Product Name

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  • Name

    Hydrazine hydrate

  • EINECS 206-114-9
  • CAS No. 7803-57-8
  • Article Data13
  • CAS DataBase
  • Density 1.032
  • Solubility miscible
  • Melting Point -52 °C
  • Formula H4N2.H2O
  • Boiling Point 120-121 °C
  • Molecular Weight 50.0604
  • Flash Point 75 °C (167 °F)
  • Transport Information UN 3293 6.1/PG 3
  • Appearance colorless fuming liquid with a faint ammonia-like odor
  • Safety 53-45-60-61
  • Risk Codes 45-20/21/22-34-43-51/53-50/53-23/24/25-10
  • Molecular Structure Molecular Structure of 7803-57-8 (Hydrazine hydrate)
  • Hazard Symbols ToxicT,DangerousN
  • Synonyms Hydrazyna [Polish];RCRA waste no. U133;Hydrazines;Hydrazine base;Hydrazine, aqueous solution with not >37% hydrazine, by mass [UN3293] [Poison];Hydrazine hydrate 80%;hydrazine--water (1/1);RCRA waste number U133;Hydrazine, anhydrous or hydrazine aqueous solutions with >64% hydrazine, by mass [UN2029] [Corrosive];Diamine;Nitrogen hydride;Hydrazine monohydrate;Hydrazine (anhydrous);Hydrazine, anhydrous;Hydrazinehydrate;80%Hydrazinehydrade;NaAc;Hydrazines hydrate;Hydrazine hydrate80%;
  • PSA 61.27000
  • LogP 0.15510

Synthetic route

(1-phenylethylidene)hydrazine
13466-30-3

(1-phenylethylidene)hydrazine

moist air

moist air

A

hydrazine hydrate
7803-57-8

hydrazine hydrate

B

acetophenonazine
729-43-1

acetophenonazine

hydrogenchloride
7647-01-0

hydrogenchloride

formaldehyd
50-00-0

formaldehyd

hydrazinecarbodithioic acid methyl ester
5397-03-5

hydrazinecarbodithioic acid methyl ester

A

5-methylsulfanyl-[1,3,4]thiadiazole-3-carbodithioic acid methyl ester

5-methylsulfanyl-[1,3,4]thiadiazole-3-carbodithioic acid methyl ester

B

hydrazine hydrate
7803-57-8

hydrazine hydrate

sulfuric acid
7664-93-9

sulfuric acid

bis-[1-(6-hydroxy-[2]naphthyl)-ethylidene]-hydrazine

bis-[1-(6-hydroxy-[2]naphthyl)-ethylidene]-hydrazine

acetic acid
64-19-7

acetic acid

A

hydrazine hydrate
7803-57-8

hydrazine hydrate

B

6-aceto-naphthol-(2)

6-aceto-naphthol-(2)

N-amino-N',N''-diphenyl-guanidine
56004-08-1

N-amino-N',N''-diphenyl-guanidine

A

hydrazine hydrate
7803-57-8

hydrazine hydrate

B

aniline
62-53-3

aniline

C

triphenylguanazole

triphenylguanazole

Conditions
ConditionsYield
at 180℃;
hydroxide

hydroxide

hypochlorite
14380-61-1

hypochlorite

urea
57-13-6

urea

A

chloride
16887-00-6

chloride

B

carbonate(2-)
3812-32-6

carbonate(2-)

C

hydrazine hydrate
7803-57-8

hydrazine hydrate

Conditions
ConditionsYield
In not given in alk. soln.;
sodium hydrazide
13598-47-5

sodium hydrazide

A

hydrazine hydrate
7803-57-8

hydrazine hydrate

B

sodium hydroxide
1310-73-2

sodium hydroxide

Conditions
ConditionsYield
With ethanol; water In benzene byproducts: sodium alcoholate; decompn. of NaNH*NH2 without explosion: pouring greater amounts of dry benzene over NaNH*NH2 under N2 atmosphere, then addn. of small amounts of alcoholic benzene by shaking until solid substance has reacted; addn. of water;;
water
7732-18-5

