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1336-21-6

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1336-21-6 Usage

Chemical Description

Ammonium hydroxide is a solution of ammonia in water that is used in cleaning products.

Description

Ammonium hydroxide is a colorless, liquid solution with a characteristic and pungent odor. It is ammonia combined with water. Ammonia (NH3) is a compound consisting of nitrogen and hydrogen. Both ammonia and ammonium hydroxide are very common compounds, found naturally in the environment (in air, water, and soil) and in all plants and animals, including humans. Ammonia is a source of nitrogen, an essential element for plants and animals. Ammonia is also produced by the human body – by our organs and tissues and by beneficial bacteria living in our intestines. Ammonia plays an important role in protein synthesis in the human body. In brief summary, all living things need proteins, which are comprised of some 20 different amino acids. While plants and microorganisms can synthesize most amino acids from the nitrogen in the atmosphere, animals cannot. For humans, some amino acids cannot be synthesized at all and must be consumed as intact amino acids. Other amino acids, however, can be synthesized by microorganisms in the gastrointestinal tract with the help of ammonia ions. Thus, ammonia is a key player in the nitrogen cycle and in protein synthesis. Ammonia also helps maintain the body's pH balance.

Chemical Properties

Ammonium hydroxide exists only in the form of an aqueous solution. The compound is prepared by dissolving NH3 in H2O and usually is referred to in industrial trade as aqua ammonia. For industrial procurements, the concentration of NH3 in solution is normally specified in terms of the specific gravity (degrees Baum′e, °Be). Common concentrations are 20 °Be and 26 °Be. The former is equivalent to a sp gr of 0.933, or a concentration of about 17.8% NH3 in solution; the latter is equivalent to a sp gr of 0.897, or a concentration of about 29.4% NH3. These figures apply at a temperature of 60 °F (15.6 °C). Reagent grade NH4OH usually contains approximately 58% NH4OH (from 28 to 30% NH3 in solution).

Uses

Different sources of media describe the Uses of 1336-21-6 differently. You can refer to the following data:
1. Ammonium hydroxide is widely utilized as a leavening agent or acidity regulator in food production. It serves as a precursor to some alkyl amines and is also used in the tobacco industry for flavor enhancement and as a processing aid. During furniture making, it combines with tannic acid and is used to darken or stain wood by making it iron salts. In chemical laboratories, it used for qualitative inorganic analysis, as a complexant and as a base. It is used to clean gold, silve, and platinum jewelry. It is an active component of Tollens' reagent (consisting of a solution of silver nitrate and ammonia) and is used to determine the presence of aldehyde or alpha-hydroxy ketone functional groups.
2. Ammonium Hydroxide is an alkaline that is a clear, colorless solu- tion of ammonia which is used as a leavening agent, a ph control agent, and a surface finishing agent. it is used in baked goods, cheese, puddings, processed fruits, and in the production of caramels.
3. Ammonium hydroxide is used as a cleaning agent and sanitizer in many household and industrial cleaners. Ammonium hydroxide is also used in the manufacture of products such as fertilizer, plastic, rayon and rubber. Aqueous ammonia is corrosive to aluminum alloys, copper, copper alloys, and galvanized surfaces. Aqueous ammonia is an excellent acid neutralizer.

Definition

Ammonium hydroxide,NH40H, is a hydrate of anunonia and exists in crystalline form at -79°C. Normally, it is only found in an aqueous solution also known as aquaanunonia and anunonia water. It is prepared by dissolving NH3 inH20. Reagent grade anunonium hydroxide contains from 28 to 30% NH3 at 15.6 °C. Industrial sales specify the concentration of NH3 in solution in terms of specific gravity. Common concentrations are 20 °Be, which would bea concentration of 17.8% NH3 (specific gravity 0.933) and 26 °Be (specific gravity 0.897), or a concentration of 29.4% NH3. Ammonium hydroxide is an excellent medium for the reaction of NH3 (which becomes the NH4 radical in solution) with other compounds for the preparation of anunonium salts and other nitrogen-containing chemicals. It is an ingredientin deodorants, etching compounds, and cleaning and bleaching materials. Ammoniumhydroxide, as aqua ammonia, finds wide use as a neutralizing agent,because it is inexpensive and strongly alkaline.

Application

▼▲ Industry Application Role/benefit Food processing Baked goods, cheeses, chocolates, other confectionery (e.g., caramel), and puddings Leavening agent, pH control agent and surface-finishing agent/safe and weakly alkaline Meat products Antimicrobial agent/ lowers the acidity of meet, making it difficult for pathogens to survive Cleaning Household and industrial cleansers Cleansing ingredient/ helps to kill microbial agents like bacteria Alkaline disinfectant Main ingredient/disinfects sarin Agriculture Manufacture of fertilizers Source of nitrogen Chemical manufacture Manufacture of alkyl amine Precursor/source of amino Cosmetics Hair dyes and colors pH adjusters/alkaline and safe Chemical analysis Determination of certain elements such as copper and nickel Precipitant/ helps to precipitate various elements Organic synthesis Amide coupling reactions Reagent/source of NH3 SNAr reactions Nucleophile Catalytic reduction of nitriles Additive Others Wood staining Stain agent/better for the wood containing tannic acids Circuit board manufacturing Etching agent/has high alkalinity which makes it very corrosive to certain metals Tobacco processing Processing aid/enhances tobacco flavor Treatment of straw for cattle Produce "ammoniated straw" which is more edible for cattle Coagulation of natural rubber latex pH adjusters/helps to stabilize the natural rubber lattices

General Description

Ammonium hydroxide is a colorless aqueous solution. Concentration of ammonia ranges up to approximately 30%. Ammonia vapors (which arise from the solution) irritate the eyes.

