Conditions | Yield |
---|---|
With water In hydrogenchloride Kinetics; at 35 45 and 65°C; | |
With hydrogen bromide In hydrogen bromide Kinetics; | |
explosive decomposition; |
acetylacetaldehyde dimethyl acetal
formamide
A
4-Methylpyrimidine
B
methanol
C
ammonium formate
Conditions | Yield |
---|---|
at 190℃; for 3.5h; | A 79% B n/a C n/a |
Conditions | Yield |
---|---|
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 formate
Conditions | Yield |
---|---|
With water; nickel at 125 - 200℃; under 73550.8 - 330978 Torr; Hydrogenation; |
Conditions | Yield |
---|---|
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; |
ammonium formate
Conditions | Yield |
---|---|
With ammonia; water at 160 - 220℃; under 117681 - 279493 Torr; |
Conditions | Yield |
---|---|
In gas | |
in present of catalysts; | |
With H2 In water |
Conditions | Yield |
---|---|
With H2O In water further products; in alkaline soln.; | |
With H2O In water further products; in alkaline soln.; |
carbon monoxide
ammonium formate
Conditions | Yield |
---|---|
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; |
Conditions | Yield |
---|---|
With water In water | |
With H2O In water |
Conditions | Yield |
---|---|
With H2; catalyst: (RuCl2(benzene))2/dppm In tetrahydrofuran; water 2 h at 70°C at 50 bar H2; detd. by NMR; |
Conditions | Yield |
---|---|
With carbon monoxide In water aq. soln. in sealed tube (130°C); excess of CO;; |
Conditions | Yield |
---|---|
With carbon monoxide In water aq. soln. in sealed tube (130°C);; |
Conditions | Yield |
---|---|
In water Electrolysis; | |
In water Electrolysis; |
Conditions | Yield |
---|---|
With ammonium amalgame | |
With ammonium amalgame |
Conditions | Yield |
---|---|
In water | |
In water |
Conditions | Yield |
---|---|
In neat (no solvent) decomposition at 120°C; further byproducts;; | |
In neat (no solvent) decomposition at 120°C; further byproducts;; |
ammonium formate
Conditions | Yield |
---|---|
In water byproducts: H3PO4; hydrolysis; |
ammonium formate
Conditions | Yield |
---|---|
With air byproducts: H2SO4; hydrolysis; |
Conditions | Yield |
---|---|
With glycerol beim Erhitzen; Nebenprod.2:Ammonium-carbonat; Nebenprod.3:Ammonium-cyanid; |
Conditions | Yield |
---|---|
at 45℃; Kinetics; Hydrolysis; |
Conditions | Yield |
---|---|
With ammonia; water |
Conditions | Yield |
---|---|
With ammonia |
Conditions | Yield |
---|---|
In not given byproducts: NaHCO3; introduction of NH3 and CO2 into technical sodium formate soln.; |
ammonium formate
Conditions | Yield |
---|---|
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; |
Conditions | Yield |
---|---|
saponification of Ba(CN)2 with water; precipitating of Ba with CO2; | |
saponification of Ba(CN)2 with water; precipitating of Ba with CO2; |
Conditions | Yield |
---|---|
at 199.9℃; under 13501100 Torr; for 1h; Mechanism; variation of temperature, pressure, time; |
Conditions | Yield |
---|---|
dry distn. at 100°C in vacuo; |
Conditions | Yield |
---|---|
dry distn. at 100°C in vacuo; |
N2-formyl-asparagine
ammonium formate
Conditions | Yield |
---|---|
bei der Destillation im Vakuum; formyl-l-asparagine; |
methyl thiocyanate
A
Dimethyldisulphide
B
ammonium formate
C
urea
1-amino-2,2,2-trichloro-ethanol
water
A
chloroform
B
ammonium formate
ethyl isothiocyanate
A
Diethyl disulfide
B
ammonium formate
C
urea
Conditions | Yield |
---|---|
at 80℃; Destillation im Vakuum bei 100grad; | |
at 80℃; |
carbon monoxide
ammonia
B
ammonium formate
C
ammonium cyanide
Conditions | Yield |
---|---|
