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506-87-6 Usage

Outline

Ammonium carbonate is positive ammonium salt of carbonic acid normal salt, the formula is (NH4)2CO3. Pure product is colorless or white cubic crystal or powder, it has strong smell of ammonia. Industrial product is complex salt of ammonium bicarbonate and ammonium carbamate, it is white, flaky or small block of solid product crushed form. It is often with a molecular crystal water, it is hygroscopic, soluble in water, it can decompose in case of hot water. It is insoluble in ethanol and carbon disulfide. Ammonium carbonate can rapidly decompose into ammonia, carbon dioxide and water at 58℃. Ammonium carbonate can be obtained by ammonia introduces into solution of sodium carbonate with half times, the solution crystallizes at 30°C. It gradually loses ammonia to form ammonium bicarbonate in air.

Solubility in water (g/100ml)

The grams which dissolve per 100 ml of water:100g/20 ℃.

Related reactions of the formula

At room temperature for significant decomposition: (NH4) 2CO3 → 2NH3 + CO2 + H2O At low temperature and a certain pressure, carbon dioxide and water with an excess of ammonia, ammonium carbonate can be obtained: 2NH3 + CO2 + H2O → (NH4) 2CO3 Ammonium sulfate and calcium carbonate suspension under heating to generate ammonium carbonate: (NH4) 2SO4 + CaCO3 → (NH4) 2CO3 + CaSO4 Urea in aqueous solution will gradually react with water to form ammonium carbonate: CO (NH2) 2 + 2H2O → (NH4) 2CO3

Toxcity

If it splashes into the eye accidentally, rinse immediately with plenty of water. It has stimulating effect on the skin. It should pay attention to dust prevention and dust extraction, respiratory protection, skin protection.

Chemical properties

It is matte orthorhombic crystalline powder. It has strong ammonia odor. It usually can not get anhydrous salt, industrial salt is actually a complex of ammonium bicarbonate and ammonium carbamate. The amount of ammonia is 31%, The amount of carbon dioxide is 56%. It is soluble in water, insoluble in ethanol, carbon disulfide, and concentrated ammonia. It is unstable in the air, it will gradually become ammonium bicarbonate and ammonium carbamate. When be dried at 58℃, it can easily decompose, release ammonia and carbon dioxide. Aqueous solution begins to decompose at 70℃. It is unstable for light and heat. It has slightly hygroscopic.

Uses

Different sources of media describe the Uses of 506-87-6 differently. You can refer to the following data:
1. It is used as raw material for baking powder, various ammonium salts, buffer agent, auxiliaries, fertilizer and analytical reagent. Edible ammonium carbonate is used as buffer, neutralizing agent, leavening agent, fermentation promoter (manufacture of wine). It is used for fire fighting, detergents, and used in medicine, rubber, and other industrial fermentation. The above information is edited by the lookchem of Wang Xiaodong.
2. Ammonium Carbonate is a dough strengthener, a leavening agent, a ph control agent, and a texturizer. it is prepared by the sublima- tion of a mixture of ammonium sulfate and calcium carbonate, and occurs as a white powder or a hard, white translucent mass.
3. Pharmaceutic aid (source of ammonia).
4. Ammonium carbonate is widely utilized as a leavening agent in lebkuchen, cookies and flat biscuits. It finds an important application as an emetic and an active ingredient in some cough syrups. It is the main component in smelling salts and an active ingredient in some smokeless tobacco products, shampoos and dyes used in textile industries. It is an important predecessor to the modern leavening agent?s baking soda and baking powder. It serves as a foaming agent for the production of expanded material. It is also used as a reagent for analytical purposes in the chemical industry.

Production method

Carbonization method: Carbon dioxide, ammonia and steam synthesized directly sodium carbonate, it passes through the cooling chamber, uses water to direct cooling, and then it is refined to obtain ammonium carbonate products. 2NH3 + CO2 + H2O → (NH4) 2CO3

Category

Toxic substances.

Toxicity grading

highly toxic.

