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143-22-6

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143-22-6 Usage

Chemical Properties

colourless to faintly yellow liquid

Uses

Different sources of media describe the Uses of 143-22-6 differently. You can refer to the following data:
1. Plasticizer, intermediate.
2. Triethylene glycol monobutyl ether, glycol ether a highly effective carrier solvent for textile dye processes. With superior surface tension characteristics, water solubility and solvency for oils, it has potential for use in household, institutional, industrial and special-purpose cleaners. The coupling ability of this product enhances performance and improves shelf stability of cleaning products. It is also used as an active solvent for solvent-based coatings, dye carrier for textile dye processes, coupling agent and solvent in household and industrial cleaners, paint and floor polish strippers, hard surface cleaners, and disinfectants, chemical process solvent and intermediate for ester production used as solvents, surfactants and plasticizers, coupling agent for resins and dyes in water-based printing ink, component of high-boiling hydraulic brake fluids.
3. Triethylene glycol monobutyl ether (TEGMBE) can be used as a solvent:In the synthesis of superparamagnetic iron oxide nanoparticles by thermal decomposition method.in the removal of CO2 due to its solubilize CO2.It can also be used as a reactant in the preparation of polyether adducts of bis(1,1,1,5,5,5-hexafluoro-2,4-pentanedionato)barium.

Flammability and Explosibility

Nonflammable

Check Digit Verification of cas no

The CAS Registry Mumber 143-22-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,4 and 3 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 143-22:
(5*1)+(4*4)+(3*3)+(2*2)+(1*2)=36
36 % 10 = 6
So 143-22-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H22O4/c1-2-3-5-12-7-9-14-10-8-13-6-4-11/h11H,2-10H2,1H3

143-22-6 Well-known Company Product Price

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  • Alfa Aesar

  • (L04738)  Triethylene glycol monobutyl ether, 98%   

  • 143-22-6

  • 250g

  • 322.0CNY

  • Detail
  • Alfa Aesar

  • (L04738)  Triethylene glycol monobutyl ether, 98%   

  • 143-22-6

  • 1000g

  • 846.0CNY

  • Detail

143-22-6SDS

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 Triethylene Glycol Monobutyl Ether

1.2 Other means of identification

Product number -
Other names Triethylene glycol monobutyl ether

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Fuels and fuel additives,Functional fluids (closed systems),Functional fluids (open systems),Processing aids, specific to petroleum production,Solvents (which become part of product formulation or mixture)
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:143-22-6 SDS

143-22-6Synthetic route

oxirane
75-21-8

oxirane

butan-1-ol
71-36-3

butan-1-ol

triethyleneglycol monobutyl ether
143-22-6

triethyleneglycol monobutyl ether

Conditions
ConditionsYield
With boron trifluoride diethyl etherate at 50℃;
With sodium
oxirane
75-21-8

oxirane

butan-1-ol
71-36-3

butan-1-ol

A

2-Butoxyethanol
111-76-2

2-Butoxyethanol

B

Diethylene glycol monobutyl ether
112-34-5

Diethylene glycol monobutyl ether

C

triethyleneglycol monobutyl ether
143-22-6

triethyleneglycol monobutyl ether

Conditions
ConditionsYield
2,4,6-trimethyl-pyridine at 160℃; under 2311.54 - 3345.86 Torr; for 2.5h; Product distribution / selectivity; Inert atmosphere;
sodium butanolate at 140℃; under 7500.75 Torr; for 5h; Product distribution / selectivity;A 20.16 %Chromat.
B 9.07 %Chromat.
C 6.10 %Chromat.
catalyst of invention (Sb2O3, copper acetate, hydrogen peroxide; calcined) at 140℃; under 30003 Torr; for 24 - 120h; Product distribution / selectivity;A 76 - 77 %Chromat.
B 13 - 14 %Chromat.
C 9 %Chromat.
Tetraethylene glycol
112-60-7

