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75-59-2 Usage

Description

Tetramethylammonium hydroxide is a solid in the hydrated form or a colorless liquid with a strong ammonia-like odor. It is soluble in water, and corrosive to metals and tissue.

Uses

Different sources of media describe the Uses of 75-59-2 differently. You can refer to the following data:
1. ▼▲ Industry Application Role/benefit Organic silicon Production of dimethyl silicone oil, organic silicon resin, silicon rubber, etc. Catalyst/removed easily; no pollution to the products Chemical analysis Polarography experiment Polarographic reagent Thermochemolysis to study fungal degradation of wood Analytical reagent Chemical purification Removal of metal elements Ash free alkali/source of base; make the metal elements precipitated Electron Production of computer silicon chip Brightening agent; anisotropic etching agent; cleaning agent; photoresist developer Printing of circuit board Cleaning agent Semiconductor manufacturing Chemical stripper Others Synthesis of ferrofluid Surfactant/ inhibit nanoparticle aggregation Synthesis of zeolite Structure directing agent
2. Tetramethylammonium hydroxide is used to produce tetramethyl-ammonium azide. It is used as an anisotropic etchant of silicon, basic solvent in the development of acidic photoresist in photolithography process, as surfactant in the synthesis of ferrofluid and as a polarographic reagent. It finds application in the production of organic silicon, where it is used for computer silicon wafer surface brightener and cleaning agent. It is also involved in the purification of some metallic elements.
3. Tetramethylammonium hydroxide solution (25 wt.% solution in water) may be used as a base for pH adjustment to obtain hexagonal mesoporous aluminophosphate (TAP).

General Description

Tetramethylammonium hydroxide is a quaternary ammonium salt generally used as an anisotropic etchant for silicon due to its high silicon etching rate.

Reactivity Profile

Tetramethylammonium hydroxide acts like a base. Bases are chemically similar to sodium hydroxide (NaOH) or sodium oxide (Na2O). They neutralize acids exothermically to form salts plus water. When soluble in water they give solutions having a pH greater than 7.0. Mixing these materials with water can generate troublesome amounts of heat as the base is dissolved or diluted. Bases react with certain metals (such as aluminum and zinc) to form oxides or hydroxides of the metal and generate gaseous hydrogen. Bases may initiate polymerization reactions in polymerizable organic compounds, especially epoxides). They may generate flammable and/or toxic gases with ammonium salts, nitrides, halogenated organics, various metals, peroxides, and hydroperoxides. Materials of this group often serve as catalysts.

Health Hazard

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

Combustible material: may burn but does not ignite readily. When heated, vapors may form explosive mixtures with air: indoors, outdoors and sewers explosion hazards. Contact with metals may evolve flammable hydrogen gas. Containers may explode when heated. Runoff may pollute waterways. Substance may be transported in a molten form.

Safety Profile

Poison by subcutaneous route. A powerful caustic. A corrosive irritant to skin, eyes, and mucous membranes. When heated to decomposition it emits toxic fumes of NOx and NH3.

References

1.https://en.wikipedia.org/wiki/Tetramethylammonium_hydroxide#Uses 2.http://sacheminc.com/other-chemicals/tetramethylammonium-hydroxide-tmah/ 3.https://www.fs.usda.gov/treesearch/pubs/15506 4.https://www.concordia.ca/content/dam/concordia/services/safety/docs/EHS-DOC-020_TMAHGuidelines.pdf 5.http://www.lookchem.com/ChemicalProductProperty_EN_CB2854236.htm

Check Digit Verification of cas no

The CAS Registry Mumber 75-59-2 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 7 and 5 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 75-59:
(4*7)+(3*5)+(2*5)+(1*9)=62
62 % 10 = 2
So 75-59-2 is a valid CAS Registry Number.
InChI:InChI=1/C4H12N.H2O/c1-5(2,3)4;/h1-4H3;1H2/q+1;/p-1

75-59-2 Well-known Company Product Price

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  • (Code)Product description
  • CAS number
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  • Detail
  • TCI America