Air & Water Reactions

Water soluble. Generates a small amount of heat when diluted with water.

Reactivity Profile

Ammonium hydroxide reacts exothermically with acids. Evolves toxic gaseous ammonia with strong bases. Reacts extremely violently with dimethyl sulfate [NFPA 491M 1991]. Reacts with aqueous silver nitrate sodium hydroxide to give a black precipitate of silver nitride. Such a precipitate can explode on stirring [MCA Case History 1554 1968]. Aqueous ammonia and Hg react to form an explosive solid, likely a fulminate. (Thodos, G. Amer. Inst. Chen. Engrs. J., 1964, 10, 274.).

Hazard

Liquid and vapor extremely irritating, especially to eyes.

Health Hazard

Ammonium hydroxide solutions are alkaline solutions, meaning they have high pH level. As a result, ammonium hydroxide is a severe eye, skin, and respiratory tract irritant, and readily burns tissue with which it comes in contact. Splashes to the eye may be serious, as contact may cause severe burns, irritation pain and possibly blindness. Direct contact with skin may cause severe burns if the chemical is not quickly rinsed away with copious amounts of water. Inhaling mists of ammonium hydroxide may result in irritation of the nose and throat with symptoms including burning, coughing, choking and pain. Inhaling concentrated mist may result in pulmonary edema and shock. Ingesting ammonium hydroxide may cause pain and burns of the esophagus and gastrointestinal tract. TOXIC; inhalation, ingestion or skin contact with material may cause severe injury or death. Contact with molten substance may cause severe burns to skin and eyes. Avoid any skin contact. Effects of contact or inhalation may be delayed. Fire may produce irritating, corrosive and/or toxic gases. Runoff from fire control or dilution water may be corrosive and/or toxic and cause pollution.

Fire Hazard

Non-combustible, substance itself does not burn but may decompose upon heating to produce corrosive and/or toxic fumes. Some are oxidizers and may ignite combustibles (wood, paper, oil, clothing, etc.). Contact with metals may evolve flammable hydrogen gas. Containers may explode when heated.

Flammability and Explosibility

Ammonia vapor is slightly flammable (NFPA rating = 1) and ignites only with difficulty. Ammonia forms explosive mixtures with air in the range 16 to 25%. Water, carbon dioxide, or dry chemical extinguishers should be used for ammonia fires.

Agricultural Uses

Ammonium hydroxide is also known as ammonia solution, aqua ammonia, aqueous ammonia or ammonia liquor. It is the solution of ammonia in water and is commonly referred to as ammonium hydroxide. It is the simplest nitrogen solution made by forcing compressed ammonia (anhydrous ammonia) gas into water.

Safety Profile

A human poison by ingestion. An experimental poison by inhalation and ingestion. A severe eye irritant. Human systemic irritant effects by ocular and inhalation routes. Mutation data reported. Incompatible with acrolein, nitromethane, acrylic acid, chlorosulfonic acid, dimethyl sulfate, halogens, (Au + aqua regia), HCl, HF, HNO3, oleum, ppropiolactone, propylene oxide, AgNO3, Ag2O, (Ag20 + C2H5OH), AgMn04, H2SO4. Dangerous; liquid can inflict burns. Use with adequate ventilation. When heated to decomposition it emits NH3 and NO2.

Potential Exposure

It is used in detergents, stain removers, bleaches, dyes, fibers, and resins.

storage

All work with this substance should be conducted in a fume hood to prevent exposure by inhalation, and splash goggles and impermeable gloves should be worn at all times to prevent eye and skin contact. Containers should be tightly sealed to prevent escape of vapor and should be stored in a cool area separate from halogens, acids, and oxidizers. Containers stored in warm locations may build up dangerous internal pressures of ammonia gas.

Shipping

UN2672 Ammonia solutions, relative density between 0.880 and 0.957 at 15 C in water, with .10% but not .35% ammonia, Hazard class: 8; Labels: 8-Corrosive material.

