Product Name

  • Name

    Ammonium formate

  • EINECS 208-753-9
  • CAS No. 540-69-2
  • Article Data71
  • CAS DataBase
  • Density 1.26 g/cm3
  • Solubility H2O: 10 M at 20 °C, clear, colorless
  • Melting Point 119-121 °C(lit.)
  • Formula NH4HCO2
  • Boiling Point 100.6oC at 760 mmHg
  • Molecular Weight 63.0562
  • Flash Point 29.9oC
  • Transport Information
  • Appearance colorless, hygroscopic, crystalline solid
  • Safety 26-36-37/39
  • Risk Codes 36/37/38
  • Molecular Structure Molecular Structure of 540-69-2 (Ammonium formate)
  • Hazard Symbols IrritantXi
  • Synonyms Ammoniumformate (6CI);Formic acid, ammonium salt (8CI,9CI);
  • PSA 40.54000
  • LogP 0.66060

Synthetic route

hydrogen cyanide
74-90-8

hydrogen cyanide

ammonium formate
540-69-2

ammonium formate

Conditions
ConditionsYield
With water In hydrogenchloride Kinetics; at 35 45 and 65°C;
With hydrogen bromide In hydrogen bromide Kinetics;
explosive decomposition;
acetylacetaldehyde dimethyl acetal
5436-21-5

acetylacetaldehyde dimethyl acetal

A

4-Methylpyrimidine
3438-46-8

4-Methylpyrimidine

B

methanol
67-56-1

methanol

C

ammonium formate
540-69-2

ammonium formate

Conditions
ConditionsYield
at 190℃; for 3.5h;A 79%
B n/a
C n/a
formic acid
64-18-6

formic acid

ammonia
7664-41-7

ammonia

ammonium formate
540-69-2

ammonium formate

Conditions
ConditionsYield
In diethyl ether introduction of dry NH3 into ethereal soln. of HCO2H; recrystallizing from ethanol;
In not given introduction of gaseous NH3 into 90 % HCO2H soln., finishing by higher temperature; recrystallizing from dry alcohol, drying over H2SO4 in vacuum desiccator;
In water neutralization of aq. HCO2H with NH3, evaporation, concentration in vacuo;
ammonium hydrogencarbonate

ammonium hydrogencarbonate

ammonium formate
540-69-2

ammonium formate

Conditions
ConditionsYield
With water; nickel at 125 - 200℃; under 73550.8 - 330978 Torr; Hydrogenation;
carbon monoxide
201230-82-2

carbon monoxide

ammonia
7664-41-7

ammonia

ammonium formate
540-69-2

ammonium formate

Conditions
ConditionsYield
With water In gas by higher temperature;
In water
With H2O In neat (no solvent, gas phase) by higher temperature;
In water
With water In gas by higher temperature;
carbon monoxide

carbon monoxide

ammonium formate
540-69-2

ammonium formate

Conditions
ConditionsYield
With ammonia; water at 160 - 220℃; under 117681 - 279493 Torr;
carbon dioxide
124-38-9

carbon dioxide

ammonia
7664-41-7

ammonia

ammonium formate
540-69-2

ammonium formate

Conditions
ConditionsYield
In gas
in present of catalysts;
With H2 In water
ethanedinitrile
460-19-5

ethanedinitrile

ammonium formate
540-69-2

ammonium formate

Conditions
ConditionsYield
With H2O In water further products; in alkaline soln.;
With H2O In water further products; in alkaline soln.;
carbon monoxide
201230-82-2

carbon monoxide

ammonium formate
540-69-2

ammonium formate

Conditions
ConditionsYield
With nitrogen; water; hydrogen In gas dark electric discharge in a gaseous mixture of N2, H2, H2O, CO and CO2;
With N2; H2; H2O In neat (no solvent, gas phase) dark electric discharge in a gaseous mixture of N2, H2, H2O, CO and CO2;
H3PO4*HCN

H3PO4*HCN

A

phosphoric acid
86119-84-8, 7664-38-2

phosphoric acid

B

ammonium formate
540-69-2

ammonium formate

Conditions
ConditionsYield
With water In water
With H2O In water
ammonium bicarbonate
1066-33-7

ammonium bicarbonate

ammonium formate
540-69-2

ammonium formate

Conditions
ConditionsYield
With H2; catalyst: (RuCl2(benzene))2/dppm In tetrahydrofuran; water 2 h at 70°C at 50 bar H2; detd. by NMR;
potassium hexacyanoferrate(III)

potassium hexacyanoferrate(III)