  • (T0676)  Tetramethylammonium Hydroxide (10% in Methanol)  

  • 75-59-2

  • 25mL

  • 135.00CNY

  • Detail
  • TCI America

  • (T0676)  Tetramethylammonium Hydroxide (10% in Methanol)  

  • 75-59-2

  • 100mL

  • 345.00CNY

  • Detail
  • TCI America

  • (T0676)  Tetramethylammonium Hydroxide (10% in Methanol)  

  • 75-59-2

  • 500mL

  • 735.00CNY

  • Detail
  • Alfa Aesar

  • (L09991)  Tetramethylammonium hydroxide, 25% w/w aq. soln.   

  • 75-59-2

  • 25ml

  • 111.0CNY

  • Detail
  • Alfa Aesar

  • (L09991)  Tetramethylammonium hydroxide, 25% w/w aq. soln.   

  • 75-59-2

  • 100ml

  • 254.0CNY

  • Detail
  • Alfa Aesar

  • (L09991)  Tetramethylammonium hydroxide, 25% w/w aq. soln.   

  • 75-59-2

  • 250ml

  • 517.0CNY

  • Detail
  • Alfa Aesar

  • (L09991)  Tetramethylammonium hydroxide, 25% w/w aq. soln.   

  • 75-59-2

  • 500ml

  • 827.0CNY

  • Detail
  • Alfa Aesar

  • (L09991)  Tetramethylammonium hydroxide, 25% w/w aq. soln.   

  • 75-59-2

  • 1000ml

  • 1491.0CNY

  • Detail
  • Alfa Aesar

  • (L09991)  Tetramethylammonium hydroxide, 25% w/w aq. soln.   

  • 75-59-2

  • 2500ml

  • 3131.0CNY

  • Detail
  • Alfa Aesar

  • (20932)  Tetramethylammonium hydroxide, 25% w/w aq. soln., Electronic Grade, 99.9999% (metals basis)   

  • 75-59-2

  • 250ml

  • 390.0CNY

  • Detail
  • Alfa Aesar

  • (20932)  Tetramethylammonium hydroxide, 25% w/w aq. soln., Electronic Grade, 99.9999% (metals basis)   

  • 75-59-2

  • 1L

  • 1345.0CNY

  • Detail
  • Alfa Aesar

  • (20932)  Tetramethylammonium hydroxide, 25% w/w aq. soln., Electronic Grade, 99.9999% (metals basis)   

  • 75-59-2

  • 1gal

  • 2032.0CNY

  • Detail

75-59-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Tetramethylammonium hydroxide

1.2 Other means of identification

Product number -
Other names tetreamethyl ammonium hydroxide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
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:75-59-2 SDS

75-59-2Synthetic route

methanol
67-56-1

methanol

carbonic acid dimethyl ester
616-38-6

carbonic acid dimethyl ester

trimethylamine
75-50-3

trimethylamine

tetramethyl ammoniumhydroxide
75-59-2

tetramethyl ammoniumhydroxide

Conditions
ConditionsYield
Stage #1: methanol; carbonic acid dimethyl ester; trimethylamine In water at 140℃; under 11251.1 Torr; for 4h;
Stage #2: With calcium hydroxide In methanol; water Heating / reflux;
95.2%
tetramethylammonium bromide
64-20-0

tetramethylammonium bromide

tetramethyl ammoniumhydroxide
75-59-2

tetramethyl ammoniumhydroxide

Conditions
ConditionsYield
With potassium hydroxide In dichloromethane at 20℃; for 10h;68%
With water; silver(l) oxide die Salze entstehen; und Eindunsten des Filtrats Vakuum ueber Schwefelsaeure;
With potassium hydroxide In ethanol at 20℃; for 12h;
methanol
67-56-1

methanol

methyl nitrate
598-58-3

methyl nitrate

tetramethyl ammoniumhydroxide
75-59-2

tetramethyl ammoniumhydroxide

Conditions
ConditionsYield
With ammonia die Salze entstehen;
tertamethylammonium iodide
75-58-1