Acute toxicity

Intravenous-Mouse LD50: 96 mg/kg; Intravenous-Dogs LDL0: 200 mg/kg.

Flammability hazard characteristics

It can produce toxic fumes of nitrogen oxides and ammonia at high temperature.

Extinguishing agent

Dry powder, foam, sand, carbon dioxide, water mist.

Chemical Properties

Different sources of media describe the Chemical Properties of 506-87-6 differently. You can refer to the following data:
1. Anunonium carbonate is a white water-soluble, volatile solid prepared by reaction of NH4OH and CO2 and crystallizing from dilute alcohol. Ammonium carbonate loses NH3,CO2, and H20 at ordinary temperatures, and rapidly at 58°C.
2. Ammonium carbonate is a colorless crystal or white lumpy powder with a strong ammonia odor. The odor specific gravity (gas)52.7; Threshold is ,5 ppm as ammonia gas.

Physical properties

Colorless or translucent hard crystalline mass or white cubic crystals or powder; sharp taste; odor of ammonia; decomposes at 58°C; slow decomposition at ambient temperatures; readily dissolves in cold water; decomposes in hot water; insoluble in liquid ammonia, alcohol and carbon disulfide.

Definition

Different sources of media describe the Definition of 506-87-6 differently. You can refer to the following data:
1. ammonium carbonate: A colourlessor white crystalline solid,(NH4)2CO3, usually encountered asthe monohydrate. It is very soluble incold water. The compound decomposesslowly to give ammonia, water,and carbon dioxide. Commercial ‘ammoniumcarbonate’ is a double saltof ammonium hydrogencarbonateand ammonium aminomethanoate(carbamate), NH4HCO3.NH2COONH4.This material is manufactured byheating a mixture of ammoniumchloride and calcium carbonate andrecovering the product as a sublimedsolid. It readily releases ammoniaand is the basis of sal volatile. It isalso used in dyeing and wool preparationand in baking powders.
2. A mixture of ammonium acid carbonate and ammo- nium carbamate.

Preparation

Ammonium carbonate is obtained by passing carbon dioxide into aqueous ammonia solution in a column or tower. Ammonia, carbon dioxide and water vapor are distilled and the vapors condensed into a solid crystalline mass. It also may be prepared by subliming a mixture of ammonium sulfate and calcium carbonate.

General Description

A colorless crystalline solid or a white powder with a strong odor of ammonia. Noncombustible. The primary hazard is the threat to the environment. Immediate steps should be taken to limit spread to the environment. Used to make other ammonium compounds, in pharmaceuticals, in food processing.

Air & Water Reactions

Water soluble.

Reactivity Profile

Ammonium carbonate decomposes when heated to give gaseous ammonia and gaseous carbon dioxide. Reaction is non-explosvie. Causes decomposition of sodium hypochlorite within a few seconds [Mellor 2 Supp. 1:550 1956].

Hazard

Evolves irritating fumes when heated.

Health Hazard

Inhalation causes irritation of nose and throat. Ingestion may cause gastric irritation. Contact with eyes or skin causes irritation.

Agricultural Uses

Ammonium carbonate, (NH4)2CO3, is an intermediate product formed during the synthesis of urea. Ammonium carbonate on decomposition yields urea and water.

Safety Profile

Poison by subcutaneous and intravenous routes. When heated to decomposition it emits toxic fumes of NO, and NH3.

Potential Exposure

It is used in dyeing, tanning, medicines, fire extinguishers; to make casein glue; ammonia salts; and baking powders. A laboratory reagent.

Shipping

UN3077 Environmentally hazardous substances, solid, n.o.s., Hazard class: 9; Labels: 9-Miscellaneous hazardous material, Technical Name Required.

Incompatibilities

Acids, acid salts; salts of iron and zinc, alkaloids, calomel and tartar emetic. Keep cool, below 38 C. Contact with inorganic acids may form CO2, heat, and dangerous spattering.

Waste Disposal

Slowly deposit in a large container of water. Add excess amounts of soda ash and let stand for 24 hours. Decant to another container, neutralize with hydrochloric acid, and drain with an excess of water. Ship to landfill.