Tetraethylene glycol

ethylene glycol
107-21-1

ethylene glycol

butyraldehyde
123-72-8

butyraldehyde

diethylene glycol
111-46-6

diethylene glycol

2,2'-[1,2-ethanediylbis(oxy)]bisethanol
112-27-6

2,2'-[1,2-ethanediylbis(oxy)]bisethanol

A

2-propyl-1,3-dioxolane
3390-13-4

2-propyl-1,3-dioxolane

B

2-Butoxyethanol
111-76-2

2-Butoxyethanol

C

Diethylene glycol monobutyl ether
112-34-5

Diethylene glycol monobutyl ether

D

triethyleneglycol monobutyl ether
143-22-6

triethyleneglycol monobutyl ether

E

tetraethylene glycol monobutyl ether
1559-34-8

tetraethylene glycol monobutyl ether

F

butan-1-ol
71-36-3

butan-1-ol

Conditions
ConditionsYield
With hydrogen; palladium 10% on activated carbon at 180℃; under 51716.2 Torr; for 2h;
triethyleneglycol monobutyl ether
143-22-6

triethyleneglycol monobutyl ether

p-toluenesulfonyl chloride
98-59-9

p-toluenesulfonyl chloride

triethylene glycol monobutyl ether tosylate
117783-11-6

triethylene glycol monobutyl ether tosylate

Conditions
ConditionsYield
Stage #1: triethyleneglycol monobutyl ether; p-toluenesulfonyl chloride With dmap In dichloromethane at 20℃;
Stage #2: With triethylamine In dichloromethane at 20℃;
100%
With sodium hydroxide In tetrahydrofuran; water at 0℃; for 2h;83%
With sodium hydroxide In tetrahydrofuran; water at 0℃; for 4h;83%
triethyleneglycol monobutyl ether
143-22-6

triethyleneglycol monobutyl ether

methanesulfonyl chloride
124-63-0

methanesulfonyl chloride

triethyleneglycol monobutyl ether methanesulfonate
686289-90-7

triethyleneglycol monobutyl ether methanesulfonate

Conditions
ConditionsYield
With pyridine at 0℃; for 4h;96%
triethyleneglycol monobutyl ether
143-22-6

triethyleneglycol monobutyl ether

1,3-Diiodobenzene
626-00-6

1,3-Diiodobenzene

1,3-bis(2-(2-(2-butoxyethoxy)ethoxy)ethoxy)benzene

1,3-bis(2-(2-(2-butoxyethoxy)ethoxy)ethoxy)benzene

Conditions
ConditionsYield
With copper(l) iodide; 1,10-Phenanthroline; caesium carbonate In 5,5-dimethyl-1,3-cyclohexadiene for 20h; Reflux; Inert atmosphere;95%
triethyleneglycol monobutyl ether
143-22-6

triethyleneglycol monobutyl ether

1,2-Diiodobenzene
615-42-9

1,2-Diiodobenzene

1,2-bis(2-(2-(2-butoxyethoxy)ethoxy)ethoxy)benzene

1,2-bis(2-(2-(2-butoxyethoxy)ethoxy)ethoxy)benzene

Conditions
ConditionsYield
With copper(l) iodide; 1,10-Phenanthroline; caesium carbonate In 5,5-dimethyl-1,3-cyclohexadiene for 20h; Reflux; Inert atmosphere;68%
triethyleneglycol monobutyl ether
143-22-6

triethyleneglycol monobutyl ether

3-{[(4-bromobutyl)oxy]methyl}-3-methyloxetane
103781-33-5

3-{[(4-bromobutyl)oxy]methyl}-3-methyloxetane

3-(2,7,10,13,16-pentaoxaicosyl)-3-methyloxetane

3-(2,7,10,13,16-pentaoxaicosyl)-3-methyloxetane

Conditions
ConditionsYield
With sodium hydroxide; tetrabutylammomium bromide In hexane for 5h; Heating;67%
2,3-Dichloro-1,4-naphthoquinone
117-80-6