Incompatibilities

Solution is strongly alkaline. Violent reaction with strong oxidizers, acids (exothermic reaction with strong mineral acids). Shock-sensitive compounds may be formed with halogens, mercury oxide; silver oxide. Fire and explosions may be caused by contact with β-propiolactone, silver nitrate; ethyl alcoho; silver permanganate; trimethylammonium amide; 1-chloro-2,4-dinitrobenzene, o-chloronitrobenzene, platinum, trioxygen difluoride; selenium difluoride dioxide; boron halides; mercury, chlorine, iodine; bromine, hypochlorites, chlorine bleach; amides, organic anhydrides; isocyanates, vinyl acetate; alkylene oxides; epichlorohydrin; aldehydes. Attacks some coatings, plastics and rubber. Attacks copper, brass, bronze, aluminum, steel, zinc, and their alloys.

Waste Disposal

Dilute with water, neutralize with HCl and discharge to sewer.

Check Digit Verification of cas no

The CAS Registry Mumber 1336-21-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,3,3 and 6 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1336-21:
(6*1)+(5*3)+(4*3)+(3*6)+(2*2)+(1*1)=56
56 % 10 = 6
So 1336-21-6 is a valid CAS Registry Number.
InChI:InChI=1/H3N.H2O/h1H3;1H2

1336-21-6 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • TCI America

  • (A2038)  Ammonia Solution (28% in Water)  

  • 1336-21-6

  • 500mL

  • 140.00CNY

  • Detail
  • Alfa Aesar

  • (33285)  Ammonium hydroxide, ACS, 28.0-30.0% NH3   

  • 1336-21-6

  • 250g

  • 217.0CNY

  • Detail
  • Alfa Aesar

  • (33285)  Ammonium hydroxide, ACS, 28.0-30.0% NH3   

  • 1336-21-6

  • 1kg

  • 409.0CNY

  • Detail
  • Alfa Aesar

  • (33285)  Ammonium hydroxide, ACS, 28.0-30.0% NH3   

  • 1336-21-6

  • *5x1kg

  • 1057.0CNY

  • Detail
  • Alfa Aesar

  • (38741)  Ammonium hydroxide, Environmental Grade, 20-22% NH3   

  • 1336-21-6

  • 500ml

  • 1023.0CNY

  • Detail
  • Alfa Aesar

  • (38742)  Ammonium hydroxide, Environmental Grade Plus, 20-22% NH3   

  • 1336-21-6

  • 250ml

  • 2020.0CNY

  • Detail
  • Alfa Aesar

  • (38742)  Ammonium hydroxide, Environmental Grade Plus, 20-22% NH3   

  • 1336-21-6

  • 500ml

  • 4723.0CNY

  • Detail
  • Alfa Aesar

  • (38742)  Ammonium hydroxide, Environmental Grade Plus, 20-22% NH3   

  • 1336-21-6

  • 1000ml

  • 8096.0CNY

  • Detail
  • Alfa Aesar

  • (88576)  Ammonium hydroxide, Acculute Standard Volumetric Solution, Final Concentration 0.1N   

  • 1336-21-6

  • 1unit

  • 223.0CNY

  • Detail
  • Alfa Aesar

  • (88576)  Ammonium hydroxide, Acculute Standard Volumetric Solution, Final Concentration 0.1N   

  • 1336-21-6

  • 6units

  • 1851.0CNY

  • Detail
  • Alfa Aesar

  • (35576)  Ammonium hydroxide, 0.1N Standardized Solution   

  • 1336-21-6

  • 1L

  • 286.0CNY

  • Detail
  • Alfa Aesar

  • (35576)  Ammonium hydroxide, 0.1N Standardized Solution   

  • 1336-21-6

  • 4L

  • 737.0CNY

  • Detail

1336-21-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name Ammonium hydroxide

1.2 Other means of identification

Product number -
Other names aqueous ammonia

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:1336-21-6 SDS

1336-21-6Synthetic route

sodium nitrate
7631-99-4

sodium nitrate

ammonium hydroxide
1336-21-6

ammonium hydroxide

Conditions
ConditionsYield
With phosphoric acid; hydrogen; nitric acid; palladium on activated charcoal; germanium dioxide at 40℃; Product distribution / selectivity;
ammonia borane complex
10043-11-5

ammonia borane complex

water
7732-18-5

water

ammonium hydroxide
1336-21-6

ammonium hydroxide

Conditions
ConditionsYield
Irradiation;
ammonia
7664-41-7

ammonia

silver nitrate

silver nitrate

sodium hydroxide
1310-73-2

sodium hydroxide

A

ammonium hydroxide
1336-21-6

ammonium hydroxide

B

diamminesilver(I) hydroxide
15291-89-1, 72021-02-4

diamminesilver(I) hydroxide

Conditions
ConditionsYield
In water
nitrogen
7727-37-9

nitrogen

water
7732-18-5

water

ammonium hydroxide
1336-21-6

ammonium hydroxide

Conditions
ConditionsYield
With air; Zn0.12Mo0.12Cd0.9S1.14/graphitic carbon nitride (g-C3N4)(20 mass percent) In ethanol at 30℃; under 760.051 Torr; Reagent/catalyst; Irradiation;
With hydrogenated Bi5O7I (H-Bi5O7I) at 15℃; Catalytic behavior; Reagent/catalyst; UV-irradiation;
With Bi5O7Br In neat (no solvent) Catalytic behavior; Mechanism; Reagent/catalyst; UV-irradiation;
With potassium sulfate Catalytic behavior; Reagent/catalyst; Electrochemical reaction;
With methanol Catalytic behavior; Irradiation;
nitrogen
7727-37-9