A

potassium carbonylpentacyanoferrate(II)

potassium carbonylpentacyanoferrate(II)

B

carbon dioxide
124-38-9

carbon dioxide

C

ammonium formate
540-69-2

ammonium formate

D

ammonium bicarbonate
1066-33-7

ammonium bicarbonate

Conditions
ConditionsYield
With carbon monoxide In water aq. soln. in sealed tube (130°C); excess of CO;;
potassium hexacyanoferrate(III)

potassium hexacyanoferrate(III)

A

potassium iron(III) hexacyanoferrate(II)

potassium iron(III) hexacyanoferrate(II)

B

carbon dioxide
124-38-9

carbon dioxide

C

ammonium formate
540-69-2

ammonium formate

D

potassium ferrocyanide

potassium ferrocyanide

Conditions
ConditionsYield
With carbon monoxide In water aq. soln. in sealed tube (130°C);;
CYANAMID
420-04-2

CYANAMID

ammonium formate
540-69-2

ammonium formate

Conditions
ConditionsYield
In water Electrolysis;
In water Electrolysis;
carbon dioxide
124-38-9

carbon dioxide

ammonium formate
540-69-2

ammonium formate

Conditions
ConditionsYield
With ammonium amalgame
With ammonium amalgame
formic acid
64-18-6

formic acid

aluminium nitride

aluminium nitride

ammonium formate
540-69-2

ammonium formate

Conditions
ConditionsYield
In water
In water
2Fe(2+)*5Fe(3+)*19CN(1-)=2Fe(CN)2*5Fe(CN)3

2Fe(2+)*5Fe(3+)*19CN(1-)=2Fe(CN)2*5Fe(CN)3

A

ammonium carbonate

ammonium carbonate

B

ammonium formate
540-69-2

ammonium formate

Conditions
ConditionsYield
In neat (no solvent) decomposition at 120°C; further byproducts;;
In neat (no solvent) decomposition at 120°C; further byproducts;;
H3PO4*HCN

H3PO4*HCN

ammonium formate
540-69-2

ammonium formate

Conditions
ConditionsYield
In water byproducts: H3PO4; hydrolysis;
HCN*H2SO4

HCN*H2SO4

ammonium formate
540-69-2

ammonium formate

Conditions
ConditionsYield
With air byproducts: H2SO4; hydrolysis;
ammonium oxalate
1113-38-8

ammonium oxalate

A

ethanedinitrile
460-19-5

ethanedinitrile

B

ammonium formate
540-69-2

ammonium formate

Conditions
ConditionsYield
With glycerol beim Erhitzen; Nebenprod.2:Ammonium-carbonat; Nebenprod.3:Ammonium-cyanid;
hydrogen cyanide
74-90-8

hydrogen cyanide

hydrogen bromide
10035-10-6, 12258-64-9

hydrogen bromide

ammonium formate
540-69-2

ammonium formate

Conditions
ConditionsYield
at 45℃; Kinetics; Hydrolysis;
carbon dioxide
124-38-9

carbon dioxide

sodium formate
141-53-7

sodium formate

ammonium formate
540-69-2

ammonium formate

Conditions
ConditionsYield
With ammonia; water
carbon dioxide
124-38-9

carbon dioxide

calcium diformate
544-17-2

calcium diformate

ammonium formate
540-69-2

ammonium formate

Conditions
ConditionsYield
With ammonia
carbon dioxide
124-38-9

carbon dioxide

ammonia
7664-41-7

ammonia

sodium formate
141-53-7

sodium formate

ammonium formate
540-69-2

ammonium formate

Conditions
ConditionsYield
In not given byproducts: NaHCO3; introduction of NH3 and CO2 into technical sodium formate soln.;
ammonium carbonate monohydrate

ammonium carbonate monohydrate

ammonium formate
540-69-2

ammonium formate

Conditions
ConditionsYield
Electrolysis; electrolysis of a soln. of 800 g (NH4)2CO3 in 3200 cm^3 H2O and 880 cm^3 aq.NH3 (D=0.910) with diaphragm; cathode:zinc; anode:platinum; no reduction with Pb,NI,Fe,Cu,Pt cathode;
Electrolysis; electrolysis of a soln. of 800 g (NH4)2CO3 in 3200 cm^3 H2O and 880 cm^3 aq.NH3 (D=0.910) with diaphragm; cathode:zinc; anode:platinum; no reduction with Pb,NI,Fe,Cu,Pt cathode;
barium cyanide