Check Digit Verification of cas no

The CAS Registry Mumber 506-87-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,0 and 6 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 506-87:
(5*5)+(4*0)+(3*6)+(2*8)+(1*7)=66
66 % 10 = 6
So 506-87-6 is a valid CAS Registry Number.
InChI:InChI=1/CH2O3.2H3N/c2-1(3)4;;/h(H2,2,3,4);2*1H3

506-87-6 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (12980)  Ammonium carbonate, Puratronic?, 99.999% (metals basis)   

  • 506-87-6

  • 10g

  • 381.0CNY

  • Detail
  • Alfa Aesar

  • (12980)  Ammonium carbonate, Puratronic?, 99.999% (metals basis)   

  • 506-87-6

  • 50g

  • 1269.0CNY

  • Detail
  • Alfa Aesar

  • (12980)  Ammonium carbonate, Puratronic?, 99.999% (metals basis)   

  • 506-87-6

  • 250g

  • 3889.0CNY

  • Detail
  • Alfa Aesar

  • (36229)  Ammonium carbonate, ACS, NH3 30.0+%   

  • 506-87-6

  • 500g

  • 406.0CNY

  • Detail
  • Alfa Aesar

  • (36229)  Ammonium carbonate, ACS, NH3 30.0+%   

  • 506-87-6

  • 2kg

  • 1413.0CNY

  • Detail
  • Alfa Aesar

  • (A13955)  Ammonium carbonate, NH3 ca 30%   

  • 506-87-6

  • 1000g

  • 177.0CNY

  • Detail
  • Alfa Aesar

  • (A13955)  Ammonium carbonate, NH3 ca 30%   

  • 506-87-6

  • 5000g

  • 741.0CNY

  • Detail
  • Sigma-Aldrich

  • (207861)  Ammoniumcarbonate  ACS reagent, ≥30.0% NH3 basis

  • 506-87-6

  • 207861-25G

  • 232.83CNY

  • Detail
  • Sigma-Aldrich

  • (207861)  Ammoniumcarbonate  ACS reagent, ≥30.0% NH3 basis

  • 506-87-6

  • 207861-100G

  • 469.17CNY

  • Detail
  • Sigma-Aldrich

  • (207861)  Ammoniumcarbonate  ACS reagent, ≥30.0% NH3 basis

  • 506-87-6

  • 207861-500G

  • 718.38CNY

  • Detail
  • Sigma-Aldrich

  • (207861)  Ammoniumcarbonate  ACS reagent, ≥30.0% NH3 basis

  • 506-87-6

  • 207861-1KG

  • 1,364.22CNY

  • Detail
  • Sigma-Aldrich

  • (207861)  Ammoniumcarbonate  ACS reagent, ≥30.0% NH3 basis

  • 506-87-6

  • 207861-2.5KG

  • 2,871.18CNY

  • Detail

506-87-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name Ammonium carbonate

1.2 Other means of identification

Product number -
Other names hartshorn

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Specialized Industrial Chemicals
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:506-87-6 SDS

506-87-6Synthetic route

bis(guanidinium)bis(oxalato)cuprate(II)

bis(guanidinium)bis(oxalato)cuprate(II)

ammonium carbonate
506-87-6

ammonium carbonate

Conditions
ConditionsYield
at 250 - 310℃; Inert atmosphere;
carbon dioxide
124-38-9

carbon dioxide

ammonia
7664-41-7

ammonia

ammonium carbonate
506-87-6

ammonium carbonate

thiourea
17356-08-0

thiourea

A

carbon dioxide
124-38-9

carbon dioxide

B

ammonium carbonate
506-87-6

ammonium carbonate

C

S, HI, I2, (NH4)2SO4

S, HI, I2, (NH4)2SO4

Conditions
ConditionsYield
With iodic acid In water at 25℃; for 0.666667h; Rate constant; Product distribution; Mechanism; different ratios of HIO3, reagent and reaction times;
ammonium carbonate
506-87-6