water

butan-2-one azine
5921-54-0

butan-2-one azine

hydrazine hydrate
7803-57-8

hydrazine hydrate

Conditions
ConditionsYield
at 160 - 190℃; under 7500.75 - 8250.83 Torr; pH=8.2 - 8.5; Inert atmosphere; Industrial scale;
nitrogen
7727-37-9

nitrogen

A

ammonia
7664-41-7

ammonia

B

hydrazine hydrate
7803-57-8

hydrazine hydrate

Conditions
ConditionsYield
With potassium hydroxide In water at 20℃; under 760.051 Torr; Reagent/catalyst; Electrochemical reaction;
nitrogen
7727-37-9

nitrogen

water
7732-18-5

water

A

ammonia
7664-41-7

ammonia

B

hydrazine hydrate
7803-57-8

hydrazine hydrate

Conditions
ConditionsYield
With lithium perchlorate at 20℃; for 10h; pH=6.5; Reagent/catalyst; Electrochemical reaction;
nitrogen
7727-37-9

nitrogen

water
7732-18-5

water

hydrogen
1333-74-0

hydrogen

A

ammonia
7664-41-7

ammonia

B

hydrazine hydrate
7803-57-8

hydrazine hydrate

Conditions
ConditionsYield
With hydrogenchloride pH=1; Reagent/catalyst; Electrochemical reaction;
4-dimethylamino-benzaldehyde
100-10-7

4-dimethylamino-benzaldehyde

hydrazine hydrate
7803-57-8

hydrazine hydrate

Conditions
ConditionsYield
With hydrogenchloride In ethanol; water for 0.166667h;
nickel(II) chloride hexahydrate

nickel(II) chloride hexahydrate

hydrazine hydrate
7803-57-8

hydrazine hydrate

sodium hydroxide
1310-73-2

sodium hydroxide

nickel
7440-02-0

nickel

Conditions
ConditionsYield
In water N2H4*H2O (80%) added to aq. soln. of NiCl2*6H2O (temp. increased to 65°C) under vigorous stirring, cooling to 50°C, aq. NaOH (50%)added (temp. increased to 54°C), 1 h; ppt. washed with water and dried at room temp. for 16 h;100%
In water; ethylene glycol byproducts: N2, H2O; other Radiation; soln. of Ni compd. in ethylene glycol treated with hydrazine hydrate andNaOH under external magnetic field (0.13-0.35 T) with vigorous stirring , react at 60°C; pptd., septd., washed (ethanol), dried (vac., 40°C, 24 h), SEM, XRD;
praseodymium(III)-bis(octaethylporphyrinate)

praseodymium(III)-bis(octaethylporphyrinate)

hydrazine hydrate
7803-57-8

hydrazine hydrate

PrH(OEP)2

PrH(OEP)2

Conditions
ConditionsYield
In dichloromethane byproducts: N2; stirring at room temp. for 3 h; solvent and the excess of hydrazine hydrate evapd. (vac.); residue dried (50°C, 1 d);100%
(+)-(1S,11R)-[1-(2'-Aethylallyloxy)-2,2,3,3,7,7,8,8,11,12,12,13,13,17,17,18,18-heptadecamethyl-10,20-diaza-decahydroporphinato(2-)]-nickel

(+)-(1S,11R)-[1-(2'-Aethylallyloxy)-2,2,3,3,7,7,8,8,11,12,12,13,13,17,17,18,18-heptadecamethyl-10,20-diaza-decahydroporphinato(2-)]-nickel

hydrazine hydrate
7803-57-8

hydrazine hydrate

(+)-(1S,11R,2'RS)-[1-(2'-Methyl-1'-butoxy)-2,2,3,3,7,7,8,8,11,12,12,13,13,17,17,18,18-heptadecamethyl-10,20-diaza-decahydroporphinato(2-)]-nickel

(+)-(1S,11R,2'RS)-[1-(2'-Methyl-1'-butoxy)-2,2,3,3,7,7,8,8,11,12,12,13,13,17,17,18,18-heptadecamethyl-10,20-diaza-decahydroporphinato(2-)]-nickel

