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112-73-2

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112-73-2 Usage

Chemical Properties

clear colorless to yellowish liquid

Uses

Different sources of media describe the Uses of 112-73-2 differently. You can refer to the following data:
1. Butyl diglyme is used to extract gold from hydrochloric acid solutions containing other metals. Treatment of the diglyme extract with hydrogen or oxalic acid precipitates the ionic gold as gold powder.
2. Extraction of precious metalsDiethylene glycol dibutyl ether is used as a solvent in Grignard reactions. It is also used as solvents in gold refining, decorative inks for ceramics and digital inks. It finds application in electrochemistry, gas absorption, extractant and high boiling reaction medium. It is also used in fuel, lubricant, textile and medicine.

Reactivity Profile

Bis(2-butoxyethyl)ether may react violently with strong oxidizing agents. Incompatible with nitric acid. May form salts with strong acids and addition complexes with Lewis acids. In other reactions, which typically involve the breaking of the carbon-oxygen bond, relatively inert.

Health Hazard

May be harmful by inhalation, ingestion and skin absorption. Causes eye and skin irritation. Material is irritating to mucous membrane and upper respiratory tract.

Flammability and Explosibility

Nonflammable

Safety Profile

Moderately toxic by ingestion. Mddly toxic by skin contact. Experimental reproductive effects. A skin and eye irritant. See also GLYCOL ETHERS. Combustible when exposed to heat or flame. To fight fire, use foam or alcohol foam. When heated to decomposition it emits acrid smoke and irritating fumes.

Purification Methods

Dibutylcarbitol is freed from peroxides by slow passage through a column of activated alumina. The eluate is then shaken with Na2CO3 (to remove any remaining acidic impurities), washed with water, and stored with CaCl2 in a dark bottle [Tuck J Chem Soc 3202 1957]. [Beilstein 1 IV 2395.]

Check Digit Verification of cas no

The CAS Registry Mumber 112-73-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,1 and 2 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 112-73:
(5*1)+(4*1)+(3*2)+(2*7)+(1*3)=32
32 % 10 = 2
So 112-73-2 is a valid CAS Registry Number.
InChI:InChI:1S/C12H26O3/c1-3-5-7-13-9-11-15-12-10-14-8-6-4-2/h3-12H2,1-2H3

112-73-2 Well-known Company Product Price

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  • Alfa Aesar

  • (42150)  Diethylene glycol dibutyl ether, 99+%   

  • 112-73-2

  • 25ml

  • 203.0CNY

  • Detail
  • Alfa Aesar

  • (42150)  Diethylene glycol dibutyl ether, 99+%   

  • 112-73-2

  • 100ml

  • 478.0CNY

  • Detail
  • Alfa Aesar

  • (42150)  Diethylene glycol dibutyl ether, 99+%   

  • 112-73-2

  • 500ml

  • 2027.0CNY

  • Detail

112-73-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name Bis(2-butoxyethyl)ether

1.2 Other means of identification

Product number -
Other names Butane, 1,1‘-[oxybis(2,1-ethanediyloxy)]bis-

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Processing aids, not otherwise listed,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:112-73-2 SDS

112-73-2Synthetic route

n-Butyl chloride
109-69-3

n-Butyl chloride

diethylene glycol
111-46-6

diethylene glycol

diethylene glycol dibutyl ether
112-73-2

diethylene glycol dibutyl ether

Conditions
ConditionsYield
With sodium hydroxide; water; tetra(n-butyl)ammonium hydrogensulfate at 60℃; for 4h;97%
With perhydrodibenzo-18-crown-6; potassium hydroxide In water at 70℃; for 5h; Yield given;
1-chloro-hexan-3-ol
52418-81-2

1-chloro-hexan-3-ol

A

-butyl vinyl ether
111-34-2

-butyl vinyl ether

B

diethylene glycol dibutyl ether
112-73-2

diethylene glycol dibutyl ether

Conditions
ConditionsYield
With sodium hydroxide
1-(2-bromoethoxy)butane
6550-99-8

1-(2-bromoethoxy)butane

A

-butyl vinyl ether
111-34-2

-butyl vinyl ether

B

diethylene glycol dibutyl ether
112-73-2

diethylene glycol dibutyl ether

Conditions
ConditionsYield
With sodium hydroxide
3-oxa-1,5-dichloropentane
111-44-4

3-oxa-1,5-dichloropentane

sodium butanolate
2372-45-4

sodium butanolate

diethylene glycol dibutyl ether
112-73-2

diethylene glycol dibutyl ether

Conditions
ConditionsYield
With butan-1-ol
3-oxa-1,5-dichloropentane
111-44-4

3-oxa-1,5-dichloropentane

butan-1-ol
71-36-3

butan-1-ol

diethylene glycol dibutyl ether
112-73-2

diethylene glycol dibutyl ether

Conditions
ConditionsYield
With perhydrodibenzo-18-crown-6; potassium hydroxide In water Yield given;
1-bromo-butane
109-65-9