tertamethylammonium iodide

tetramethyl ammoniumhydroxide
75-59-2

tetramethyl ammoniumhydroxide

Conditions
ConditionsYield
With water Herstellung einer wss. Loesung mit Hilfe eines Anionenaustauschers;
tetramethlyammonium chloride
75-57-0

tetramethlyammonium chloride

tetramethyl ammoniumhydroxide
75-59-2

tetramethyl ammoniumhydroxide

Conditions
ConditionsYield
With methanol; potassium hydroxide man filtriert vom ausgescheidenen Kaliumchlorid ab und engt unter Zuatz von Wasser im Vakuum bei 35grad ein;
With potassium hydroxide In methanol at 25℃; for 2h;
With sodium hydroxide In ethanol for 4h;
methyl bromide
74-83-9

methyl bromide

dimethyl amine
124-40-3

dimethyl amine

tetramethyl ammoniumhydroxide
75-59-2

tetramethyl ammoniumhydroxide

Conditions
ConditionsYield
With methanol at 100℃; die Salze entstehen;
methyl nitrate
598-58-3

methyl nitrate

dimethyl amine
124-40-3

dimethyl amine

tetramethyl ammoniumhydroxide
75-59-2

tetramethyl ammoniumhydroxide

Conditions
ConditionsYield
With methanol at 100℃; die Salze entstehen;
dimethyl amine
124-40-3

dimethyl amine

methyl iodide
74-88-4

methyl iodide

tetramethyl ammoniumhydroxide
75-59-2

tetramethyl ammoniumhydroxide

Conditions
ConditionsYield
With methanol at 100℃; die Salze entstehen;
dimethyl sulfate
77-78-1

dimethyl sulfate

trimethylamine
75-50-3

trimethylamine

tetramethyl ammoniumhydroxide
75-59-2

tetramethyl ammoniumhydroxide

Conditions
ConditionsYield
Kochen des erhaltenen Methylsulfats mit verd.H2SO4 und anschliessende Umsetzung mit Ba(OH)2;
methyl bromide
74-83-9

methyl bromide

methylamine
74-89-5

methylamine

tetramethyl ammoniumhydroxide
75-59-2

tetramethyl ammoniumhydroxide

Conditions
ConditionsYield
With methanol at 100℃; die Salze entstehen;
methyl nitrate
598-58-3

methyl nitrate

methylamine
74-89-5

methylamine

tetramethyl ammoniumhydroxide
75-59-2

tetramethyl ammoniumhydroxide

Conditions
ConditionsYield
With methanol at 100℃; die Salze entstehen;
methylamine
74-89-5

methylamine

methyl iodide
74-88-4

methyl iodide

tetramethyl ammoniumhydroxide
75-59-2

tetramethyl ammoniumhydroxide

Conditions
ConditionsYield
With methanol at 100℃; die Salze entstehen;
acetylene
74-86-2

acetylene

trimethylamine
75-50-3

trimethylamine

tetramethyl ammoniumhydroxide
75-59-2

tetramethyl ammoniumhydroxide

Conditions
ConditionsYield
With water at 105℃; unter Druck;
methyl bromide
74-83-9

methyl bromide

trimethylamine
75-50-3

trimethylamine

tetramethyl ammoniumhydroxide
75-59-2

tetramethyl ammoniumhydroxide

Conditions
ConditionsYield
die Salze entstehen;
methylene chloride
74-87-3

methylene chloride

trimethylamine
75-50-3

trimethylamine

tetramethyl ammoniumhydroxide
75-59-2

tetramethyl ammoniumhydroxide

Conditions
ConditionsYield
die Salze entstehen;
trimethyl-vinylammonium cation
13448-18-5

trimethyl-vinylammonium cation

trimethylamine
75-50-3

trimethylamine

tetramethyl ammoniumhydroxide
75-59-2

tetramethyl ammoniumhydroxide

Conditions
ConditionsYield
With water at 110 - 120℃;
methyl iodide
74-88-4

methyl iodide

tetramethyl ammoniumhydroxide
75-59-2

tetramethyl ammoniumhydroxide

Conditions
ConditionsYield
With ammonia; water die Salze entstehen;
With ethanol; ammonia die Salze entstehen;
Tetramethylammonium hydrogen carbonate
58345-96-3