barium cyanide

water
7732-18-5

water

ammonium formate
540-69-2

ammonium formate

Conditions
ConditionsYield
saponification of Ba(CN)2 with water; precipitating of Ba with CO2;
saponification of Ba(CN)2 with water; precipitating of Ba with CO2;
nitromethane
75-52-5

nitromethane

A

ammonium formate
540-69-2

ammonium formate

B

water

water

Conditions
ConditionsYield
at 199.9℃; under 13501100 Torr; for 1h; Mechanism; variation of temperature, pressure, time;
ammonium carbonate

ammonium carbonate

calcium diformate
544-17-2

calcium diformate

ammonium formate
540-69-2

ammonium formate

ammonium nitrate

ammonium nitrate

calcium diformate
544-17-2

calcium diformate

ammonium formate
540-69-2

ammonium formate

Conditions
ConditionsYield
dry distn. at 100°C in vacuo;
ammonium nitrate

ammonium nitrate

sodium formate
141-53-7

sodium formate

ammonium formate
540-69-2

ammonium formate

Conditions
ConditionsYield
dry distn. at 100°C in vacuo;
N2-formyl-asparagine
93923-85-4

N2-formyl-asparagine

ammonium formate
540-69-2

ammonium formate

Conditions
ConditionsYield
bei der Destillation im Vakuum; formyl-l-asparagine;
1,3,5-Triazine
290-87-9

1,3,5-Triazine

water
7732-18-5

water

ammonium formate
540-69-2

ammonium formate

methyl thiocyanate
556-64-9

methyl thiocyanate

ammonium hydroxide

ammonium hydroxide

A

Dimethyldisulphide
624-92-0

Dimethyldisulphide

B

ammonium formate
540-69-2

ammonium formate

C

urea
57-13-6

urea

1-amino-2,2,2-trichloro-ethanol
507-47-1

1-amino-2,2,2-trichloro-ethanol

water
7732-18-5

water

A

chloroform
67-66-3

chloroform

B

ammonium formate
540-69-2

ammonium formate

ethyl isothiocyanate
542-90-5

ethyl isothiocyanate

ammonium hydroxide

ammonium hydroxide

A

Diethyl disulfide
110-81-6

Diethyl disulfide

B

ammonium formate
540-69-2

ammonium formate

C

urea
57-13-6

urea

2,2,2-trichloro-4-trichloromethyl-2λ5-[1.3.2]dioxaphosphetane

2,2,2-trichloro-4-trichloromethyl-2λ5-[1.3.2]dioxaphosphetane

ammonia
7664-41-7

ammonia

A

chloroform
67-66-3

chloroform

B

ammonium formate
540-69-2

ammonium formate

C

ammonium phosphate

ammonium phosphate

sodium formate
141-53-7

sodium formate

ammonium carbonate

ammonium carbonate

ammonium formate
540-69-2

ammonium formate

Conditions
ConditionsYield
at 80℃; Destillation im Vakuum bei 100grad;
at 80℃;
carbon monoxide
201230-82-2

carbon monoxide

ammonia
7664-41-7

ammonia

A

ammonium carbonate

ammonium carbonate

B

ammonium formate
540-69-2

ammonium formate

C

ammonium cyanide
71680-52-9, 130166-69-7

ammonium cyanide

Conditions
ConditionsYield
High Pressure; 200°C, 170 atm, catalyst: clay;
3-(amino-oxazol-2-yl-methyl)-pyrrolidine-1-carboxylic acid benzyl ester
852655-84-6

3-(amino-oxazol-2-yl-methyl)-pyrrolidine-1-carboxylic acid benzyl ester

ammonium formate
540-69-2

ammonium formate

C-oxazol-2-yl-C-pyrrolidin-3-yl-methylamine
852655-85-7

C-oxazol-2-yl-C-pyrrolidin-3-yl-methylamine

Conditions
ConditionsYield
palladium 10% on activated carbon In methanol at 65℃; for 2.5h;100%
ammonium formate
540-69-2

ammonium formate

C15H15ClN2
115419-53-9

C15H15ClN2

C16H16N2O2
115419-56-2

C16H16N2O2

Conditions
ConditionsYield
In methanol for 1h; Ambient temperature;98%
ammonium formate
540-69-2