nitrogen

ammonium hydroxide
1336-21-6

ammonium hydroxide

Conditions
ConditionsYield
With sulfuric acid In water at 20℃; for 20h; Kinetics; Catalytic behavior; Electrochemical reaction;
sodium nitrate
7631-99-4

sodium nitrate

potassium hydroxide

potassium hydroxide

ammonium hydroxide
1336-21-6

ammonium hydroxide

Conditions
ConditionsYield
With ruthenium oxychloride In water at 25℃; Kinetics; Inert atmosphere; Electrolysis;
rubidium nitrate
13126-12-0

rubidium nitrate

potassium hydroxide

potassium hydroxide

ammonium hydroxide
1336-21-6

ammonium hydroxide

Conditions
ConditionsYield
With ruthenium oxychloride In water at 25℃; Kinetics; Inert atmosphere; Electrolysis;
caesium nitrate

caesium nitrate

potassium hydroxide

potassium hydroxide

ammonium hydroxide
1336-21-6

ammonium hydroxide

Conditions
ConditionsYield
With ruthenium oxychloride In water at 25℃; Kinetics; Inert atmosphere; Electrolysis;
potassium nitrate

potassium nitrate

potassium hydroxide

potassium hydroxide

ammonium hydroxide
1336-21-6

ammonium hydroxide

Conditions
ConditionsYield
With ruthenium oxychloride In water at 25℃; Kinetics; Mechanism; Reagent/catalyst; Concentration; Electrolysis; Inert atmosphere;
lithium nitrate

lithium nitrate

potassium hydroxide

potassium hydroxide

ammonium hydroxide
1336-21-6

ammonium hydroxide

Conditions
ConditionsYield
With ruthenium oxychloride In water at 25℃; Kinetics; Inert atmosphere; Electrolysis;
water
7732-18-5

water

oxygen
80937-33-3

oxygen

4-methyl-1,2-diaminobenzene
496-72-0

4-methyl-1,2-diaminobenzene

A

ammonium hydroxide
1336-21-6

ammonium hydroxide

B

carbon dioxide
124-38-9

carbon dioxide

Conditions
ConditionsYield
With Sr0.3Pb0.7TiO3/CoFe2O4 core-shell magnetic nanocomposite In aq. phosphate buffer at 20℃; for 0.00694444h; pH=7.1; Catalytic behavior; Concentration; pH-value; Electrochemical reaction; Green chemistry; chemoselective reaction;
nitrogen
7727-37-9

nitrogen

water
7732-18-5

water

A

ammonium hydroxide
1336-21-6

ammonium hydroxide

B

hydrogen
1333-74-0

hydrogen

Conditions
ConditionsYield
With potassium sulfate; FeReS3 for 192h; Mechanism; Kinetics; Time; Electrolysis;
ammonium hydroxide
1336-21-6

ammonium hydroxide

benzoyl chloride
98-88-4

benzoyl chloride

arabinosyl adenine
5536-17-4

arabinosyl adenine

N6-benzoyl-9-β-D-arabinofuranosyladenine
79896-97-2

N6-benzoyl-9-β-D-arabinofuranosyladenine

Conditions
ConditionsYield
With chloro-trimethyl-silane In pyridine; N-methyl-acetamide; methanol; water100%
With chloro-trimethyl-silane In pyridine; N-methyl-acetamide; methanol; water100%
With chloro-trimethyl-silane In pyridine; N-methyl-acetamide; methanol; water100%
ammonium hydroxide
1336-21-6

ammonium hydroxide

chloro-trimethyl-silane
75-77-4

chloro-trimethyl-silane

benzoyl chloride
98-88-4

benzoyl chloride

arabinosyl adenine
5536-17-4

arabinosyl adenine

N6-benzoyl-9-β-D-arabinofuranosyladenine
79896-97-2

N6-benzoyl-9-β-D-arabinofuranosyladenine

Conditions
ConditionsYield
In pyridine; N-methyl-acetamide; methanol; water100%
In pyridine; N-methyl-acetamide; methanol; water100%
In pyridine; N-methyl-acetamide; methanol; water100%
ammonium hydroxide
1336-21-6

ammonium hydroxide

cis-[4-cyano-4-(3-cyclopropylmethoxy-4-methoxyphenyl)-1-methoxycyclohexane-1-carboxylic acid]

cis-[4-cyano-4-(3-cyclopropylmethoxy-4-methoxyphenyl)-1-methoxycyclohexane-1-carboxylic acid]

isobutyl chloroformate
543-27-1

isobutyl chloroformate

Cis-[4-Cyano-4-(3-Cyclopropylmethoxy-4-Methoxyphenyl)-1-Methoxycyclohexane-1-Carboxamide]