2,3-Dichloro-1,4-naphthoquinone

triethyleneglycol monobutyl ether
143-22-6

triethyleneglycol monobutyl ether

C30H46O10

C30H46O10

Conditions
ConditionsYield
With NAH In tetrahydrofuran at 80℃; Inert atmosphere;67%
triethyleneglycol monobutyl ether
143-22-6

triethyleneglycol monobutyl ether

3,6,9-trioxatridecanoic acid
75427-76-8

3,6,9-trioxatridecanoic acid

Conditions
ConditionsYield
With potassium hydroxide; potassium permanganate In water for 12h; Ambient temperature;57%
L-glutamic acid
56-86-0

L-glutamic acid

triethyleneglycol monobutyl ether
143-22-6

triethyleneglycol monobutyl ether

1,5-bis({2-[2-(2-butoxyethoxy)ethoxy]ethyl}) (2S)-2-aminopentanedioate

1,5-bis({2-[2-(2-butoxyethoxy)ethoxy]ethyl}) (2S)-2-aminopentanedioate

Conditions
ConditionsYield
With toluene-4-sulfonic acid In toluene at 130℃; for 4h; Dean-Stark;51.97%
triethyleneglycol monobutyl ether
143-22-6

triethyleneglycol monobutyl ether

hexatriethylene glycol mono-butyl ether-cyclophosphazene
107839-32-7

hexatriethylene glycol mono-butyl ether-cyclophosphazene

Conditions
ConditionsYield
With 2,2,4,4,6,6-hexachloro-1,3,5-triaza-2,4,6-triphosphorine; sodium hydride In tetrahydrofuran for 48h; Heating;29%
With 2,2,4,4,6,6-hexachloro-1,3,5-triaza-2,4,6-triphosphorine; tetrabutylammomium bromide; sodium hydride In tetrahydrofuran Yield given;
formaldehyd
50-00-0

formaldehyd

triethyleneglycol monobutyl ether
143-22-6

triethyleneglycol monobutyl ether

1,19-dibutoxy-3,6,9,11,14,17-hexaoxa-nonadecane
71563-36-5

1,19-dibutoxy-3,6,9,11,14,17-hexaoxa-nonadecane

Conditions
ConditionsYield
With toluene-4-sulfonic acid
triethyleneglycol monobutyl ether
143-22-6

triethyleneglycol monobutyl ether

acetaldehyde
75-07-0

acetaldehyde

1,1-bis-{2-[2-(2-butoxy-ethoxy)-ethoxy]-ethoxy}-ethane
71563-37-6

1,1-bis-{2-[2-(2-butoxy-ethoxy)-ethoxy]-ethoxy}-ethane

Conditions
ConditionsYield
With toluene-4-sulfonic acid
oct-1-ene
111-66-0

oct-1-ene

triethyleneglycol monobutyl ether
143-22-6

triethyleneglycol monobutyl ether

A

1,2-dichlorooctane
21948-46-9, 72778-28-0

1,2-dichlorooctane

B

2-{2-[2-(2-Butoxy-ethoxy)-ethoxy]-ethoxy}-1-chloro-octane

2-{2-[2-(2-Butoxy-ethoxy)-ethoxy]-ethoxy}-1-chloro-octane

C

1-{2-[2-(2-Butoxy-ethoxy)-ethoxy]-ethoxy}-2-chloro-octane

1-{2-[2-(2-Butoxy-ethoxy)-ethoxy]-ethoxy}-2-chloro-octane

Conditions
ConditionsYield
With chlorine In dichloromethane at 10 - 20℃; for 0.25h; Title compound not separated from byproducts;
triethyleneglycol monobutyl ether
143-22-6

triethyleneglycol monobutyl ether

octakiscyclotetraphosphazatetraene

octakiscyclotetraphosphazatetraene

Conditions
ConditionsYield
With octachlorocyclotetraphosphazene; tetrabutylammomium bromide; sodium hydride 1.) THF, reflux, 6 h, 2.) THF, reflux, 2 days; Yield given. Multistep reaction;
triethyleneglycol monobutyl ether
143-22-6

triethyleneglycol monobutyl ether

L-phenylalanine
63-91-2

L-phenylalanine

toluene-4-sulfonic acid
104-15-4

toluene-4-sulfonic acid

(S)-2-Amino-3-phenyl-propionic acid 2-[2-(2-butoxy-ethoxy)-ethoxy]-ethyl ester; compound with toluene-4-sulfonic acid