Tetramethylammonium hydrogen carbonate

tetramethyl ammoniumhydroxide
75-59-2

tetramethyl ammoniumhydroxide

Conditions
ConditionsYield
With water for 12h; electrolysis (20V);626 g
With hydrogenchloride; formic acid; sulfuric acid In water electrolysis;
tetramethyl-triphenylmethyl-ammonium

tetramethyl-triphenylmethyl-ammonium

tetramethyl ammoniumhydroxide
75-59-2

tetramethyl ammoniumhydroxide

Conditions
ConditionsYield
With water
trimethylacetonylammonium bromide

trimethylacetonylammonium bromide

tetramethyl ammoniumhydroxide
75-59-2

tetramethyl ammoniumhydroxide

Conditions
ConditionsYield
at 195 - 200℃; die Salze entstehen;
methyl iodide
74-88-4

methyl iodide

trimethylazonium iodide

trimethylazonium iodide

tetramethyl ammoniumhydroxide
75-59-2

tetramethyl ammoniumhydroxide

Conditions
ConditionsYield
With methanol at 125 - 130℃; die Salze entstehen;
methyl nitrate
598-58-3

methyl nitrate

A

tetramethyl ammoniumhydroxide
75-59-2

tetramethyl ammoniumhydroxide

B

water
7732-18-5

water

Conditions
ConditionsYield
With ammonia die Salze entstehen; bei laengerem Stehen;
With ammonia die Salze entstehen; beim Erhitzen;
methanol
67-56-1

methanol

A

tetramethyl ammoniumhydroxide
75-59-2

tetramethyl ammoniumhydroxide

B

hydrochloride of trimethylamine

hydrochloride of trimethylamine

Conditions
ConditionsYield
With ammonium chloride at 285℃; die Salze entstehen;
tetramethylammonium sulfate

tetramethylammonium sulfate

tetramethyl ammoniumhydroxide
75-59-2

tetramethyl ammoniumhydroxide

Conditions
ConditionsYield
With ambersep 900 OH In water Product distribution / selectivity; Alkaline conditions;
In sulfuric acid; water for 6h; Product distribution / selectivity; Electrolysis;
tris(tetramethylammonium) phosphate

tris(tetramethylammonium) phosphate

tetramethyl ammoniumhydroxide
75-59-2

tetramethyl ammoniumhydroxide

Conditions
ConditionsYield
With basic anion exchanger In water Product distribution / selectivity;
Cyclohexanethiol
1569-69-3

Cyclohexanethiol

tetramethyl ammoniumhydroxide
75-59-2

tetramethyl ammoniumhydroxide

Cyclohexanethiolatetetramethyl-ammonium;
138555-12-1

Cyclohexanethiolatetetramethyl-ammonium;

Conditions
ConditionsYield
In benzene at 6 - 10℃; for 1h;100%
bis-p-phenylene-34-crown-10-12,152-dicarboxylic acid
1030850-30-6