Cis-[4-Cyano-4-(3-Cyclopropylmethoxy-4-Methoxyphenyl)-1-Methoxycyclohexane-1-Carboxamide]

Conditions
ConditionsYield
With 4-methyl-morpholine In 1,2-dimethoxyethane; water100%
ammonium hydroxide
1336-21-6

ammonium hydroxide

ethyl (4-methoxyphenyl)carbamodithioate
56134-95-3

ethyl (4-methoxyphenyl)carbamodithioate

1-(4-methoxyphenyl)thiourea
2293-07-4

1-(4-methoxyphenyl)thiourea

Conditions
ConditionsYield
at 60℃; Neat (no solvent);100%
ammonium hydroxide
1336-21-6

ammonium hydroxide

ammonium hexafluoridotechnetate(IV)

ammonium hexafluoridotechnetate(IV)

sodium fluoride

sodium fluoride

F10OTc2(4-)*5H3N*3H(1+)*Na(1+)*2FH

F10OTc2(4-)*5H3N*3H(1+)*Na(1+)*2FH

Conditions
ConditionsYield
In water at 20℃;100%
ammonium hydroxide
1336-21-6

ammonium hydroxide

C23H33ClN3ORe

C23H33ClN3ORe

C23H34N3O2Re

C23H34N3O2Re

Conditions
ConditionsYield
In dichloromethane at 20℃; for 2h; Inert atmosphere;100%
ammonium hydroxide
1336-21-6

ammonium hydroxide

PdCl(N,N-dimethylformamide)(μ-azobenzene)PdCl(N,N-dimethylformamide)
864439-66-7, 864439-72-5, 864515-21-9

PdCl(N,N-dimethylformamide)(μ-azobenzene)PdCl(N,N-dimethylformamide)

C12H14Cl2N4Pd2

C12H14Cl2N4Pd2

Conditions
ConditionsYield
In neat (no solvent) at 20℃; for 0.0833333h; Kinetics;100%
ammonium hydroxide
1336-21-6

ammonium hydroxide

magnus green salt

magnus green salt

tetrammineplatinum(II) chloride

tetrammineplatinum(II) chloride

Conditions
ConditionsYield
In water Heating;100%
ammonium hydroxide
1336-21-6

ammonium hydroxide

[platinum(II)(chloride)(η1-C2H4OMe)(1,10-phenanthroline)]
884655-84-9

[platinum(II)(chloride)(η1-C2H4OMe)(1,10-phenanthroline)]

[platinum(II)(ammonia)(η1-C2H4OMe)(1,10-phenanthroline)]chloride

[platinum(II)(ammonia)(η1-C2H4OMe)(1,10-phenanthroline)]chloride

Conditions
ConditionsYield
In water at 20℃; for 4.8h;99.9%
ammonium hydroxide
1336-21-6

ammonium hydroxide

Trichlorbutylstannan
1118-46-3

Trichlorbutylstannan

sodium carbonate
497-19-8

sodium carbonate

n-butylstannoic acid
2273-43-0

n-butylstannoic acid

Conditions
ConditionsYield
In water at 60℃; for 2.5h; Temperature;99.4%
ammonium hydroxide
1336-21-6

ammonium hydroxide

cycloserine
68-41-7

cycloserine

D-2-Amino-3-(aminooxy)propionic acid dihydrochloride

D-2-Amino-3-(aminooxy)propionic acid dihydrochloride

Conditions
ConditionsYield
In hydrogenchloride99%
ammonium hydroxide
1336-21-6

ammonium hydroxide

4-butylbenzoyl chloride
28788-62-7

4-butylbenzoyl chloride

4-n-butylbenzamide
107377-07-1

4-n-butylbenzamide

Conditions
ConditionsYield
99%
ammonium hydroxide
1336-21-6

ammonium hydroxide

C4H19B12O2(1-)*2C16H36N(1+)

C4H19B12O2(1-)*2C16H36N(1+)

tetra(n-butyl)ammonium hydroxide
2052-49-5

tetra(n-butyl)ammonium hydroxide

2- (2-aminoethoxy)ethoxyundecahydrocrossodedecaborate ditetrabutylammonium salt

2- (2-aminoethoxy)ethoxyundecahydrocrossodedecaborate ditetrabutylammonium salt

Conditions
ConditionsYield
Stage #1: ammonium hydroxide; C4H19B12O2(1-)*2C16H36N(1+) In acetonitrile at 50℃; for 11h;
Stage #2: tetra(n-butyl)ammonium hydroxide In methanol
99%
ammonium hydroxide
1336-21-6

ammonium hydroxide

dihydrogen peroxide
7722-84-1

dihydrogen peroxide

germanium dioxide

germanium dioxide

Ge6H6O24(6-)*6H4N(1+)*6H2O

Ge6H6O24(6-)*6H4N(1+)*6H2O

Conditions
ConditionsYield
pH=9;98.3%
ammonium hydroxide
1336-21-6

ammonium hydroxide

C14H13BrF4N2O
1352420-03-1

C14H13BrF4N2O

C14H15F4N3O
1352420-05-3

C14H15F4N3O

Conditions
ConditionsYield
Stage #1: C14H13BrF4N2O With copper(l) iodide; sodium carbonate; N,N`-dimethylethylenediamine In dimethyl sulfoxide at 110℃; for 6h;
Stage #2: ammonium hydroxide In water
98%
ammonium hydroxide
1336-21-6

ammonium hydroxide

methane
34557-54-5

methane

[4-(4-{2-[Bis-((2R,3S)-2,3,4-trihydroxybutyl)amino]ethoxy}phenyl)butyl]carbamic acid tert-butyl ester