Conditions
ConditionsYield
With dihydrogen peroxide; copper(II) sulfate In tetrahydrofuran 30 % H2O2-soln. added for 20 min to Ni-complex, hydrazine monohydrate, CuSO4*5H2O in THF at 40°C; addn. of hexane, washing, filtration, evapn., drying at room temp., 0.01 Torr for 24 h;100%
[Zn(C20H2N4(CH3)4(C6H4OCH2CH2SCOCH3)2((CH2)5CH3)4)]
850620-67-6

[Zn(C20H2N4(CH3)4(C6H4OCH2CH2SCOCH3)2((CH2)5CH3)4)]

hydrazine hydrate
7803-57-8

hydrazine hydrate

[Zn(C20H2N4(CH3)4(C6H4OCH2CH2SH)2((CH2)5CH3)4)]
850620-58-5

[Zn(C20H2N4(CH3)4(C6H4OCH2CH2SH)2((CH2)5CH3)4)]

Conditions
ConditionsYield
In dichloromethane at 25°C;100%
(pS)-1-phthalimido-2-methylferrocene
1350636-34-8

(pS)-1-phthalimido-2-methylferrocene

hydrazine hydrate
7803-57-8

hydrazine hydrate

(pS)-1-amino-2-methylferrocene
1350890-19-5, 31760-79-9

(pS)-1-amino-2-methylferrocene

Conditions
ConditionsYield
In ethanol under Ar; N2H4 added via syringe to stirring soln. of Fe compd., refluxed for 2 h; added H2O, mixt. transferred into separatory funnel contg. H2O and (C2H5)2O, org. layer sepd., aq. layer extd. with addnl. (C2H5)2O, combined org. fractions dried over anhyd. Na2SO4 for 2 h, filtered, solvent removed(vac.);100%
methyl 2-(2,4-dimethyl-6-(pyridin-4-yl)phenoxy)acetate
1572184-86-1

methyl 2-(2,4-dimethyl-6-(pyridin-4-yl)phenoxy)acetate

hydrazine hydrate
7803-57-8

hydrazine hydrate

2-(2,4-dimethyl-6-(pyridin-3-yl)phenoxy)acetohydrazide
1572184-81-6

2-(2,4-dimethyl-6-(pyridin-3-yl)phenoxy)acetohydrazide

Conditions
ConditionsYield
In ethanol at 100℃; for 12h;100%
salicylaldehyde
90-02-8

salicylaldehyde

hydrazine hydrate
7803-57-8

hydrazine hydrate

benzil
134-81-6

benzil

cobalt(II) bromide

cobalt(II) bromide

nickel dibromide

nickel dibromide

Co2Ni((C6H4OCHN2(C6H5)C)2)2Br2(H2O)4*H2O
171201-92-6

Co2Ni((C6H4OCHN2(C6H5)C)2)2Br2(H2O)4*H2O

Conditions
ConditionsYield
In ethanol refluxing (2+1+1 h); cooling (room temp.), NaOH addn., pptn., filtration, washing (ethanol), drying; elem. anal.;99%
salicylaldehyde
90-02-8

salicylaldehyde

hydrazine hydrate
7803-57-8

hydrazine hydrate

benzil
134-81-6

benzil

copper(ll) bromide
7789-45-9

copper(ll) bromide

nickel dibromide

nickel dibromide

Cu2Ni((C6H4OCHN2(C6H5)C)2)2Br2(H2O)4*1.5H2O

Cu2Ni((C6H4OCHN2(C6H5)C)2)2Br2(H2O)4*1.5H2O

Conditions
ConditionsYield
In ethanol refluxing (2+1+1 h); cooling (room temp.), NaOH addn., pptn., filtration, washing (ethanol), drying; elem. anal.;99%
salicylaldehyde
90-02-8

salicylaldehyde

hydrazine hydrate
7803-57-8

hydrazine hydrate

benzil
134-81-6

benzil

nickel dibromide

nickel dibromide

Ni3((C6H4OCHN2(C6H5)C)2)2Br2
171201-89-1

Ni3((C6H4OCHN2(C6H5)C)2)2Br2

Conditions
ConditionsYield
In ethanol refluxing (2+1+1 h); cooling (room temp.), NaOH addn., pptn., filtration, washing (ethanol), drying; elem. anal.;99%
salicylaldehyde
90-02-8