bis-p-phenylene-34-crown-10-12,152-dicarboxylic acid

tetramethyl ammoniumhydroxide
75-59-2

tetramethyl ammoniumhydroxide

bis(tetramethylammonium) bis-p-phenylene-34-crown-10-12,152-dicarboxylate

bis(tetramethylammonium) bis-p-phenylene-34-crown-10-12,152-dicarboxylate

Conditions
ConditionsYield
In methanol for 2h;100%
Homotaurin
3687-18-1

Homotaurin

tetramethyl ammoniumhydroxide
75-59-2

tetramethyl ammoniumhydroxide

acetic anhydride
108-24-7

acetic anhydride

tetramethylammonium N-acetylhomotaurinate
1131569-67-9

tetramethylammonium N-acetylhomotaurinate

Conditions
ConditionsYield
Stage #1: Homotaurin; tetramethyl ammoniumhydroxide In water at 20℃; for 1h;
Stage #2: acetic anhydride In water at 40℃;
100%
Stage #1: Homotaurin; tetramethyl ammoniumhydroxide In water at 20℃; for 1h;
Stage #2: acetic anhydride In water at 40℃;
100%
Stage #1: Homotaurin; tetramethyl ammoniumhydroxide In water at 20℃; for 1h;
Stage #2: acetic anhydride In water at 40℃;
100%
C29H28N2O7S
1160694-10-9

C29H28N2O7S

tetramethyl ammoniumhydroxide
75-59-2

tetramethyl ammoniumhydroxide

C4H12N(1+)*C29H27N2O7S(1-)

C4H12N(1+)*C29H27N2O7S(1-)

Conditions
ConditionsYield
In methanol; dichloromethane at -78℃;100%
tetramethyl ammoniumhydroxide
75-59-2

tetramethyl ammoniumhydroxide

benzoic acid
65-85-0

benzoic acid

tetramethylammonium benzoate
25255-90-7

tetramethylammonium benzoate

Conditions
ConditionsYield
With water In ethanol at 0 - 20℃; for 0.0833333h;100%
In methanol at 45℃; for 4h;75%
In methanol
tetramethyl ammoniumhydroxide
75-59-2

tetramethyl ammoniumhydroxide

diguanidine carbonate
593-85-1

diguanidine carbonate

cis,cis-1,3,5-trimethylcyclohexane-1,3,5-tricarboxylic acid

cis,cis-1,3,5-trimethylcyclohexane-1,3,5-tricarboxylic acid

[(CH3)4N(+)]*2[C(NH2)3(+)]*[KTA(3-)]

[(CH3)4N(+)]*2[C(NH2)3(+)]*[KTA(3-)]

Conditions
ConditionsYield
In water at 40℃;100%
tetraethoxy orthosilicate
78-10-4

tetraethoxy orthosilicate

tetramethyl ammoniumhydroxide
75-59-2

tetramethyl ammoniumhydroxide

octakis(tetramethylammonium)silsesquioxane

octakis(tetramethylammonium)silsesquioxane

Conditions
ConditionsYield
In methanol; water at 20℃; Cooling with ice; Inert atmosphere;100%
In methanol; water at 20℃; for 24h; Inert atmosphere;97%
In methanol; water at 20℃; for 24h; Cooling with ice;97%
C30H24O12
1305346-38-6

C30H24O12

tetramethyl ammoniumhydroxide
75-59-2

tetramethyl ammoniumhydroxide

ethylenediamine
107-15-3

ethylenediamine

6C4H12N(1+)*C66H54N6O18(6-)

6C4H12N(1+)*C66H54N6O18(6-)

Conditions
ConditionsYield
With [D]-sodium hydroxide; sodium acetate In water-d2 for 2h; pD >11;100%
1,2-benzisothiazolin-3-one
2634-33-5

1,2-benzisothiazolin-3-one

tetramethyl ammoniumhydroxide
75-59-2

tetramethyl ammoniumhydroxide

tetramethylammonium 1,2-benzisothiazol-3-one
400089-65-8

tetramethylammonium 1,2-benzisothiazol-3-one

Conditions
ConditionsYield
In water pH=9.58;100%
In water pH=9.0;
tetramethyl ammoniumhydroxide
75-59-2

tetramethyl ammoniumhydroxide

phenol
108-95-2

phenol

tetramethylammonium phenoxide
36439-44-8

tetramethylammonium phenoxide

Conditions
ConditionsYield
Stage #1: tetramethyl ammoniumhydroxide; phenol In water for 0.0166667h;
Stage #2: at 70℃; for 72h;
100%
In water at 25℃; for 0.166667h;96%
In ethanol; water at 20℃; for 24h; Inert atmosphere;
tetramethyl ammoniumhydroxide
75-59-2

