonyl-1,2,4-triazole

Conditions
ConditionsYield
In ethanol for 1h; Heating;A 34%
B 63%
C 51%
D 23%
triethyl 1,3,5-triazine-2,4,6-tricarboxylate
898-22-6

triethyl 1,3,5-triazine-2,4,6-tricarboxylate

A

hydrazodicarboxamide
110-21-4

hydrazodicarboxamide

B

Ethyloxamatcarbamylhydrazon
57041-78-8

Ethyloxamatcarbamylhydrazon

C

3-oxo-5-imino-6-ethoxycarbonyl-2,3,4,5-tetrahydro-1,2,4-triazine
95234-60-9

3-oxo-5-imino-6-ethoxycarbonyl-2,3,4,5-tetrahydro-1,2,4-triazine

D

3,5-diethoxycarbonyl-1,2,4-triazole
91173-78-3

3,5-diethoxycarbonyl-1,2,4-triazole

Conditions
ConditionsYield
With hydrazine carboxamide In ethanol for 1h; Heating;A 34%
B 63%
C 51%
D 23%
trimethylsilyl isocyanate
1118-02-1

trimethylsilyl isocyanate

hydrazodicarboxamide
110-21-4

hydrazodicarboxamide

Conditions
ConditionsYield
With hydrazine In hexane at 60℃; for 6h;62%
semicarbazide hydrochloride
563-41-7

semicarbazide hydrochloride

4-chloro-3-(1-chlorovinyl)-6-methyl-2-pyrone
106089-51-4

4-chloro-3-(1-chlorovinyl)-6-methyl-2-pyrone

A

hydrazodicarboxamide
110-21-4

hydrazodicarboxamide

B

3,6-dimethylpyrano<4,3-c>pyrazol-4(1H)-one
106089-56-9

3,6-dimethylpyrano<4,3-c>pyrazol-4(1H)-one

Conditions
ConditionsYield
With sodium acetate In ethanol for 21h; Heating;A n/a
B 49%
semicarbazide hydrochloride
563-41-7

semicarbazide hydrochloride

hydrazodicarboxamide
110-21-4

hydrazodicarboxamide

Conditions
ConditionsYield
With ethyl acetoacetate In water a) from 5 deg C to 10 deg C, 15 min, b) reflux, 3 h;37%
With water; sodium carbonate
With selenium(IV) oxide; water at 60℃;
3,5-dimethylpyrazole-1-carboxamide
934-48-5

3,5-dimethylpyrazole-1-carboxamide

hydrazodicarboxamide
110-21-4

hydrazodicarboxamide

Conditions
ConditionsYield
In water for 0.75h; Heating;26%
acetophenone semicarbazone
2492-30-0

acetophenone semicarbazone

hydrazodicarboxamide
110-21-4

hydrazodicarboxamide

Conditions
ConditionsYield
beim Erhitzen;
acetophenone semicarbazone
2492-30-0

acetophenone semicarbazone

A

hydrazodicarboxamide
110-21-4

hydrazodicarboxamide

B

acetophenonazine
729-43-1

acetophenonazine

Conditions
ConditionsYield
at 240℃;
at 240℃;
bromocyane
506-68-3

bromocyane

hydrazodicarboxamide
110-21-4

hydrazodicarboxamide

Conditions
ConditionsYield
With water; hydrazinium sulfate
phorone
504-20-1

phorone

semicarbazide hydrochloride
563-41-7

semicarbazide hydrochloride

A

hydrazodicarboxamide
110-21-4

hydrazodicarboxamide

B

2,6-dimethyl-6-semicarbazido-hept-2-en-4-one semicarbazone

2,6-dimethyl-6-semicarbazido-hept-2-en-4-one semicarbazone

Conditions
ConditionsYield
With ethanol; water; potassium acetate
carbamoyl azide
13125-56-9

carbamoyl azide

hydrazodicarboxamide
110-21-4

hydrazodicarboxamide

Conditions
ConditionsYield
at 110 - 120℃; und Kochen der Reaktionsprodukte mit Wasser;
With benzene at 100 - 115℃; und Kochen der Reaktionsprodukte mit Wasser;
butan-2-one semicarbazone
624-46-4