salicylaldehyde

hydrazine hydrate
7803-57-8

hydrazine hydrate

benzil
134-81-6

benzil

cobalt(II) chloride
7646-79-9

cobalt(II) chloride

nickel dichloride

nickel dichloride

Co2Ni((C6H4OCHN2(C6H5)C)2)2Cl2(H2O)4*H2O
171201-91-5

Co2Ni((C6H4OCHN2(C6H5)C)2)2Cl2(H2O)4*H2O

Conditions
ConditionsYield
In ethanol refluxing (2+1+1 h); cooling (room temp.), NaOH addn., pptn., filtration, washing (ethanol), drying; elem. anal.;99%
salicylaldehyde
90-02-8

salicylaldehyde

hydrazine hydrate
7803-57-8

hydrazine hydrate

benzil
134-81-6

benzil

copper dichloride

copper dichloride

nickel dichloride

nickel dichloride

Cu2Ni((C6H4OCHN2(C6H5)C)2)2Cl2(H2O)4*1.5H2O

Cu2Ni((C6H4OCHN2(C6H5)C)2)2Cl2(H2O)4*1.5H2O

Conditions
ConditionsYield
In ethanol refluxing (2+1+1 h); cooling (room temp.), NaOH addn., pptn., filtration, washing (ethanol), drying; elem. anal.;99%
salicylaldehyde
90-02-8

salicylaldehyde

hydrazine hydrate
7803-57-8

hydrazine hydrate

benzil
134-81-6

benzil

nickel dichloride

nickel dichloride

Ni3((C6H4OCHN2(C6H5)C)2)2Cl2
171201-88-0

Ni3((C6H4OCHN2(C6H5)C)2)2Cl2

Conditions
ConditionsYield
In ethanol refluxing (2+1+1 h); cooling (room temp.), NaOH addn., pptn., filtration, washing (ethanol), drying; elem. anal.;99%
[((C5H5)Fe(C5H4C6H4N))2C6H4]

[((C5H5)Fe(C5H4C6H4N))2C6H4]

hydrazine hydrate
7803-57-8

hydrazine hydrate

[((C5H5)Fe(C5H4C6H4NH))2C6H4]*H2O

[((C5H5)Fe(C5H4C6H4NH))2C6H4]*H2O

Conditions
ConditionsYield
In not given99%
N-methyl-4-(methylamino)-3-nitro-N-phenylbenzene sulfonamide
1095501-93-1

N-methyl-4-(methylamino)-3-nitro-N-phenylbenzene sulfonamide

hydrazine hydrate
7803-57-8

hydrazine hydrate

3-amino-N-methyl-4-(methylamino)-N-phenylbenzene sulfonamide
1095501-96-4

3-amino-N-methyl-4-(methylamino)-N-phenylbenzene sulfonamide

Conditions
ConditionsYield
With activated charcoal; iron(III) chloride hexahydrate In isopropyl alcohol for 8h; boiling;99%
ammonium sulfate

ammonium sulfate

hydrazine hydrate
7803-57-8

hydrazine hydrate

magnesium
7439-95-4

magnesium

hydrazinium magnesium sulfate

hydrazinium magnesium sulfate

Conditions
ConditionsYield
byproducts: NH3, H2O, H2; at room temp.; EtOH added; elem. anal.;98%
tetrapotassium octacyanomolybdate(IV) dihydrate

tetrapotassium octacyanomolybdate(IV) dihydrate

water
7732-18-5

water

tetraphenyl phosphonium chloride
2001-45-8

tetraphenyl phosphonium chloride

hydrazine hydrate
7803-57-8

hydrazine hydrate

tetraphenylphosphonium amminetetracyanooxomolybdate(IV) dihydrate

tetraphenylphosphonium amminetetracyanooxomolybdate(IV) dihydrate

Conditions
ConditionsYield
In water byproducts: N2; Irradiation (UV/VIS); K4Mo(CN)8*2H2O (1.0 mmol) and PPh4Cl (0.67 mmol) dissolved in mixt. of N2H4*H2O (98%, 10 ml) and H2O (1 ml); exposed to sunlight; ppt. filtered off; dried in air; elem. anal.;98%
ethyl acetoacetate
141-97-9

ethyl acetoacetate

4-nitrobenzaldehdye
555-16-8

4-nitrobenzaldehdye

hydrazine hydrate
7803-57-8

hydrazine hydrate

malononitrile
109-77-3

malononitrile

6-amino-2,4-dihydro-4-(4-nitrophenyl)-3-methylpyrano[2,3-c]pyrazole-5-carbonitrile
89607-34-1, 879451-69-1