tetramethyl ammoniumhydroxide

p-N,N-dimethylaminobenzoic acid
619-84-1

p-N,N-dimethylaminobenzoic acid

tetramethylammonium 4-(dimethylamino)benzoate
70697-58-4

tetramethylammonium 4-(dimethylamino)benzoate

Conditions
ConditionsYield
With water In ethanol at 0 - 20℃; for 0.0833333h;100%
In ethanol; water for 1h;
deuterated formic acid
917-71-5

deuterated formic acid

tetramethyl ammoniumhydroxide
75-59-2

tetramethyl ammoniumhydroxide

C3H6(2)HNO2

C3H6(2)HNO2

Conditions
ConditionsYield
In methanol at 0 - 20℃; for 2h;100%
tetramethyl ammoniumhydroxide
75-59-2

tetramethyl ammoniumhydroxide

carbonic acid dimethyl ester
616-38-6

carbonic acid dimethyl ester

tetramethylammonium methyl carbonate

tetramethylammonium methyl carbonate

Conditions
ConditionsYield
In methanol at 20℃; for 15h; Inert atmosphere;100%
In methanol for 16h; Inert atmosphere;99%
tetramethyl ammoniumhydroxide
75-59-2

tetramethyl ammoniumhydroxide

2,6-difluorobenzoic acid
385-00-2

2,6-difluorobenzoic acid

C7H3F2O2(1-)*C4H12N(1+)

C7H3F2O2(1-)*C4H12N(1+)

Conditions
ConditionsYield
With water In ethanol at 0 - 20℃; for 0.0833333h;100%
2,6-dimethylbenzoic acid
632-46-2

2,6-dimethylbenzoic acid

tetramethyl ammoniumhydroxide
75-59-2

tetramethyl ammoniumhydroxide

C9H9O2(1-)*C4H12N(1+)

C9H9O2(1-)*C4H12N(1+)

Conditions
ConditionsYield
With water In ethanol at 0 - 20℃; for 0.0833333h;100%
2-6-dimethoxybenzoic acid
1466-76-8

2-6-dimethoxybenzoic acid

tetramethyl ammoniumhydroxide
75-59-2

tetramethyl ammoniumhydroxide

C9H9O4(1-)*C4H12N(1+)

C9H9O4(1-)*C4H12N(1+)

Conditions
ConditionsYield
With water In ethanol at 0 - 20℃; for 0.0833333h;100%
Pentafluorobenzoic acid
602-94-8

Pentafluorobenzoic acid

tetramethyl ammoniumhydroxide
75-59-2

tetramethyl ammoniumhydroxide

C7F5O2(1-)*C4H12N(1+)

C7F5O2(1-)*C4H12N(1+)

Conditions
ConditionsYield
With water In ethanol at 0 - 20℃; for 0.0833333h;100%
4-trifluoromethylbenzoic acid
455-24-3

4-trifluoromethylbenzoic acid

tetramethyl ammoniumhydroxide
75-59-2

tetramethyl ammoniumhydroxide

C8H4F3O2(1-)*C4H12N(1+)

C8H4F3O2(1-)*C4H12N(1+)

Conditions
ConditionsYield
With water In ethanol at 0 - 20℃; for 0.0833333h;100%
4-(cyanomethyl)benzoic acid
50685-26-2

4-(cyanomethyl)benzoic acid

tetramethyl ammoniumhydroxide
75-59-2

tetramethyl ammoniumhydroxide

C9H6NO2(1-)*C4H12N(1+)

C9H6NO2(1-)*C4H12N(1+)

Conditions
ConditionsYield
With water In ethanol at 0 - 20℃; for 0.0833333h;100%
benzoic acid-2,3,4,5,6-d5
1079-02-3

benzoic acid-2,3,4,5,6-d5

tetramethyl ammoniumhydroxide
75-59-2

tetramethyl ammoniumhydroxide

C7(2)H5O2(1-)*C4H12N(1+)