butan-2-one semicarbazone

A

urazole
3232-84-6

urazole

B

hydrazodicarboxamide
110-21-4

hydrazodicarboxamide

C

butan-2-one azine
5921-54-0

butan-2-one azine

Conditions
ConditionsYield
beim Destillieren;
butan-2-one semicarbazone
624-46-4

butan-2-one semicarbazone

hydrazodicarboxamide
110-21-4

hydrazodicarboxamide

Conditions
ConditionsYield
beim Erhitzen;
bromo-acetone semicarbazone

bromo-acetone semicarbazone

ethanol
64-17-5

ethanol

A

hydroxy-acetone semicarbazone
21178-87-0

hydroxy-acetone semicarbazone

B

hydrazodicarboxamide
110-21-4

hydrazodicarboxamide

4-semicarbazido-pentan-2-one semicarbazone

4-semicarbazido-pentan-2-one semicarbazone

ethanol
64-17-5

ethanol

hydrazodicarboxamide
110-21-4

hydrazodicarboxamide

ethanol
64-17-5

ethanol

1-chloro-propan-2-one semicarbazone
53646-01-8

1-chloro-propan-2-one semicarbazone

A

hydroxy-acetone semicarbazone
21178-87-0

hydroxy-acetone semicarbazone

B

hydrazodicarboxamide
110-21-4

hydrazodicarboxamide

ethanol
64-17-5

ethanol

6-methyl-4-semicarbazido-heptan-2-one semicarbazone

6-methyl-4-semicarbazido-heptan-2-one semicarbazone

hydrazodicarboxamide
110-21-4

hydrazodicarboxamide

ethanol
64-17-5

ethanol

2-(1-semicarbazido-ethyl)-3-semicarbazono-butyric acid ethyl ester

2-(1-semicarbazido-ethyl)-3-semicarbazono-butyric acid ethyl ester

hydrazodicarboxamide
110-21-4

hydrazodicarboxamide

cyanic acid
420-05-3

cyanic acid

hydrazodicarboxamide
110-21-4

hydrazodicarboxamide

hydrazodicarboxamide
110-21-4

hydrazodicarboxamide

Azodicarboxamid
123-77-3

Azodicarboxamid

Conditions
ConditionsYield
With acetic acid; copper(I) bromide at 20℃; under 760.051 Torr; for 12h; Reagent/catalyst; Temperature; Sealed tube;99%
With tetra-N-butylammonium tribromide; sodium nitrite In 1,2-dimethoxyethane; water at 65℃; under 760.051 Torr; for 20h; Reagent/catalyst; Solvent; Pressure; Temperature; Sealed tube;98%
With hydrogenchloride; iron(III) chloride; dihydrogen peroxide; ozone In water at 40℃; pH=2 - 5; Temperature;97.4%
hydrazodicarboxamide
110-21-4

hydrazodicarboxamide

1,3,4-oxadiazole-2,5-diamine
2937-79-3

1,3,4-oxadiazole-2,5-diamine

Conditions
ConditionsYield
With pyridine; p-toluenesulfonyl chloride In ethanol at 79 - 80℃; for 20h; Reagent/catalyst; Solvent; Temperature; Inert atmosphere;98%
stannous octoate

stannous octoate

hydrazodicarboxamide
110-21-4

hydrazodicarboxamide

1-aminooctadecane
124-30-1

1-aminooctadecane

4-octadecyl-[1,2,4]triazolidine-3,5-dione
81329-56-8

4-octadecyl-[1,2,4]triazolidine-3,5-dione

Conditions
ConditionsYield
In 1-methyl-pyrrolidin-2-one90%
2,3-diaminephenazine
655-86-7

2,3-diaminephenazine

hydrazodicarboxamide
110-21-4

hydrazodicarboxamide

phenazine benzimidazolone
106050-79-7

phenazine benzimidazolone

Conditions
ConditionsYield
With hydrogenchloride; sodium chloride In water at 320℃; for 0.216667h;89.9%
1-methyl-pyrrolidin-2-one
872-50-4