6-amino-2,4-dihydro-4-(4-nitrophenyl)-3-methylpyrano[2,3-c]pyrazole-5-carbonitrile

Conditions
ConditionsYield
With silica-supported tetramethylguanidine In neat (no solvent) at 100℃; for 0.333333h;98%
at 20℃; for 0.166667h; Ionic liquid; Inert atmosphere;92%
With trityl chloride In neat (no solvent) at 60℃; for 0.833333h;84%
With sodium sulfate; 4-[(R)-((2S,4S,5R)-5-ethenyl-1-azabicyclo-[2.2.2]octan-2-yl)(hydroxy)methyl]quinolin-6-ol In dichloromethane at 20℃; for 17h; optical yield given as %ee;80%
dibenzoyl(ferrocenylmethyl)methane
83267-90-7

dibenzoyl(ferrocenylmethyl)methane

hydrazine hydrate
7803-57-8

hydrazine hydrate

[1-H-3,5-Ph2-(C3N2)-CH2-(η5-C5H5)Fe(η5-C5H4)]
1194509-63-1

[1-H-3,5-Ph2-(C3N2)-CH2-(η5-C5H5)Fe(η5-C5H4)]

Conditions
ConditionsYield
In ethanol EtOH soln. of Fe compd. treated with excess N2H4*H2O (1:10 molar ratio),mixt. refluxed for 3 h; cooled to room temp., evapd., dissolved (CH2Cl2), chromd. (SiO2, CH2Cl2), evapd., dried (vac., 2 d), elem. anal.;98%
guanidine hydrochloride
50-01-1

guanidine hydrochloride

hydrazine hydrate
7803-57-8

hydrazine hydrate

triaminoguanidine hydrochloride
5329-29-3

triaminoguanidine hydrochloride

Conditions
ConditionsYield
In 1,4-dioxane for 2h; Reflux;98%
perfluorobenzaldehyde
653-37-2

perfluorobenzaldehyde

ethyl acetoacetate
141-97-9

ethyl acetoacetate

hydrazine hydrate
7803-57-8

hydrazine hydrate

malononitrile
109-77-3

malononitrile

6-amino-3-methyl-4-(2,3,4,5,6-pentafluorophenyl)-2,4-dihydropyrano[2,3-c]pyrazole-5-carbonitrile
354538-52-6, 879454-49-6

6-amino-3-methyl-4-(2,3,4,5,6-pentafluorophenyl)-2,4-dihydropyrano[2,3-c]pyrazole-5-carbonitrile

Conditions
ConditionsYield
With silica-supported tetramethylguanidine In neat (no solvent) at 100℃; for 0.25h;98%
ethyl acetoacetate
141-97-9

ethyl acetoacetate

4-chlorobenzaldehyde
104-88-1

4-chlorobenzaldehyde

hydrazine hydrate
7803-57-8

hydrazine hydrate

malononitrile
109-77-3

malononitrile

6‐amino‐4‐(4‐chlorophenyl)‐3‐methyl‐2,4-dihydropyrano[2.3‐c]pyrazol‐5‐carbonitrile
89607-39-6, 298217-11-5

6‐amino‐4‐(4‐chlorophenyl)‐3‐methyl‐2,4-dihydropyrano[2.3‐c]pyrazol‐5‐carbonitrile

Conditions
ConditionsYield
With silica-supported tetramethylguanidine In neat (no solvent) at 100℃; for 0.333333h;98%
With trityl chloride In neat (no solvent) at 60℃; for 0.833333h;82%