C7(2)H5O2(1-)*C4H12N(1+)

Conditions
ConditionsYield
With water In ethanol at 0 - 20℃; for 0.0833333h;100%
4-Fluorobenzoic acid
456-22-4

4-Fluorobenzoic acid

tetramethyl ammoniumhydroxide
75-59-2

tetramethyl ammoniumhydroxide

tetramethylammonium 4-fluorobenzoate

tetramethylammonium 4-fluorobenzoate

Conditions
ConditionsYield
With water In ethanol at 0 - 20℃; for 0.0833333h;100%
In methanol at 20℃; for 16h; Inert atmosphere; Glovebox;82%
tetramethyl ammoniumhydroxide
75-59-2

tetramethyl ammoniumhydroxide

p-Toluic acid
99-94-5

p-Toluic acid

tetramethyl-ammonium; 4-methyl-benzoate

tetramethyl-ammonium; 4-methyl-benzoate

Conditions
ConditionsYield
With water In ethanol at 0 - 20℃; for 0.0833333h;100%
tetramethyl ammoniumhydroxide
75-59-2

tetramethyl ammoniumhydroxide

4-trifluoromethoxybenzoic acid
330-12-1

4-trifluoromethoxybenzoic acid

C8H4F3O3(1-)*C4H12N(1+)

C8H4F3O3(1-)*C4H12N(1+)

Conditions
ConditionsYield
With water In ethanol at 0 - 20℃; for 0.0833333h;100%
4-(ethoxy)benzoic acid
619-86-3

4-(ethoxy)benzoic acid

tetramethyl ammoniumhydroxide
75-59-2

tetramethyl ammoniumhydroxide

C9H9O3(1-)*C4H12N(1+)

C9H9O3(1-)*C4H12N(1+)

Conditions
ConditionsYield
With water In ethanol at 0 - 20℃; for 0.0833333h;100%
tetramethyl ammoniumhydroxide
75-59-2

tetramethyl ammoniumhydroxide

4-methoxybenzoic acid
100-09-4

4-methoxybenzoic acid

tetramethylammonium 4-methoxybenzoate
111536-98-2

tetramethylammonium 4-methoxybenzoate

Conditions
ConditionsYield
With water In ethanol at 0 - 20℃; for 0.0833333h;100%
4-Phenoxybenzoic acid
2215-77-2

4-Phenoxybenzoic acid

tetramethyl ammoniumhydroxide
75-59-2

tetramethyl ammoniumhydroxide

C13H9O3(1-)*C4H12N(1+)

C13H9O3(1-)*C4H12N(1+)

Conditions
ConditionsYield
With water In ethanol at 0 - 20℃; for 0.0833333h;100%
tetramethyl ammoniumhydroxide
75-59-2

tetramethyl ammoniumhydroxide

4-(1,1-dimethylethyl)benzoic acid
98-73-7

4-(1,1-dimethylethyl)benzoic acid

C11H13O2(1-)*C4H12N(1+)

C11H13O2(1-)*C4H12N(1+)

Conditions
ConditionsYield
With water In ethanol at 0 - 20℃; for 0.0833333h;100%
2-hydroxypyridin
142-08-5

2-hydroxypyridin

tetramethyl ammoniumhydroxide
75-59-2

tetramethyl ammoniumhydroxide

C5H4NO(1-)*C4H12N(1+)

C5H4NO(1-)*C4H12N(1+)

