Conditions | Yield |
---|---|
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; |
hydrazodicarboxamide
Conditions | Yield |
---|---|
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% |
Conditions | Yield |
---|---|
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% |
hydrazodicarboxamide
Conditions | Yield |
---|---|
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
A
hydrazodicarboxamide
B
(1E, 2E)-1,2-bis(3,4,5-trimethoxybenzylidene)hydrazine
Conditions | Yield |
---|---|
In tetrahydrofuran at 120 - 150℃; Rearrangement; elimination; | A n/a B 87% |
A
hydrazodicarboxamide
B
benzaldehyde benzylidenehydrazone
Conditions | Yield |
---|---|
In tetrahydrofuran at 120 - 150℃; Rearrangement; elimination; | A n/a B 85% |
3,4-methylenedioxybenzaldehyde semicarbazone
A
hydrazodicarboxamide
Conditions | Yield |
---|---|
In tetrahydrofuran at 120 - 150℃; Rearrangement; elimination; | A n/a B 84% |
(E)-2-(4-methoxybenzylidene)hydrazine carboxamide
A
hydrazodicarboxamide
B
N,N'-Bis-[1-(4-methoxy-phenyl)-meth-(E)-ylidene]-hydrazine
Conditions | Yield |
---|---|
In tetrahydrofuran at 120 - 150℃; Rearrangement; elimination; | A n/a B 83% |
A
hydrazodicarboxamide
B
(1E,2E)-1,2-bis(3,4-dimethoxybenzylidene)hydrazine
Conditions | Yield |
---|---|
In tetrahydrofuran at 120 - 150℃; Rearrangement; elimination; | A n/a B 68% |
N-acetoacetylphenylhydroxyloamine
A
hydrazodicarboxamide
B
N-Phenylhydroxylamine
C
1-carbamido-3-methyl-2-pyrazolin-5-one
D
azoxybenzene
Conditions | Yield |
---|---|
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
hydrazine carboxamide
A
hydrazodicarboxamide
B
Ethyloxamatcarbamylhydrazon
C
3-oxo-5-imino-6-ethoxycarbonyl-2,3,4,5-tetrahydro-1,2,4-triazine
D
3,5-diethoxycarbonyl-1,2,4-triazole
Conditions | Yield |
---|---|
In ethanol for 1h; Heating; | A 34% B 63% C 51% D 23% |
triethyl 1,3,5-triazine-2,4,6-tricarboxylate
A
hydrazodicarboxamide
B
Ethyloxamatcarbamylhydrazon
C
3-oxo-5-imino-6-ethoxycarbonyl-2,3,4,5-tetrahydro-1,2,4-triazine
D
3,5-diethoxycarbonyl-1,2,4-triazole
Conditions | Yield |
---|---|
With hydrazine carboxamide In ethanol for 1h; Heating; | A 34% B 63% C 51% D 23% |
Conditions | Yield |
---|---|
With hydrazine In hexane at 60℃; for 6h; | 62% |
semicarbazide hydrochloride
4-chloro-3-(1-chlorovinyl)-6-methyl-2-pyrone
A
hydrazodicarboxamide
B
3,6-dimethylpyrano<4,3-c>pyrazol-4(1H)-one
Conditions | Yield |
---|---|
With sodium acetate In ethanol for 21h; Heating; | A n/a B 49% |
Conditions | Yield |
---|---|
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℃; |
Conditions | Yield |
---|---|
In water for 0.75h; Heating; | 26% |
Conditions | Yield |
---|---|
beim Erhitzen; |
Conditions | Yield |
---|---|
at 240℃; | |
at 240℃; |
Conditions | Yield |
---|---|
With water; hydrazinium sulfate |
Conditions | Yield |
---|---|
With ethanol; water; potassium acetate |
carbamoyl azide
hydrazodicarboxamide
Conditions | Yield |
---|---|
at 110 - 120℃; und Kochen der Reaktionsprodukte mit Wasser; | |
With benzene at 100 - 115℃; und Kochen der Reaktionsprodukte mit Wasser; |
butan-2-one semicarbazone
A
urazole
B
hydrazodicarboxamide
C
butan-2-one azine
Conditions | Yield |
---|---|
beim Destillieren; |
Conditions | Yield |
---|---|
beim Erhitzen; |
ethanol
1-chloro-propan-2-one semicarbazone
A
hydroxy-acetone semicarbazone
B
hydrazodicarboxamide
Conditions | Yield |
---|---|
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% |
Conditions | Yield |
---|---|
With pyridine; p-toluenesulfonyl chloride In ethanol at 79 - 80℃; for 20h; Reagent/catalyst; Solvent; Temperature; Inert atmosphere; | 98% |
hydrazodicarboxamide
1-aminooctadecane
4-octadecyl-[1,2,4]triazolidine-3,5-dione
Conditions | Yield |
---|---|
In 1-methyl-pyrrolidin-2-one | 90% |
Conditions | Yield |
---|---|
With hydrogenchloride; sodium chloride In water at 320℃; for 0.216667h; | 89.9% |
Conditions | Yield |
---|---|
In water; acetone | 89% |
hexan-1-amine
hydrazodicarboxamide
4-hexyl-[1,2,4]triazolidine-3,5-dione
Conditions | Yield |
---|---|
With sodium hydroxide In N-methy pyrrolidone | 81% |
In 1-methyl-pyrrolidin-2-one | 81% |
hydrazodicarboxamide
4,4'-diaminodicyclohexylmethane
4,4'-bis-(1,2,4-triazolidine-3,5-dion-4-yl)-dicyclohexylmethane
Conditions | Yield |
---|---|
In 1-methyl-pyrrolidin-2-one; water | 75% |
hydrazodicarboxamide
Conditions | Yield |
---|---|
With pyridine; p-toluenesulfonyl chloride In N,N-dimethyl-formamide at 140℃; for 5h; Inert atmosphere; | 75% |
Conditions | Yield |
---|---|
With sodium hydroxide In 1-methyl-pyrrolidin-2-one | 70% |
In 1-methyl-pyrrolidin-2-one | 70% |
Conditions | Yield |
---|---|
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% |
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 (110-21-4) is used as the production of ADC foaming agent.
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. | orl-rat LD50:>2 g/kg | ATDAEI Acute Toxicity Data. Journal of the American College of Toxicology, Part B. 15 (Suppl 1),(1996),S92. |
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
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