ammonium carbonate

(+/-)-1-(N-tert-Butoxycarbonylamino)propan-2-one
170384-29-9

(+/-)-1-(N-tert-Butoxycarbonylamino)propan-2-one

rac-tert-butyl <(4-methyl-2,5-dioxoimidazolidin-4-yl)methyl>carbamate

rac-tert-butyl <(4-methyl-2,5-dioxoimidazolidin-4-yl)methyl>carbamate

Conditions
ConditionsYield
With potassium cyanide In ethanol at 50℃; for 20h;100%
4-cyanophenyl methyl ketone
1443-80-7

4-cyanophenyl methyl ketone

potassium cyanide
151-50-8

potassium cyanide

ammonium carbonate
506-87-6

ammonium carbonate

4-(R,S)-(4-cyanophenyl)-4-methyl-2,5-dioxoimidazolidine
169808-00-8

4-(R,S)-(4-cyanophenyl)-4-methyl-2,5-dioxoimidazolidine

Conditions
ConditionsYield
In ethanol at 60℃; for 72h;100%
2-(tritylamino)methyl-5,6-dihydro-2H-pyran-3(4H)-one
1037368-71-0

2-(tritylamino)methyl-5,6-dihydro-2H-pyran-3(4H)-one

sodium cyanide
143-33-9

sodium cyanide

ammonium carbonate
506-87-6

ammonium carbonate

6-(tritylamino)methyl-7-oxa-1,3-diazaspiro [4.5]decane-2,4-dione
1037368-72-1

6-(tritylamino)methyl-7-oxa-1,3-diazaspiro [4.5]decane-2,4-dione

Conditions
ConditionsYield
With ammonia; water; ammonium chloride In ethanol at 60℃; for 23h;100%
potassium cyanide

potassium cyanide

spiro<3.3>heptane-2,6-dione
20061-23-8

spiro<3.3>heptane-2,6-dione

ammonium carbonate
506-87-6

ammonium carbonate

C11H12N4O4
1196087-88-3

C11H12N4O4

Conditions
ConditionsYield
Stage #1: potassium cyanide; spiro<3.3>heptane-2,6-dione; ammonium carbonate In ethanol; water at 60℃; for 75h; Bucherer-Bergs reaction; Inert atmosphere;
Stage #2: With hydrogenchloride; water In ethanol for 1h; pH=2; Inert atmosphere; Cooling with ice;
100%
potassium cyanide

potassium cyanide

8-methoxy-2-tetralone
5309-19-3

8-methoxy-2-tetralone

ammonium carbonate
506-87-6

ammonium carbonate

3',4'-dihydro-8'-methoxyspiro2,5-dione
67544-72-3

3',4'-dihydro-8'-methoxyspiro2,5-dione

Conditions
ConditionsYield
With water In ethanol at 80℃; for 12h; Product distribution / selectivity; Sealed tube;100%
In ethanol; water at 80℃; for 12h;100%
potassium cyanide

potassium cyanide

1-phenylmethyl-4-piperidone
3612-20-2

1-phenylmethyl-4-piperidone

ammonium carbonate
506-87-6

ammonium carbonate

8-benzyl-1,3,8-triaza-spiro[4.5]decane-2,4-dione
28936-94-9

8-benzyl-1,3,8-triaza-spiro[4.5]decane-2,4-dione

Conditions
ConditionsYield
Stage #1: 1-phenylmethyl-4-piperidone; ammonium carbonate In methanol; water Cooling with ice;
Stage #2: potassium cyanide With water In methanol at 20℃; for 72h; Cooling with ice;
100%
cyclohexanedione monoethylene ketal
4746-97-8

cyclohexanedione monoethylene ketal

potassium cyanide
151-50-8

potassium cyanide

ammonium carbonate
506-87-6

ammonium carbonate

9,12-dioxa-2,4-diazadispiro[4.2.4Λ{8}.2Λ{5}]tetradecane-1,3-dione
54621-17-9

9,12-dioxa-2,4-diazadispiro[4.2.4Λ{8}.2Λ{5}]tetradecane-1,3-dione

Conditions
ConditionsYield
In ethanol; water at 65℃; for 24h; Bucherer-Bergs reaction;98%
With water In methanol at 65℃; for 18h;68%
2,3-dihydro-4H-[1]benzothiopyran-4-one
3528-17-4