ammonium formate

N,N'-Bis-'D'-5-aminopyrrolidin-2-one
100039-05-2

N,N'-Bis-'D'-5-aminopyrrolidin-2-one

'D'-5-Aminopyrrolidin-2-one Formic Acid Salt
100039-06-3, 100039-08-5

'D'-5-Aminopyrrolidin-2-one Formic Acid Salt

Conditions
ConditionsYield
With hydrogen; palladium In methanol; N,N-dimethyl-formamide for 0.166667h;97%
ammonium formate
540-69-2

ammonium formate

N,N'-Bis-'L'-5-aminopyrrolidin-2-one
66488-70-8

N,N'-Bis-'L'-5-aminopyrrolidin-2-one

'L'-5-Aminopyrrolidin-2-one formic acid salt
100039-06-3

'L'-5-Aminopyrrolidin-2-one formic acid salt

Conditions
ConditionsYield
With hydrogen; palladium In methanol; N,N-dimethyl-formamide for 0.166667h;95%
sodium tetrahydroborate
16940-66-2

sodium tetrahydroborate

ammonium formate
540-69-2

ammonium formate

ammonia borane complex
10043-11-5

ammonia borane complex

Conditions
ConditionsYield
In 1,4-dioxane byproducts: H2, NaO2CH; (inert atmosphere); dioxane added to NaBH4 and NH4O2CH, stirred vigorously at 40°C for ca 2 h; cooled to room temp., filtered, washed (dioxane); the combined filtratesconcd. (vac.); elem. anal.;95%
In tetrahydrofuran (inert atmosphere); at 25-40°C for 2-25 h;93%
In tetrachloromethane (inert atmosphere); at 40°C for 13 h;
ammonium formate
540-69-2

ammonium formate

Z-MePhe-MeA2bu(γPht)-O-tBu

Z-MePhe-MeA2bu(γPht)-O-tBu

MePhe-MeA2bu(γPht)-O-tBu*HCOOH

MePhe-MeA2bu(γPht)-O-tBu*HCOOH

Conditions
ConditionsYield
With hydrogen; palladium on activated charcoal In methanol for 1h; Ambient temperature;92%
ammonium formate
540-69-2

ammonium formate

cyclohexanone
108-94-1

cyclohexanone

cycloheptyl isonitrile
134420-07-8

cycloheptyl isonitrile

1-Formylamino-cyclohexanecarboxylic acid cycloheptylamide
134455-15-5

1-Formylamino-cyclohexanecarboxylic acid cycloheptylamide

Conditions
ConditionsYield
In methanol; water for 1h; Heating;92%
Tetrahydrothiopyran-4-one
1072-72-6

Tetrahydrothiopyran-4-one

ammonium formate
540-69-2

ammonium formate

cycloheptyl isonitrile
134420-07-8

cycloheptyl isonitrile

N-cycloheptyl-4-formylaminotetrahydrothiopyran-4-carboxamide
156490-26-5

N-cycloheptyl-4-formylaminotetrahydrothiopyran-4-carboxamide

Conditions
ConditionsYield
In methanol; water for 1h; Heating;90%
ammonium formate
540-69-2

ammonium formate

PhOCH2CO-Arg(NO2)-Ala-OBzl
92261-85-3

PhOCH2CO-Arg(NO2)-Ala-OBzl

PhO-CH2CO-Arg-Ala*HCOOH

PhO-CH2CO-Arg-Ala*HCOOH

Conditions
ConditionsYield
palladium In methanol; formic acid Ambient temperature;90%
cobalt(II) chloride hexahydrate

cobalt(II) chloride hexahydrate

ammonium formate
540-69-2

ammonium formate

[ammonium][Co(II)(formate)3]

[ammonium][Co(II)(formate)3]

Conditions
ConditionsYield
In methanol MeOH soln. of (NH4)(HCOO) was placed at the bottom of a glass tube and at this soln. MeOH was gently added followed by layering MeOH soln. of Co-contg. compd.; the tube was sealed and kept undisturbed; crystals were harvested after 5 d; crystals were washed with methanol and dried under vac.; elem. anal.;90%
ammonium formate
540-69-2