1-methyl-pyrrolidin-2-one

hydrazodicarboxamide
110-21-4

hydrazodicarboxamide

urazole
3232-84-6

urazole

Conditions
ConditionsYield
In water; acetone89%
hexan-1-amine
111-26-2

hexan-1-amine

hydrazodicarboxamide
110-21-4

hydrazodicarboxamide

4-hexyl-[1,2,4]triazolidine-3,5-dione
81329-55-7

4-hexyl-[1,2,4]triazolidine-3,5-dione

Conditions
ConditionsYield
With sodium hydroxide In N-methy pyrrolidone81%
In 1-methyl-pyrrolidin-2-one81%
hydrazodicarboxamide
110-21-4

hydrazodicarboxamide

4,4'-diaminodicyclohexylmethane
1761-71-3

4,4'-diaminodicyclohexylmethane

4,4'-bis-(1,2,4-triazolidine-3,5-dion-4-yl)-dicyclohexylmethane
81529-52-4

4,4'-bis-(1,2,4-triazolidine-3,5-dion-4-yl)-dicyclohexylmethane

Conditions
ConditionsYield
In 1-methyl-pyrrolidin-2-one; water75%
hydrazodicarboxamide
110-21-4

hydrazodicarboxamide

2,3-dihydro-[1,3,4]-oxadiazole-2,5-diamine

2,3-dihydro-[1,3,4]-oxadiazole-2,5-diamine

Conditions
ConditionsYield
With pyridine; p-toluenesulfonyl chloride In N,N-dimethyl-formamide at 140℃; for 5h; Inert atmosphere;75%
hydrazodicarboxamide
110-21-4

hydrazodicarboxamide

benzylamine
100-46-9

benzylamine

4-benzyl-1,2,4-triazolidine-3,5-dione
16312-86-0

4-benzyl-1,2,4-triazolidine-3,5-dione

Conditions
ConditionsYield
With sodium hydroxide In 1-methyl-pyrrolidin-2-one70%
In 1-methyl-pyrrolidin-2-one70%
hydrazodicarboxamide
110-21-4

hydrazodicarboxamide

A

sodium hypochlorite
7681-52-9

sodium hypochlorite

B

sodium azide

sodium azide

C

hydrogen azide
916329-38-9

hydrogen azide

Conditions
ConditionsYield
With sodium hydroxide; sulfuric acid In water ice cooling; distn. with H2SO4;A n/a
B n/a
C 9%
With NaOH; H2SO4 In water ice cooling; distn. with H2SO4;A n/a
B n/a
C 9%

1,2-HYDRAZINEDICARBOXAMIDE Chemical Properties

IUPAC Name: 1,2-Hydrazinedicarboxamide
The MF of 1,2-Hydrazinedicarboxamide (110-21-4) is C2H6N4O2.

                             
The MW of 1,2-Hydrazinedicarboxamide (110-21-4) is 118.09.
Synonyms of 1,2-Hydrazinedicarboxamide (110-21-4): Hydrazine-1,2-dicarboxamide ; 1, 2-Hydrazinedicarboxamide ; 1,1'-Hydrazinebisformamide ; 1,1-Hydrazoformamide 
Product Categories: Pharmaceutical Intermediates;Hydrazines,Hydrazones and Oximes
Apperance: White powder
Index of Refraction: 1.547 
Density: 1.461 g/ml
EINECS: 203-747-2
Melting Point: 239-241 °C

1,2-HYDRAZINEDICARBOXAMIDE Uses

   1,2-Hydrazinedicarboxamide (110-21-4) is used as the production of ADC foaming agent.

1,2-HYDRAZINEDICARBOXAMIDE Production

It 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).

1,2-HYDRAZINEDICARBOXAMIDE Toxicity Data With Reference

1.    

orl-rat LD50:>2 g/kg

    ATDAEI    Acute Toxicity Data. Journal of the American College of Toxicology, Part B. 15 (Suppl 1),(1996),S92.

1,2-HYDRAZINEDICARBOXAMIDE Safety Profile

Moderately toxic by ingestion. When heated to decomposition it emits toxic vapors of NOx.Safety information of 1,2-Hydrazinedicarboxamide (110-21-4):
Risk Statements 
36/37/38  Irritating to eyes, respiratory system and skin
Safety Statements
24/25  Avoid contact with skin and eyes

Post buying leads

About|Contact|Cas|Product Name|Molecular|Country|Encyclopedia

Message|New Cas|MSDS|Service|Advertisement|CAS DataBase|Article Data|Manufacturers | Chemical Catalog

©2008 LookChem.com,License: ICP

NO.:Zhejiang16009103

complaints:service@lookchem.com Desktop View