(S)-2-Amino-3-phenyl-propionic acid 2-[2-(2-butoxy-ethoxy)-ethoxy]-ethyl ester; compound with toluene-4-sulfonic acid

Conditions
ConditionsYield
In benzene Heating;
triethyleneglycol monobutyl ether
143-22-6

triethyleneglycol monobutyl ether

A

1-{2-[2-(2-chloroethoxy)ethoxy]ethoxy}butane
52184-05-1

1-{2-[2-(2-chloroethoxy)ethoxy]ethoxy}butane

B

1-(2-{2-[2-(2-Chloro-ethoxy)-ethoxy]-ethoxy}-ethoxy)-butane
52184-06-2

1-(2-{2-[2-(2-Chloro-ethoxy)-ethoxy]-ethoxy}-ethoxy)-butane

Conditions
ConditionsYield
With tetrachloromethane; triphenylphosphine
2-chloropyridine
109-09-1

2-chloropyridine

triethyleneglycol monobutyl ether
143-22-6

triethyleneglycol monobutyl ether

carbon monoxide
201230-82-2

carbon monoxide

pyridine-2-carboxylic acid 2-[2-(2-butoxy-ethoxy)-ethoxy]-ethyl ester

pyridine-2-carboxylic acid 2-[2-(2-butoxy-ethoxy)-ethoxy]-ethyl ester

Conditions
ConditionsYield
With bis(benzonitrile)palladium(II) dichloride; 1,3-bis-(diphenylphosphino)propane; triethylamine In N,N-dimethyl-formamide at 130℃; under 18751.5 Torr; for 14h;
triethyleneglycol monobutyl ether
143-22-6

triethyleneglycol monobutyl ether

1-{2-[2-(2-chloroethoxy)ethoxy]ethoxy}butane
52184-05-1

1-{2-[2-(2-chloroethoxy)ethoxy]ethoxy}butane

Conditions
ConditionsYield
With tetrachloromethane; triphenylphosphine for 2h; Heating;
triethyleneglycol monobutyl ether
143-22-6

triethyleneglycol monobutyl ether

C34H56O6P2

C34H56O6P2

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: triphenylphoshine; carbon tetrachloride / 2 h / Heating
2: 85 percent / buthyllithium / hexane; tetrahydrofuran / cooling
View Scheme
Multi-step reaction with 2 steps
1: PPh3; CCl4
View Scheme
triethyleneglycol monobutyl ether
143-22-6

triethyleneglycol monobutyl ether

10-(3,6,9-trioxatridecyl)-1,4,7,10-tetraazacyclododecane-1,4,7-triacetic acid
686289-85-0

10-(3,6,9-trioxatridecyl)-1,4,7,10-tetraazacyclododecane-1,4,7-triacetic acid

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: 96 percent / pyridine / 4 h / 0 °C
2: 58 percent / Na2CO3 / acetonitrile / 72 h / Heating
3: 97 percent / TFA / 4 h / 20 °C
View Scheme
triethyleneglycol monobutyl ether
143-22-6

triethyleneglycol monobutyl ether

10-(3,6,9-trioxatridecyl)-1,4,7,10-tetraazacyclododecane-1,4,7-triacetic acid tris(1,1-dimethylethyl) ester
686289-91-8

10-(3,6,9-trioxatridecyl)-1,4,7,10-tetraazacyclododecane-1,4,7-triacetic acid tris(1,1-dimethylethyl) ester