[4-(4-{2-[Bis-((2R,3S)-2,3,4-trihydroxybutyl)amino]ethoxy}phenyl)butyl]carbamic acid tert-butyl ester

4-[N,N-bis-((2S,3R)-2,3,4-trihydroxybutyl)-2-aminoethoxy]phenylbutylamine

4-[N,N-bis-((2S,3R)-2,3,4-trihydroxybutyl)-2-aminoethoxy]phenylbutylamine

Conditions
ConditionsYield
In ethanol; dichloromethane98%
ammonium hydroxide
1336-21-6

ammonium hydroxide

2C16H36N(1+)*6NO3(1-)*Mo6Br8(4+)

2C16H36N(1+)*6NO3(1-)*Mo6Br8(4+)

A

14H2O*4HO(1-)*Mo6Br8(4+)

14H2O*4HO(1-)*Mo6Br8(4+)

B

4H2O*4HO(1-)*Mo6Br8(4+)

4H2O*4HO(1-)*Mo6Br8(4+)

Conditions
ConditionsYield
In acetone for 12h;A n/a
B 97.6%
ammonium hydroxide
1336-21-6

ammonium hydroxide

dihydrogen peroxide
7722-84-1

dihydrogen peroxide

germaniumtetrachloride
10038-98-9

germaniumtetrachloride

Ge6H6O24(6-)*6H4N(1+)*6H2O

Ge6H6O24(6-)*6H4N(1+)*6H2O

Conditions
ConditionsYield
pH=9;97.2%
ammonium hydroxide
1336-21-6

ammonium hydroxide

glycine
56-40-6

glycine

copper(II) oxide

copper(II) oxide

copper(II) glycinate monohydrate

copper(II) glycinate monohydrate

Conditions
ConditionsYield
Stage #1: ammonium hydroxide; copper(II) oxide at 20℃; for 0.833333h;
Stage #2: glycine at 95℃; for 2h; Concentration; Temperature;
96.8%
ammonium hydroxide
1336-21-6

ammonium hydroxide

potassium 3-(((3',5'-di-O-acetyl)-β-D-2-deoxyribofuranosyl)-6-((2-(2-(H)-1,10,2,20-tetracarba-3-commo-cobalta-closo-tricosaborate-8-yl)oxyethoxy)ethoxy)methyl)furo[2,3-d]pyrimidin-2(3H)-one

potassium 3-(((3',5'-di-O-acetyl)-β-D-2-deoxyribofuranosyl)-6-((2-(2-(H)-1,10,2,20-tetracarba-3-commo-cobalta-closo-tricosaborate-8-yl)oxyethoxy)ethoxy)methyl)furo[2,3-d]pyrimidin-2(3H)-one

potassium 3-(β-D-2-deoxyribofuranosyl)-3,7-dihydro-6-(((2-(2-(H)-1,10,2,20-tetracarba-3-commo-cobalta-closo-tricosaborate-8-yl)oxyethoxy)ethoxy)methyl)pyrrolo[2,3-d]pyrimidin-2(3H)-one

potassium 3-(β-D-2-deoxyribofuranosyl)-3,7-dihydro-6-(((2-(2-(H)-1,10,2,20-tetracarba-3-commo-cobalta-closo-tricosaborate-8-yl)oxyethoxy)ethoxy)methyl)pyrrolo[2,3-d]pyrimidin-2(3H)-one

Conditions
ConditionsYield
With potassium carbonate In water96%
ammonium hydroxide
1336-21-6

ammonium hydroxide

potassium 3-(((3',5'-di-O-acetyl)-β-D-2-deoxyribofuranosyl)-6-((5-((H)-1,10,2,20-tetracarba-3-commo-cobalta-closo-tricosaborate)-8-yl)oxypentyloxy)ethyl)furo[2,3-d]pyrimidin-2(3H)-one

potassium 3-(((3',5'-di-O-acetyl)-β-D-2-deoxyribofuranosyl)-6-((5-((H)-1,10,2,20-tetracarba-3-commo-cobalta-closo-tricosaborate)-8-yl)oxypentyloxy)ethyl)furo[2,3-d]pyrimidin-2(3H)-one

potassium 3-(β-D-2-deoxyribofuranosyl)-3,7-dihydro-6-(((5-((H)-1,10,2,20-tetracarba-3-commo-cobalta-closo-tricosaborate)-8-yl)oxypentyloxy)ethyl)pyrrolo[2,3-d]pyrimidin-2(3H)-one

potassium 3-(β-D-2-deoxyribofuranosyl)-3,7-dihydro-6-(((5-((H)-1,10,2,20-tetracarba-3-commo-cobalta-closo-tricosaborate)-8-yl)oxypentyloxy)ethyl)pyrrolo[2,3-d]pyrimidin-2(3H)-one