High Pressure; 200°C, 170 atm, catalyst: clay; |
3-(amino-oxazol-2-yl-methyl)-pyrrolidine-1-carboxylic acid benzyl ester
ammonium formate
C-oxazol-2-yl-C-pyrrolidin-3-yl-methylamine
Conditions | Yield |
---|---|
palladium 10% on activated carbon In methanol at 65℃; for 2.5h; | 100% |
Conditions | Yield |
---|---|
In methanol for 1h; Ambient temperature; | 98% |
ammonium formate
N,N'-Bis-'D'-5-aminopyrrolidin-2-one
'D'-5-Aminopyrrolidin-2-one Formic Acid Salt
Conditions | Yield |
---|---|
With hydrogen; palladium In methanol; N,N-dimethyl-formamide for 0.166667h; | 97% |
ammonium formate
N,N'-Bis-'L'-5-aminopyrrolidin-2-one
'L'-5-Aminopyrrolidin-2-one formic acid salt
Conditions | Yield |
---|---|
With hydrogen; palladium In methanol; N,N-dimethyl-formamide for 0.166667h; | 95% |
Conditions | Yield |
---|---|
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; |
Conditions | Yield |
---|---|
With hydrogen; palladium on activated charcoal In methanol for 1h; Ambient temperature; | 92% |
ammonium formate
cyclohexanone
cycloheptyl isonitrile
1-Formylamino-cyclohexanecarboxylic acid cycloheptylamide
Conditions | Yield |
---|---|
In methanol; water for 1h; Heating; | 92% |
Tetrahydrothiopyran-4-one
ammonium formate
cycloheptyl isonitrile
N-cycloheptyl-4-formylaminotetrahydrothiopyran-4-carboxamide
Conditions | Yield |
---|---|
In methanol; water for 1h; Heating; | 90% |
Conditions | Yield |
---|---|
palladium In methanol; formic acid Ambient temperature; | 90% |
Conditions | Yield |
---|---|
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
1-(3,4-dimethoxyphenyl)-2-(3,4,5-trimethoxyphenyl)ethan-1-one
N-(1-(3,4-dimethoxyphenyl)-2-(3,4,5-trimethoxyphenyl)ethyl)formamide
Conditions | Yield |
---|---|
With formic acid; formamide at 185 - 190℃; for 3.5h; | 88% |
ammonium formate
3-(2-phenyl-5-trifluoromethyloxazol-4-yl)propanol
Conditions | Yield |
---|---|
In xylene for 37h; Heating; | 86% |
Conditions | Yield |
---|---|
palladium In methanol; formic acid Ambient temperature; | 85% |
p-methoxyphenylisocyanide
ammonium formate
cyclohexanone
1-Formylamino-cyclohexanecarboxylic acid (4-methoxy-phenyl)-amide
Conditions | Yield |
---|---|
In methanol; water for 0.5h; Heating; | 85% |
ammonium formate
Conditions | Yield |
---|---|
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
copper(II) bis(trifluoromethanesulfonate)
propan-1-ol-3-amine
Conditions | Yield |
---|---|
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
N-phenylpropionohydrazonoyl chloride
1-formyl-1-phenyl-2-propionylhydrazine
Conditions | Yield |
---|---|
In methanol for 0.25h; Ambient temperature; | 84% |
Conditions | Yield |
---|---|
In methanol for 2h; Ambient temperature; | 84% |
Cyclohexyl isocyanide
ammonium formate
cyclohexanone
1-Formylamino-cyclohexan-
Conditions | Yield |
---|---|
In methanol; water for 0.5h; Heating; | 84% |
Cyclohexyl isocyanide
ammonium formate
β-naphthaldehyde
N-Cyclohexyl-2-formylamino-2-naphthalen-2-yl-acetamide
Conditions | Yield |
---|---|
In methanol for 0.5h; Heating; | 82% |
Benzyl isocyanide
ammonium formate
cyclopentanone
N-benzyl-1-formamidocyclopentane-1-carboxamide
Conditions | Yield |
---|---|
In methanol; water for 1.5h; Heating; | 82% |
Cyclohexyl isocyanide
ammonium formate
1-methylcyclohexan-4-one
1-Formylamino-4-methyl-cyclohexanecarboxylic acid cyclohexylamide
Conditions | Yield |
---|---|
In methanol; water for 1h; Heating; | 81% |
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.
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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