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 96 percent / pyridine / 4 h / 0 °C
2: 58 percent / Na2CO3 / acetonitrile / 72 h / Heating
View Scheme
triethyleneglycol monobutyl ether
143-22-6

triethyleneglycol monobutyl ether

C38H64O8P2

C38H64O8P2

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: PPh3; CCl4
View Scheme
triethyleneglycol monobutyl ether
143-22-6

triethyleneglycol monobutyl ether

(S)-2-((S)-2-tert-Butoxycarbonylamino-4-methyl-pentanoylamino)-3-phenyl-propionic acid 2-[2-(2-butoxy-ethoxy)-ethoxy]-ethyl ester

(S)-2-((S)-2-tert-Butoxycarbonylamino-4-methyl-pentanoylamino)-3-phenyl-propionic acid 2-[2-(2-butoxy-ethoxy)-ethoxy]-ethyl ester

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: benzene / Heating
2: 1.) ethyl 2-ethoxy-1,2-dihydroquinoline-1-carboxylate, 2.) Et3N / 1.) CH2Cl2, 15 min, 2.) CH2Cl2
View Scheme
triethyleneglycol monobutyl ether
143-22-6

triethyleneglycol monobutyl ether

N-(2-hydroxyethylene)bis(3,6,9,12-tetraoxahexadecyl)amine

N-(2-hydroxyethylene)bis(3,6,9,12-tetraoxahexadecyl)amine

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: 83 percent / sodium hydroxide / H2O; tetrahydrofuran / 4 h / 0 °C
2: 41 percent / sodium hydride / tetrahydrofuran / 49 h / Ambient temperature
3: 98 percent / aqueous hydrochloric acid / methanol / 2 h / Ambient temperature
View Scheme
triethyleneglycol monobutyl ether
143-22-6

triethyleneglycol monobutyl ether

N-bis(3,6,9,12-tetraoxahexadecyl)amine

N-bis(3,6,9,12-tetraoxahexadecyl)amine

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 83 percent / sodium hydroxide / H2O; tetrahydrofuran / 4 h / 0 °C
2: 41 percent / sodium hydride / tetrahydrofuran / 49 h / Ambient temperature
View Scheme
triethyleneglycol monobutyl ether
143-22-6

triethyleneglycol monobutyl ether

3-Hydroxypropylenbis(3,6,9-trioxatridecanoat)
75427-89-3

3-Hydroxypropylenbis(3,6,9-trioxatridecanoat)

Conditions
ConditionsYield
Multi-step reaction with 4 steps
1: 57 percent / potassium hydroxide, potassium permanganate / H2O / 12 h / Ambient temperature
2: phosphorpentachloride / CHCl3 / 2 h / Heating
3: 60 percent / pyridine / tetrahydrofuran / 48 h / Ambient temperature
4: 95 percent / H2 / palladium / C (10percent) / tetrahydrofuran / 3 h / 30 - 40 °C / 2206.5 - 2942.03 Torr
View Scheme
triethyleneglycol monobutyl ether
143-22-6

triethyleneglycol monobutyl ether

3-Benzyloxypropylenbis(3,6,9-trioxatridecanoat)
75427-83-7

3-Benzyloxypropylenbis(3,6,9-trioxatridecanoat)

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: 57 percent / potassium hydroxide, potassium permanganate / H2O / 12 h / Ambient temperature
2: phosphorpentachloride / CHCl3 / 2 h / Heating
3: 60 percent / pyridine / tetrahydrofuran / 48 h / Ambient temperature
View Scheme
triethyleneglycol monobutyl ether
143-22-6

triethyleneglycol monobutyl ether

1,2,3-Propantriyltris(3,6,9-trioxatridecanoat)
75427-70-2

1,2,3-Propantriyltris(3,6,9-trioxatridecanoat)