1-bromo-butane

diethylene glycol
111-46-6

diethylene glycol

diethylene glycol dibutyl ether
112-73-2

diethylene glycol dibutyl ether

Conditions
ConditionsYield
With perhydrodibenzo-18-crown-6; potassium hydroxide In water at 70℃; for 5h; Yield given;
1-(2-bromoethoxy)butane
6550-99-8

1-(2-bromoethoxy)butane

sodium hydroxide

sodium hydroxide

A

-butyl vinyl ether
111-34-2

-butyl vinyl ether

B

diethylene glycol dibutyl ether
112-73-2

diethylene glycol dibutyl ether

2-Butoxyethanol
111-76-2

2-Butoxyethanol

diethylene glycol dibutyl ether
112-73-2

diethylene glycol dibutyl ether

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: dimethylaniline; diethyl ether; PBr3
2: NaOH
View Scheme
1-bromo-butane
109-65-9

1-bromo-butane

Diethylene glycol monobutyl ether
112-34-5

Diethylene glycol monobutyl ether

diethylene glycol dibutyl ether
112-73-2

diethylene glycol dibutyl ether

Conditions
ConditionsYield
With sodium hydride In toluene at 50℃;
diethylene glycol dibutyl ether
112-73-2

diethylene glycol dibutyl ether

trityl azide
14309-25-2

trityl azide

N-(diphenylmethylidene)phenylamine
574-45-8

N-(diphenylmethylidene)phenylamine

Conditions
ConditionsYield
at 170 - 190℃; Rate constant;
diethylene glycol dibutyl ether
112-73-2

diethylene glycol dibutyl ether

hydrogen bromide
10035-10-6, 12258-64-9

hydrogen bromide

1-bromo-butane
109-65-9

1-bromo-butane

diethylene glycol dibutyl ether
112-73-2

diethylene glycol dibutyl ether

4-chloro-trityl azide
13189-73-6

4-chloro-trityl azide

x-chloro-benzophenone-phenylimine

x-chloro-benzophenone-phenylimine

Conditions
ConditionsYield
at 169.4℃; Rate constant;
at 179.8℃; Rate constant;
at 191℃; Rate constant;
diethylene glycol dibutyl ether
112-73-2

diethylene glycol dibutyl ether

4-methyl-trityl azide
13189-72-5

4-methyl-trityl azide

x-methyl-benzophenone-phenylimine

x-methyl-benzophenone-phenylimine

Conditions
ConditionsYield
at 170℃; Rate constant;
at 180℃; Rate constant;
at 191℃; Rate constant;
diethylene glycol dibutyl ether
112-73-2

diethylene glycol dibutyl ether

4-nitro-trityl azide
13189-74-7

4-nitro-trityl azide

x-nitro-benzophenone-phenylimine

x-nitro-benzophenone-phenylimine

Conditions
ConditionsYield
at 169.7℃; Rate constant;
at 179.8℃; Rate constant;
at 190.4℃; Rate constant;
diethylene glycol dibutyl ether
112-73-2

diethylene glycol dibutyl ether

ethyl 2-cyanoacrylate
7085-85-0

ethyl 2-cyanoacrylate

Co3(tris-(3-pyridyl)triazine)4(NCS)6

Co3(tris-(3-pyridyl)triazine)4(NCS)6

4C18H12N6*6CNS(1-)*3Co(2+)*2C6H7NO2*4C12H26O3

4C18H12N6*6CNS(1-)*3Co(2+)*2C6H7NO2*4C12H26O3

Conditions
ConditionsYield
Stage #1: Co3(tris-(3-pyridyl)triazine)4(NCS)6 In diethyl ether at 20℃; for 72h;
Stage #2: diethylene glycol dibutyl ether In diethyl ether at 20℃; under 2.8 Torr; Molecular sieve;
Stage #3: ethyl-2-cyanoacrilate at 4℃; for 48h; Inert atmosphere;

112-73-2Relevant articles and documents

Process for the preparation of cyclic esters and method for purification of the same

-

Page/Page column 11, (2010/11/30)

The present invention provides a process for production of a cyclic ester by depolymerization of an aliphatic polyester. In the process, a mixture containing the aliphatic polyester and a specific polyalkylene glycol ether, which has a boiling point of 230-450° C. and a molecular weight of 150-450, is heated under normal or reduced pressure to a temperature at which depolymerization of the aliphatic polyester takes place. Then, a substantially homogeneous solution phase, consisting of the melt phase of the aliphatic polyester and the liquid phase of the polyalkylene glycol ether, is formed. Heating of the solution phase is continued to form the cyclic ester by depolymerization and distil out the cyclic ester together with the polyalkylene glycol ether, and then the cyclic ester is recovered from the distillate. The present invention also provides a process for purification of a crude cyclic ester by use of the specific polyalkylene glycol ether described above.

CROWN ETHERS AS PHASE TRANSFER CATALYSTS IN EXTRACTIVE ALKYLATION REACTIONS

Tsarenko, N. A.,Yakshin, V. V.,Zhukova, N. G.,Laskorin, B. N.

, p. 215 - 217 (2007/10/02)

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