ammonium formate

1-(3,4-dimethoxyphenyl)-2-(3,4,5-trimethoxyphenyl)ethan-1-one
80235-72-9

1-(3,4-dimethoxyphenyl)-2-(3,4,5-trimethoxyphenyl)ethan-1-one

N-(1-(3,4-dimethoxyphenyl)-2-(3,4,5-trimethoxyphenyl)ethyl)formamide
80235-74-1

N-(1-(3,4-dimethoxyphenyl)-2-(3,4,5-trimethoxyphenyl)ethyl)formamide

Conditions
ConditionsYield
With formic acid; formamide at 185 - 190℃; for 3.5h;88%
ammonium formate
540-69-2

ammonium formate

3-(2-phenyl-5-trifluoromethyloxazol-4-yl)propanol
148183-79-3

3-(2-phenyl-5-trifluoromethyloxazol-4-yl)propanol

Formic acid 3-(2-phenyl-5-trifluoromethyl-oxazol-4-yl)-propyl ester

Formic acid 3-(2-phenyl-5-trifluoromethyl-oxazol-4-yl)-propyl ester

Conditions
ConditionsYield
In xylene for 37h; Heating;86%
ammonium formate
540-69-2

ammonium formate

PhO-CH2CO-D-Arg(NO2)-D-Ala-OBzl
92261-86-4

PhO-CH2CO-D-Arg(NO2)-D-Ala-OBzl

PhO-CH2CO-D-Arg-D-Ala*HCOOH

PhO-CH2CO-D-Arg-D-Ala*HCOOH

Conditions
ConditionsYield
palladium In methanol; formic acid Ambient temperature;85%
p-methoxyphenylisocyanide
10349-38-9

p-methoxyphenylisocyanide

ammonium formate
540-69-2

ammonium formate

cyclohexanone
108-94-1

cyclohexanone

1-Formylamino-cyclohexanecarboxylic acid (4-methoxy-phenyl)-amide
134455-14-4

1-Formylamino-cyclohexanecarboxylic acid (4-methoxy-phenyl)-amide

Conditions
ConditionsYield
In methanol; water for 0.5h; Heating;85%
ammonium oxopentachloromolybdate

ammonium oxopentachloromolybdate

ammonium formate
540-69-2

ammonium formate

triammonium μ-formato-(O,O')-di-μ-oxo-bis(diformato(oxo)molybdate(V))

triammonium μ-formato-(O,O')-di-μ-oxo-bis(diformato(oxo)molybdate(V))

Conditions
ConditionsYield
In ethanol Mo-compound dissolved in ammonium formate soln., mixed with ethanol, set aside for 1 day;; washed with ethanol, reprecipitated, elem. anal.;85%
ammonium formate
540-69-2

ammonium formate

copper(II) bis(trifluoromethanesulfonate)
34946-82-2

copper(II) bis(trifluoromethanesulfonate)

propan-1-ol-3-amine
156-87-6

propan-1-ol-3-amine

(3-aminopropanolato)formatocopper(II)

(3-aminopropanolato)formatocopper(II)

Conditions
ConditionsYield
With C2H5OH In ethanol to soln. of Cu(CF3COO)2 in EtOH was added a soln. of NH2(CH2)3OH in EtOH and a soln. of HCOONH4 in EtOH, kept at room temp. for 1 d; ppt. filtered, washed with EtOH, acetone;85%
ammonium formate
540-69-2

ammonium formate

N-phenylpropionohydrazonoyl chloride
115419-52-8

N-phenylpropionohydrazonoyl chloride

1-formyl-1-phenyl-2-propionylhydrazine
115419-55-1

1-formyl-1-phenyl-2-propionylhydrazine

Conditions
ConditionsYield
In methanol for 0.25h; Ambient temperature;84%
ammonium formate
540-69-2

ammonium formate

C14H21ClN2
115419-54-0

C14H21ClN2

N’-formyl-N’-phenyl-n-caprylhydrazide
115419-58-4

N’-formyl-N’-phenyl-n-caprylhydrazide

Conditions
ConditionsYield
In methanol for 2h; Ambient temperature;84%
Cyclohexyl isocyanide
931-53-3

Cyclohexyl isocyanide

ammonium formate
540-69-2

ammonium formate

cyclohexanone
108-94-1

cyclohexanone

1-Formylamino-cyclohexan-
4507-61-3

1-Formylamino-cyclohexan-

Conditions
ConditionsYield
In methanol; water for 0.5h; Heating;84%
Cyclohexyl isocyanide
931-53-3