Conditions
ConditionsYield
Multi-step reaction with 5 steps
1: 57 percent / potassium hydroxide, potassium permanganate / H2O / 12 h / Ambient temperature
2: phosphorpentachloride / CHCl3 / 2 h / Heating
3: 60 percent / pyridine / tetrahydrofuran / 48 h / Ambient temperature
4: 95 percent / H2 / palladium / C (10percent) / tetrahydrofuran / 3 h / 30 - 40 °C / 2206.5 - 2942.03 Torr
5: 55 percent / pyridine / tetrahydrofuran / 48 h / Ambient temperature
View Scheme
Multi-step reaction with 3 steps
1: 57 percent / potassium hydroxide, potassium permanganate / H2O / 12 h / Ambient temperature
2: phosphorpentachloride / CHCl3 / 2 h / Heating
3: 55 percent / pyridine / tetrahydrofuran / 48 h / Ambient temperature
View Scheme

143-22-6Related news

Use of TRIETHYLENE GLYCOL MONOBUTYL ETHER (cas 143-22-6) in synthesis of iron oxide nanoparticles09/28/2019

Superparamagnetic iron oxide nanoparticles were synthesized by thermal decomposition of iron–oleate complex using triethylene glycol monobutyl ether (TREGBE) as solvent for the first time for more mass of the nanoparticles. The effect of TREGBE on the properties of the nanoparticles was compare...detailed

143-22-6Relevant articles and documents

INHIBITORS OF HEPATITIS C VIRUS POLYMERASE

-

Paragraph 331; 332, (2016/10/11)

The present invention provides, among other things, compounds represented by the general Formula I: (I) and pharmaceutically acceptable salts thereof, wherein L and A (and further substituents) are as defined in classes and subclasses herein and compositions (e.g., pharmaceutical compositions) comprising such compounds, which compounds are useful as inhibitors of hepatitis C virus polymerase, and thus are useful, for example, as medicaments for the treatment of HCV infection.

HETEROCYCLIC AMINE CATALYST COMPOSITIONS FOR THE ALKOXYLATION OF ALCOHOLS TO GLYCOL ETHERS

-

Page/Page column 8-9, 11, (2009/12/05)

Glycol ethers are made by a process in which an alcohol, an alkylene oxide and a catalytic amount of an aromatic, heterocyclic amine catalyst are contacted under reactive conditions. Representative catalysis include substituted and unsubsiituted pyridines and imidazoles. The process uses known oxides and alcohols, and produces more mono- and di- adduct products than does a corresponding process using a caustic catalyst. Moreover, the process can be conducted at a lower reaction temperature than a corresponding process using a caustic catalyst without sacrificing oxide conversion rates yet producing fewer carfoony! impurities.

METHOD FOR PRODUCING MONOALKYLENE GLYCOL MONOETHER

-

Page/Page column 24-25, (2010/02/14)

The invention relates to a method for producing monoalkylene glycol monoether of general formulas (Ia) and (Ib), wherein a group R is hydrogen, a methyl-, ethyl-, propyl- or butyl group and R1 is a phenyl or a linear or branched C1-C10 alkyl group consisting in reacting an alcohol R1OH (II) with an alkylene oxide (III) in the presence of a heterogeneous catalyst in a liquid phase which contains in the form of a catalytically active agent at least one composition of formula (IV): M1pAnm x zH2O, wherein M1is hydrogen and/or one or several cations of IA, IIA, IIIA groups, a IVA, IB, IIB, IIIB, IVB, VB, VIB, VIIB or VIIIB lanthanide groups, An is an anion of formula [M2qOn(OH)2(3-n)], wherein M2 is at least one cationic element from a group of pnicogens As, Sb and Bi, the index q is a value equal to 1, the index n is a fractional or an integer number equal to or greater than 0 and strictly less than 3, z is equal to 0 or an integer or fractional number strictly greater than 0 and equal or less than 10, the index p is a value normalised to 1 and the index m is a number ranging from 1.2 to 8 stoichiometrically obtainable from the electric charge of one or several cations M1 and from the electric charge of an An anion taking in to account the index p whose value is normalised to 1 at a temperature ranging from a room temperature to 350 °C, at a pressure ranging from atmospheric pressure to 80 bar and at a molar ratio alcohol II/alkylene oxide III ranging from 3:1 to 15:1.

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