Conditions
ConditionsYield
With potassium carbonate In water96%
ammonium hydroxide
1336-21-6

ammonium hydroxide

p-nitroacetanilide-15N
61629-37-6

p-nitroacetanilide-15N

<15N>p-nitroaniline
24176-48-5

<15N>p-nitroaniline

Conditions
ConditionsYield
Stage #1: p-nitroacetanilide-15N With hydrogenchloride In water for 24h; Reflux;
Stage #2: ammonium hydroxide In water at 0℃;
96%
ammonium hydroxide
1336-21-6

ammonium hydroxide

benzoyl chloride
98-88-4

benzoyl chloride

2'-Deoxycytidine
951-77-9

2'-Deoxycytidine

N4-benzoyl-2'-deoxycytidine
4836-13-9

N4-benzoyl-2'-deoxycytidine

Conditions
ConditionsYield
Stage #1: 2'-Deoxycytidine With pyridine; chloro-trimethyl-silane
Stage #2: benzoyl chloride With pyridine
Stage #3: ammonium hydroxide
96%
ammonium hydroxide
1336-21-6

ammonium hydroxide

zirconium(IV) chloride
10026-11-6

zirconium(IV) chloride

zirconium hydroxide

zirconium hydroxide

Conditions
ConditionsYield
In water at 20℃; for 24h; pH=11;96%
ammonium hydroxide
1336-21-6

ammonium hydroxide

2-bromonaphthalene
580-13-2

2-bromonaphthalene

trimethyltin(IV)chloride
1066-45-1

trimethyltin(IV)chloride

tert.-butyl lithium
594-19-4

tert.-butyl lithium

A

1-(trimethylstannyl)naphthalene
944-85-4

1-(trimethylstannyl)naphthalene

B

β-naphthyltrimethylstannane
945-77-7

β-naphthyltrimethylstannane

Conditions
ConditionsYield
In 1,4-dioxane; diethyl ether; pentaneA 95.6%
B n/a
ammonium hydroxide
1336-21-6

ammonium hydroxide

2C16H36N(1+)*6NO3(1-)*Mo6Cl8(4+)

2C16H36N(1+)*6NO3(1-)*Mo6Cl8(4+)

A

14H2O*4HO(1-)*Mo6Cl8(4+)

14H2O*4HO(1-)*Mo6Cl8(4+)

B

4H2O*4HO(1-)*Mo6Cl8(4+)

4H2O*4HO(1-)*Mo6Cl8(4+)

Conditions
ConditionsYield
In acetone for 12h;A n/a
B 95.5%
ammonium hydroxide
1336-21-6

ammonium hydroxide

water
7732-18-5

water

acetic acid
64-19-7

acetic acid

palladium dichloride

palladium dichloride

C8H20N4O8Pd4*11H2O

C8H20N4O8Pd4*11H2O

Conditions
ConditionsYield
Stage #1: ammonium hydroxide; palladium dichloride at 50℃; Inert atmosphere;
Stage #2: water With barium(II) hydroxide for 24h; Cooling with ice;
Stage #3: acetic acid With acetamide at 20℃; for 48h; Inert atmosphere;
95.46%
ammonium hydroxide
1336-21-6

ammonium hydroxide

potassium tetrachloroplatinate(II)
10025-99-7

potassium tetrachloroplatinate(II)

potassium iodide
7681-11-0

potassium iodide

cis-diamminediiodoplatinum (II)
13841-96-8, 15978-93-5, 15978-94-6

cis-diamminediiodoplatinum (II)

Conditions
ConditionsYield
Stage #1: potassium tetrachloroplatinate(II); potassium iodide In water at 40 - 60℃; Darkness;
Stage #2: ammonium hydroxide In water Darkness;
95.1%
Stage #1: potassium tetrachloroplatinate(II); potassium iodide In water at 50℃; for 0.0833333h;
Stage #2: ammonium hydroxide In water for 3h;
89%
In water at 50 - 60℃; Inert atmosphere;80%
(3S,4S)-4-[(S)-3-(4-fluorobenzyl)-piperidin-1-ylmethyl]-1,1-dioxo-tetrahydro-thiophen-3-ylamine
388109-44-2

(3S,4S)-4-[(S)-3-(4-fluorobenzyl)-piperidin-1-ylmethyl]-1,1-dioxo-tetrahydro-thiophen-3-ylamine

ammonium hydroxide
1336-21-6

ammonium hydroxide

3-acetylphenyl isocyanate
23138-64-9

3-acetylphenyl isocyanate

1-{(3S,4S)-4-[(S)-3-(4-fluorobenzyl)-piperidin-1-ylmethyl]-1,1-dioxo-tetrahydrothiophen-3-yl}-3-[3-acetylphenyl]-urea, trifluoroacetate salt