2,3-dihydro-4H-[1]benzothiopyran-4-one

potassium cyanide
151-50-8

potassium cyanide

ammonium carbonate
506-87-6

ammonium carbonate

spiro(hydantoin-5,4'-thiochromane)
66892-42-0

spiro(hydantoin-5,4'-thiochromane)

Conditions
ConditionsYield
In ethanol; water at 55 - 60℃; Bucherer-Bergs reaction;98%
sodium cyanide
773837-37-9

sodium cyanide

ammonium carbonate
506-87-6

ammonium carbonate

1,2,3,4-tetrahydronaphthalen-2-one
530-93-8

1,2,3,4-tetrahydronaphthalen-2-one

7,8-benzo-1,3-diazasprio[4.5]decane-2,4-dione
52094-70-9

7,8-benzo-1,3-diazasprio[4.5]decane-2,4-dione

Conditions
ConditionsYield
In ethanol; water at 80℃; for 48h;98%
1-Methyl-4-piperidone
1445-73-4

1-Methyl-4-piperidone

potassium cyanide

potassium cyanide

ammonium carbonate
506-87-6

ammonium carbonate

8-methyl-1,3,8-triazaspiro<4.5>decane-2,4-dione
52094-69-6

8-methyl-1,3,8-triazaspiro<4.5>decane-2,4-dione

Conditions
ConditionsYield
In methanol; water at 90℃; for 0.166667h; Bucherer-Bergs Reaction; Sealed tube; Microwave irradiation;98%
In methanol; water at 23℃; for 48h;51%
potassium cyanide

potassium cyanide

(1S,5S,6S)-6-(diisopropoxyphosphoryl)bicyclo[3.1.0]hexan-2-one
1246564-33-9

(1S,5S,6S)-6-(diisopropoxyphosphoryl)bicyclo[3.1.0]hexan-2-one

ammonium carbonate
506-87-6

ammonium carbonate

6-(diisopropoxyphosphoryl)-2-spirohydantoinbicyclo-[3.1.0]hexane
1246564-34-0

6-(diisopropoxyphosphoryl)-2-spirohydantoinbicyclo-[3.1.0]hexane

Conditions
ConditionsYield
In ethanol; water at 35℃; for 72h; Bucherer-Bergs reaction; diastereoselective reaction;98%
potassium cyanide

potassium cyanide

4-Phenyl-2-butanone
2550-26-7

4-Phenyl-2-butanone

ammonium carbonate
506-87-6

ammonium carbonate

5-methyl-5-phenethyl-imidazolidine-2,4-dione
5472-90-2, 142777-72-8

5-methyl-5-phenethyl-imidazolidine-2,4-dione

Conditions
ConditionsYield
In ethanol; water at 20℃; for 24h; Temperature; Bucherer-Bergs Reaction; chemoselective reaction;98%
ammonium carbonate
506-87-6

ammonium carbonate

9-cyano-9-amino-1-phenyl-1,3-diazahomoadamantane
147084-84-2

9-cyano-9-amino-1-phenyl-1,3-diazahomoadamantane

1-phenyl-3,6-diazahomoadamantane-9-spiro-5'-imidazolidine-2,4-dione

1-phenyl-3,6-diazahomoadamantane-9-spiro-5'-imidazolidine-2,4-dione

Conditions
ConditionsYield
In ethanol; water 1.) from 55 deg C to 65 deg C, 10 h, 2.) reflux, 1 h;97%
potassium cyanide
151-50-8