Conditions
ConditionsYield
In ethanol; water at 20℃; for 24h;100%
tetramethyl ammoniumhydroxide
75-59-2

tetramethyl ammoniumhydroxide

N,N,N',N'-Tetramethylphosphorodiamidic chloride
1605-65-8

N,N,N',N'-Tetramethylphosphorodiamidic chloride

A

tetramethylammonium bis(dimethylamino)phosphate
93048-79-4

tetramethylammonium bis(dimethylamino)phosphate

B

tetramethlyammonium chloride
75-57-0

tetramethlyammonium chloride

Conditions
ConditionsYield
In water for 3h;A 99.5%
B n/a
tetramethyl ammoniumhydroxide
75-59-2

tetramethyl ammoniumhydroxide

5-methyl-dihydro-furan-2-one
108-29-2

5-methyl-dihydro-furan-2-one

tetramethylammonium 4-hydroxyvalerate
1211890-38-8

tetramethylammonium 4-hydroxyvalerate

Conditions
ConditionsYield
In water for 1h;99.5%

75-59-2Relevant articles and documents

Synthesis method of N-hydroxymethyl acrylamide

-

Paragraph 0033-0035, (2021/06/12)

The invention relates to a synthesis method of N-hydroxymethyl acrylamide. By taking solid acrylamide and paraformaldehyde as raw materials, adopting a supported quaternary ammonium base catalyst, and selectively activating an amino group in the acrylamide by controlling the size of a hydrocarbyl group connected with quaternary ammonium base and utilizing the steric effect of hydrocarbyl, the self-polymerization behavior in the production process of the N-hydroxymethyl acrylamide is reduced, and the N-hydroxymethyl acrylamide monomer is efficiently obtained. The supported quaternary ammonium alkali is used as the catalyst, the reaction condition is mild, the selectivity is high, system polymerization caused by the traditional inorganic alkali liquor reaction is effectively avoided, and the reaction system can realize high-efficiency conversion of raw materials without adding a large amount of water as a reaction solvent, so that the yield is improved; and the supported quaternary ammonium base catalyst has the characteristics of large specific surface area, high reaction activity and the like, greatly reduces the use amount of solvent water in the reaction process, is convenient to remove in the post-treatment process, and reduces sewage discharge.

Quaternary ammonium salt type perrhenate ionic liquid and synthetic method and application thereof

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Paragraph 0022, (2017/06/02)

The invention discloses quaternary ammonium salt type perrhenate ionic liquid and a synthetic method and application thereof. The method comprises the steps that alkyl ammonium bromide and KOH are reacted to obtain quaternary ammonium base, the quaternary ammonium base and perrhenate (NH4ReO4) metal salt are subjected to a replacement reaction, and quaternary ammonium salt type perrhenate ionic liquid is obtained. The synthesized quaternary ammonium salt type perrhenate ionic liquid is a pollution-free catalyst, has catalysis activity for lignocellulose, can be used as the catalyst for degrading lignocellulose to prepare reducing sugar, and the high yield is obtained.

Temperature effect on the molecular interactions between ammonium ionic liquids and N, N-dimethylformamide

Attri, Pankaj,Venkatesu, Pannuru,Kumar, Anil

experimental part, p. 13415 - 13425 (2011/02/18)

In view of the wide scope of molecular interactions between the highly polar compound of N,N-dimethylformamide (DMF) and ammonium ionic liquids (ILs), we have measured thermophysical properties such as densities (??) and ultrasonic sound velocities (u) over the whole composition range at temperatures ranging from 25 to 50 ?°C under atmospheric pressure. To gain some insight into the several aggregations of molecular interactions present in these mixed solvents, we predicted the excess molar volume (VE) and the deviations in isentropic compressibilities (??Ks) as a function of the concentration of IL. These results are fitted to the Redlich-Kister polynomials. The materials investigated in the present study included the hydroxide series of ammonium ILs of tetramethylammonium hydroxide [(CH 3)4N][OH] (TMAH), tetraethylammonium hydroxide [(C 2H5)4N][OH] (TEAH), and tetrapropylammonium hydroxide [(C2H7)4N][OH] (TPAH). The intermolecular interactions and structural effects were analyzed on the basis of the measured and the derived properties. A qualitative analysis of the results is discussed in terms of the ion-dipole and ion-pair interactions, and hydrogen bonding between ILs and DMF molecules and their structural factors. ? 2010 American Chemical Society.

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