1-{(3S,4S)-4-[(S)-3-(4-fluorobenzyl)-piperidin-1-ylmethyl]-1,1-dioxo-tetrahydrothiophen-3-yl}-3-[3-acetylphenyl]-urea, trifluoroacetate salt

Conditions
ConditionsYield
With triethylamine; trifluoroacetic acid In methanol; water; N,N-dimethyl-formamide; acetonitrile95%
ammonium hydroxide
1336-21-6

ammonium hydroxide

2,4-difluorobenzene-1-sulfonyl chloride
13918-92-8

2,4-difluorobenzene-1-sulfonyl chloride

2,4-difluoro-1-benzenesulfonamide
13656-60-5

2,4-difluoro-1-benzenesulfonamide

Conditions
ConditionsYield
In dichloromethane; ethyl acetate95%

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1336-21-6Relevant articles and documents

Electrospun Cu-doped titania nanofibers for photocatalytic hydrolysis of ammonia borane

Yousef, Ayman,Barakat, Nasser A.M.,Kim, Hak Yong

, p. 98 - 106 (2013)

Among reported hydrogen storage materials, ammonia borane is a promising candidate to be utilized in many industrial applications. The high chemical resistance of the ceramic catalysts makes them one of the most stable classes of catalytic materials. In this study, CuO nanoparticles (NPs) -doped TiO 2 nanofibers (NFs) are introduced as a highly effective and reusable catalyst for ammonia borane complex hydrolysis. The incorporation of CuO NPs inside the TiO2 NFs provided distinct advantages for the introduced catalyst; the aggregation problem of the CuO NPs was overcome and a synergistic effect was created as the synthesized CuO NPs-doped TiO2 revealed higher activity compared to the individual components. Typically, after 10 min, the obtained hydrogen equivalent was 2.7, 0.9 and 0.95 when CuO NPs-doped TiO2 nanofibers, CuO NPs and pristine TiO2 nanofibers were used as the catalyst, respectively. The catalytic activity of the introduced nanofibers did not change after being used for three successive cycles. Moreover, the catalytic performance was strongly modified when the hydrolysis process was performed under sunlight irradiation because of the photocatalytic activity of the TiO2 and CuO. The introduced nanofibers were prepared by the simple, effective, low cost and high yielding technique of electrospinning. The present study introduces TiO2 nanofibers as a promising catalyst for the ammonia borane complex, as well as an interesting support used for functional materials.

S-Doped three-dimensional graphene (S-3DG): A metal-free electrocatalyst for the electrochemical synthesis of ammonia under ambient conditions

Wang, Jin,Wang, Shuang,Li, Jinping

, p. 2258 - 2263 (2020)

In this study, we report sulfur-doped three-dimensional graphene (S-3DG) as a metal-free electrocatalyst for N2 reduction reaction (NRR) under ambient conditions. Due to the high electron transport capacity and stable physicochemical properties

Effect of carbon and nitrogen double vacancies on the improved photocatalytic hydrogen evolution over porous carbon nitride nanosheets

Li, Huihui,Ning, Fuchun,Chen, Xiaofei,Shi, Anye

, p. 3270 - 3278 (2021)

Porous carbon nitride nanosheets with carbon and nitrogen double vacancies have been synthesized by a soft template-supported one-pot method. Besides their highly defined and unambiguous structure, they also show minimal thickness and high crystallinity.

In-situ formation of bismuth nanoparticles on nickel foam for ambient ammonia synthesis via electrocatalytic nitrogen reduction

Li, Guangzhe,Pan, Zhefei,Lin, He,An, Liang

, (2021/05/04)

Bismuth has been regarded as a promising electrocatalyst for triggering nitrogen reduction to ammonia, due to the ease of nitrogen dissociation rendered by the strong interaction between Bi 6p band and the N 2p orbitals. However, the poor conductivity of bismuth limits the electron transfer for nitrogen reduction. In addition, the sluggish water dissociation on the bismuth surface leads to insufficient proton supply for the protonation step of *N2, causing inferior ammonia production performance. In this work, we prepare an integrated and binder-free bismuth nanoparticles@nickel foam electrode for ambient ammonia synthesis via a facile displacement reaction. Using nickel foam as the conductive substrate improves the electron transfer of bismuth for nitrogen reduction to ammonia. In addition, enhanced water dissociation on the nickel surface improves the protonation of *N2 by supplying adequate protons via hydrogen spillover, thus boosting the ammonia production performance. This integrated electrode eliminates the use of polymer binders and reduces the contact resistance between the diffusion layer and catalyst layer, facilitating electron delivery and reducing cell resistance, thus requiring less energy input for ammonia production. The performance examination in an electrochemical H-type cell shows that an ammonia yield rate as high as of 9.3 × 10?11 mol s?1 cm?2 and a Faradaic efficiency of 6.3% are achieved. An ammonia yield rate of 8.19 × 10?11 mol s?1 cm?2 is observed after 6 cycles, with a retention rate of 88%.

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