Hydrazine hydrate Standards and Recommendations

NIOSH REL: (Hydrazines) CL 0.03 ppm/120M

Hydrazine hydrate Specification

Hydrazine hydrate with cas registry number of 7803-57-8 is a colorless fuming liquid with a faint ammonia-like odor. It also has other registry numbers including 65209-65-6, 65492-74-2, 79785-97-0. Its EINECS registry number is 206-114-9. This chemical is stable, but incompatible with a wide variety of materials, including oxidizing agents, heavy metal oxides, dehydrating agents, alkali metals, rust, silver salts. It belongs to the following categories: Biochemistry; Reagents for Oligosaccharide Synthesis; Synthetic Organic Chemistry; Water Ttreatment Chemicals. In addition, this chemical has a systematic name which is called hydrazine hydrate (1:1). And its IUPAC name is called hydrazine hydrate.

The physical properties about this chemical are: (1)ACD/LogP: -1.20; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): -3.73; (4)ACD/LogD (pH 7.4): -2.04; (5)ACD/BCF (pH 5.5): 1; (6)ACD/BCF (pH 7.4): 1 ; (7)#H bond acceptors: 2; (8)#H bond donors: 4; (9)#Freely Rotating Bonds: 1; (10)Enthalpy of Vaporization: 41.8 kJ/mol; (11)Boiling Point: 113.5 °C at 760 mmHg; (12)Vapour Pressure: 20.7 mmHg at 25°C.

Preparation of Hydrazine hydrate: There are several methods to prepare this chemical. For example, it can be made by urea. First, mix the sodium hypochlorite and sodium hydroxide by a certain percentage. And add the mixture of urea and a small amount of potassium permanganate while stirring. Second, pass the steam directly into reactor at the temperature of 103 ~ 104 ℃. The oxidation reaction begins. Third, obtaine 40% hydrazine hydrate by fractional distillation and vacuum concentration. At last, 80% hydrazine hydrate is prepared by dehydration with caustic soda, vacuum distillation. The reaction is as follows:
NH2ONH2 + NaC1O +2 NaOH → N2H4.H2O + NaC1 + Na2CO3

Uses: It is used as reductant for hydrazine hydrate, medicine, pesticides, dyes, foaming agents, imaging agent, antioxidant materials. It is also used in the manufacture of high-purity metal, synthetic fiber, the separation of rare. In addition, the material can be used to manufacture rockets and explosives.

When you are using this chemical, please be cautious about it as the following:
This chemical causes burns. It also may cause cancer and sensitization by skin contact. The most important thing is that it is very toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment. Therefore, avoid exposure  before use. And avoid release to the environment. This material and its container must be disposed of as hazardous waste. In case of accident or if you feel unwell, seek medical advice immediately.

You can still convert the following datas into molecular structure:
(1)SMILES: O.NN;
(2)InChI: InChI=1/H4N2.H2O/c1-2;/h1-2H2;1H2;
(3)InChIKey: IKDUDTNKRLTJSI-UHFFFAOYAN

The toxicity data is as follows:

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
guinea pig LD50 oral 40mg/kg (40mg/kg) BEHAVIORAL: EXCITEMENT

BEHAVIORAL: MUSCLE CONTRACTION OR SPASTICITY)
Hygiene and Sanitation Vol. 30(7-9), Pg. 191, 1965.
mouse LD50 intraperitoneal 156mg/kg (156mg/kg)   Cancer Research. Vol. 41, Pg. 1469, 1981.
mouse LD50 oral 83mg/kg (83mg/kg) BEHAVIORAL: EXCITEMENT

BEHAVIORAL: MUSCLE CONTRACTION OR SPASTICITY)
Hygiene and Sanitation Vol. 30(7-9), Pg. 191, 1965.
rabbit LD50 oral 55mg/kg (55mg/kg) BEHAVIORAL: EXCITEMENT

BEHAVIORAL: MUSCLE CONTRACTION OR SPASTICITY)
Hygiene and Sanitation Vol. 30(7-9), Pg. 191, 1965.
rat LD50 oral 129mg/kg (129mg/kg) BEHAVIORAL: EXCITEMENT

BEHAVIORAL: MUSCLE CONTRACTION OR SPASTICITY)
Hygiene and Sanitation Vol. 30(7-9), Pg. 191, 1965.

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