Cyclohexyl isocyanide

ammonium formate
540-69-2

ammonium formate

β-naphthaldehyde
66-99-9

β-naphthaldehyde

N-Cyclohexyl-2-formylamino-2-naphthalen-2-yl-acetamide
128243-50-5

N-Cyclohexyl-2-formylamino-2-naphthalen-2-yl-acetamide

Conditions
ConditionsYield
In methanol for 0.5h; Heating;82%
Benzyl isocyanide
88333-03-3, 10340-91-7

Benzyl isocyanide

ammonium formate
540-69-2

ammonium formate

cyclopentanone
120-92-3

cyclopentanone

N-benzyl-1-formamidocyclopentane-1-carboxamide
134420-09-0

N-benzyl-1-formamidocyclopentane-1-carboxamide

Conditions
ConditionsYield
In methanol; water for 1.5h; Heating;82%
Cyclohexyl isocyanide
931-53-3

Cyclohexyl isocyanide

ammonium formate
540-69-2

ammonium formate

1-methylcyclohexan-4-one
589-92-4

1-methylcyclohexan-4-one

1-Formylamino-4-methyl-cyclohexanecarboxylic acid cyclohexylamide
148751-15-9

1-Formylamino-4-methyl-cyclohexanecarboxylic acid cyclohexylamide

Conditions
ConditionsYield
In methanol; water for 1h; Heating;81%

Ammonium formate Consensus Reports

Reported in EPA TSCA Inventory.

Ammonium formate Specification

The Ammonium formate, also known as Formic acid, ammonium salt, is an organic compound with the formula NH4HCO2. It belongs to the product categories of Industrial/Fine Chemicals; Alphabetical Synthetic Reagents; Ammonium Biological Buffers; Biological Buffers; BioUltra Buffers; Buffer Solutions Protein Structural Analysis; Inorganic Salts; Optimization Reagents; X-Ray Crystallography. Its EINECS registry number is 208-753-9. With the CAS registry number 540-69-2, its IUPAC name is azanium formate. It is a colorless, hygroscopic, crystalline solid.

Physical properties of Ammonium formate: (1)H-Bond Donor: 1; (2)H-Bond Acceptor: 2; (3)Rotatable Bond Count: 0; (4)Exact Mass: 63.032028; (5)MonoIsotopic Mass: 63.032028; (6)Topological Polar Surface Area: 41.1; (7)Heavy Atom Count: 4; (8)Formal Charge: 0; (9)Complexity: 7.5; (10)Isotope Atom Count: 0; (11)Defined Atom StereoCenter Count: 0; (12)Undefined Atom StereoCenter Count: 0; (13)Defined Bond StereoCenter Count: 0; (14)Undefined Bond StereoCenter Count: 0; (15)Covalently-Bonded Unit Count: 2.

Preparation of Ammonium formate: this chemical can be prepared by formic acid and NH3 via neutralization reaction. The formic acid and H2O is freezed. The reaction mixture is stirred at -5 °C with the PH value of 7-7.5 and is filtered. Finally, you can get Ammonium formate.

Ammonium formate can be prepared by formic acid and NH3 via neutralization reaction

Uses: formic acid can be obtained by reacting Ammonium formate with a dilute acid, and since ammonium formate is also produced from formic acid, it can serve as a way of storing formic acid. Ammonium formate can also be used in palladium on carbon (Pd/C) reduction of functional groups. Ammonium formate can be used for reductive amination of aldehydes and ketones. Ammonium formate can be used as a buffer in high performance liquid chromatography (HPLC), and is suitable for use with liquid chromatography/mass spectroscopy (LC/MS).

When you are using this chemical, please be cautious about it as the following:
This chemical may cause inflammation to the skin or other mucous membranes. It is irritating to eyes, respiratory system and skin. In case of contact with eyes, you should rinse immediately with plenty of water and seek medical advice. Whenever you will contact it, please wear suitable protective clothing, gloves and eye/face protection.

You can still convert the following datas into molecular structure:
(1)Canonical SMILES: C(=O)[O-].[NH4+]
(2)InChI: InChI=1S/CH2O2.H3N/c2-1-3;/h1H,(H,2,3);1H3
(3)InChIKey: VZTDIZULWFCMLS-UHFFFAOYSA-N

The toxicity data is as follows:

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
mouse LD50 intravenous 410mg/kg (410mg/kg)   Zeitschrift fuer Ernaehrungswissenschaft. Vol. 9, Pg. 332, 1969.
mouse LD50 oral 2250mg/kg (2250mg/kg)   Zeitschrift fuer Ernaehrungswissenschaft. Vol. 9, Pg. 332, 1969.

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