potassium cyanide

ammonium carbonate
506-87-6

ammonium carbonate

1-(1H-Indol-3-yl)-cyclobutanecarbaldehyde
218772-68-0

1-(1H-Indol-3-yl)-cyclobutanecarbaldehyde

5-[1-(1H-Indol-3-yl)-cyclobutyl]-imidazolidine-2,4-dione
218772-72-6

5-[1-(1H-Indol-3-yl)-cyclobutyl]-imidazolidine-2,4-dione

Conditions
ConditionsYield
In ethanol; water at 80℃;97%
In ethanol; water at 80℃;63%
ammonium carbonate
506-87-6

ammonium carbonate

3-amino-3 C-cyano-3-deoxy-1,2:5,6-di-O-isopropylidene-α-D-allofuranose
52340-61-1

3-amino-3 C-cyano-3-deoxy-1,2:5,6-di-O-isopropylidene-α-D-allofuranose

1,2:5,6-di-O-isopropylidenespiro[3-deoxy-α-D-ribohexofuranose-3,5'-imidazolidine]-2',4'-dione
330196-69-5

1,2:5,6-di-O-isopropylidenespiro[3-deoxy-α-D-ribohexofuranose-3,5'-imidazolidine]-2',4'-dione

Conditions
ConditionsYield
In methanol; water at 70℃; for 2h;97%
In methanol; water at 70℃; for 4h;80%
potassium cyanide
151-50-8

potassium cyanide

ammonium carbonate
506-87-6

ammonium carbonate

1,2,3,4-tetrahydronaphthalen-2-one
530-93-8

1,2,3,4-tetrahydronaphthalen-2-one

7,8-benzo-1,3-diazasprio[4.5]decane-2,4-dione
52094-70-9

7,8-benzo-1,3-diazasprio[4.5]decane-2,4-dione

Conditions
ConditionsYield
In ethanol; water at 55 - 60℃; Bucherer-Bergs reaction;97%
potassium cyanide

potassium cyanide

7-bromo-2-methyl-3,4-dihydronaphthalen-1(2H)-one
32281-99-5

7-bromo-2-methyl-3,4-dihydronaphthalen-1(2H)-one

ammonium carbonate
506-87-6

ammonium carbonate

7'-bromo-2'-methyl-3',4'-dihydro-2'H-spiro[imidazolidine-4,1'-naphthalene]-2,5-dione
1338093-84-7

7'-bromo-2'-methyl-3',4'-dihydro-2'H-spiro[imidazolidine-4,1'-naphthalene]-2,5-dione

Conditions
ConditionsYield
Stage #1: potassium cyanide; 7-bromo-2-methyl-3,4-dihydronaphthalen-1(2H)-one; ammonium carbonate With sodium hydrogensulfite In ethanol at 130℃;
Stage #2: With hydrogenchloride In ethanol; water pH=~ 3; Cooling with ice;
97%
potassium cyanide

potassium cyanide

pentanal
110-62-3

pentanal

ammonium carbonate
506-87-6

ammonium carbonate

5-n-butylimidazolidine-2,4-dione
102716-78-9

5-n-butylimidazolidine-2,4-dione

Conditions
ConditionsYield
With iron(III) oxide In neat (no solvent) at 70℃; for 0.233333h; Bucherer-Bergs Reaction;97%
potassium cyanide

potassium cyanide

ammonium carbonate
506-87-6

ammonium carbonate

3-Methylacetophenone
585-74-0

3-Methylacetophenone

5-methyl-5-(3-methylphenyl)imidazolidine-2,4-dione
652992-46-6

5-methyl-5-(3-methylphenyl)imidazolidine-2,4-dione

Conditions
ConditionsYield
With iron(III) oxide In neat (no solvent) at 70℃; for 0.55h; Bucherer-Bergs Reaction;97%
In ethanol; water for 0.15h; Time; Bucherer-Bergs Reaction; Microwave irradiation;97%
potassium cyanide

potassium cyanide

2'-Fluoroacetophenone
445-27-2

2'-Fluoroacetophenone

ammonium carbonate
506-87-6

ammonium carbonate

(RS)-5-(2-fluoro-phenyl)-5-methyl-imidazolidine-2,4-dione
7248-25-1

(RS)-5-(2-fluoro-phenyl)-5-methyl-imidazolidine-2,4-dione

Conditions
ConditionsYield
With ammonium hydroxide In ethanol; water at 60℃; for 5.5h;97%
With ammonium hydroxide In ethanol; water at 60℃; for 5.5h;97%
In ethanol at 50℃; for 24h; Bucherer-Bergs Reaction;
potassium cyanide

potassium cyanide

5-(3-hydroxypyrrolidin-1-yl)-2,3-dihydroinden-1-one

5-(3-hydroxypyrrolidin-1-yl)-2,3-dihydroinden-1-one

ammonium carbonate
506-87-6

ammonium carbonate

5'-(3-hydroxypyrrolidin-1-yl)-2',3'-dihydrospiro[imidazolidine-4,1'-indene]-2,5-dione

5'-(3-hydroxypyrrolidin-1-yl)-2',3'-dihydrospiro[imidazolidine-4,1'-indene]-2,5-dione

Conditions
ConditionsYield
With carbamic Acid at 150℃; for 3h;97%

506-87-6Relevant articles and documents

Two novel organic-inorganic hybrid compounds with straight and zigzag chain alignments of Cu(II) centers: Synthesis, crystal structure, spectroscopy, thermal analysis and magnetism

Nenwa, Justin,Djomo, Edith D.,Nfor, Emmanuel N.,Djonwouo, Patrick L.,Mbarki, Mohammed,Fokwa, Boniface P.T.

, p. 26 - 33 (2015/07/15)

Abstract Two hybrid salts, viz. bis(guanidinium) bis(oxalato)cuprate(II) (1) and bis(2-aminopyridinium) bis(oxalato)cuprate(II) trihydrate (2) have been synthesized and characterized by elemental and thermal analyses, IR spectroscopy, single-crystal X-ray diffraction and SQUID magnetometry. Compounds 1 and 2 crystallize in the monoclinic P21/c and triclinic P1ˉ space groups, respectively. In both structures, the four-coordinated Cu(II) ion in [Cu(C2O4)2]2- unit weakly interacts with two axial O-atoms of neighboring units to build a prolate CuO6 octahedron, with regular axial Cu-O bonds of 2.825 ? in 1, whereas in 2 two different Cu-O bonds (2.814 ? and 2.701 ?) are found. In 1, stacking of [Cu(C2O4)2]2- units across internal symmetry-related O-atoms results in equidistantly spaced monomers, thus forming straight Cu(II) chains with regular spacing of Cu?Cu = 3.582 ?. By contrast, in 2, stacking of the [Cu(C2O4)2]2- entities occurs via external symmetry-related O-atoms, yielding zigzag Cu(II) chains with shorter intra-dimer spacing of [Cu?Cu]intra = 3.430 ? and longer inter-dimer spacing of [Cu?Cu]inter = 4.961 ?. The anhydrated compound 1 is stable up to 250 °C, whereas the hydrated compound 2 shows a significant weight loss of solvent water molecules at about 70°C, followed by the decomposition of the network. The magnetic measurements in the 2-300 K temperature range revealed weak antiferromagnetic coupling in the two hybrid salts.

Oxidation of Thiourea by Iodate: a New Type of Oligo-oscillatory Reaction

Rabai, Gyula,Beck, Mihaly T.

, p. 1669 - 1672 (2007/10/02)

In the oxidation of thiourea by iodate in weakly acidic solution the concentration of iodide may exhibit several extrema.The number of extrema mainly depends on the initial ratio of the concentrations of thiourea and iodate, and is at most four. the first step of the reaction results in the formation of iodide which then reacts with iodate to give iodine.The latter oxidizes thiourea in several steps, the end products being sulphate ions, ammonium ions, and carbon dioxide.Taking into account the independently determined rate constants for the sub-systems, the change in the concentrations of iodide and iodine with time can be calculated.There is good agreement between the experimental and theoretical curves.

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