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112-07-2

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112-07-2 Usage

Chemical Properties

colourless to pale yellow liquid with a mild odour

Uses

Different sources of media describe the Uses of 112-07-2 differently. You can refer to the following data:
1. High-boiling solvent for nitrocellulose lacquers, epoxy resins, multicolor lacquers; filmcoalescing aid for polyvinyl acetate latex.
2. 2-n-Butoxyethyl acetate is used as a solvent for nitrocellulose lacquers, enamels, coating additives, epoxy resins, and varnishes. It is a film coalescing aid for polyvinyl acetate latex. Further, it stimulates the release of prostaglandin E(2), an arachidonic acid metabolite, in human epidermal keratinocytes. In addition to this, it serves as an ingredient in ink removers and spot removers.
3. 2-Butoxyethyl Acetate is used in preparation of anti-aging coating with wear resistance, waterproof and acid and alkali resistance.

General Description

Colorless liquid with a weak fruity odor. Floats and mixes slowly with water.

Air & Water Reactions

Water soluble.

Reactivity Profile

2-Butoxyethyl acetate is incompatible with the following: Oxidizers . 2-Butoxyethyl acetate is an ether-alcohol derivative. The ether being relatively unreactive. Flammable and/or toxic gases are generated by the combination of alcohols with alkali metals, nitrides, and strong reducing agents. They react with oxoacids and carboxylic acids to form esters plus water. Oxidizing agents convert alcohols to aldehydes or ketones. Alcohols exhibit both weak acid and weak base behavior. They may initiate the polymerization of isocyanates and epoxides.

Health Hazard

Inhalation of concentrated vapor may cause headache, nausea, dizziness. Liquid causes irritation of eyes and mild irritation of skin. Ingestion produces same symptoms as inhalation.

Flammability and Explosibility

Nonflammable

Safety Profile

Moderately toxic by ingestion and skin contact. Mild skin irritant. Flammable when exposed to heat, flame, or oxidizers. To fight fire, use alcohol foam. When heated to decomposition it emits acrid smoke and irritating fumes. See also ESTERS.

Purification Methods

Shake the ester with anhydrous Na2CO3, filter and distil it in a vacuum. Redistillation can then be carried out at atmospheric pressure. [Dunbar & Bolstad J Org Chem 21 1041 1956, Beilstein 2 IV 215.]

Check Digit Verification of cas no

The CAS Registry Mumber 112-07-2 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, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 112-07:
(5*1)+(4*1)+(3*2)+(2*0)+(1*7)=22
22 % 10 = 2
So 112-07-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H12O2.C2H6O2/c1-3-4-5-8-6(2)7;3-1-2-4/h3-5H2,1-2H3;3-4H,1-2H2

112-07-2 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (L09515)  2-n-Butoxyethyl acetate, 98%   

  • 112-07-2

  • 100ml

  • 217.0CNY

  • Detail
  • Alfa Aesar

  • (L09515)  2-n-Butoxyethyl acetate, 98%   

  • 112-07-2

  • 500ml

  • 342.0CNY

  • Detail
  • Alfa Aesar

  • (L09515)  2-n-Butoxyethyl acetate, 98%   

  • 112-07-2

  • 2500ml

  • 661.0CNY

  • Detail

112-07-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Butoxyethyl acetate

1.2 Other means of identification

Product number -
Other names 2-butoxyethanolacetate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Paint additives and coating additives not described by other categories,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:112-07-2 SDS

112-07-2Downstream Products

112-07-2Related news

Solubilities of CO2 capture absorbents 2-ethoxyethyl ether, 2-Butoxyethyl acetate (cas 112-07-2) and 2-(2-ethoxyethoxy)ethyl acetate08/20/2019

The isothermal synthetic method was used to measure CO2 solubilities in three high-boiling-point absorbents, such as 2-ethoxyethyl ether, 2-butoxyethyl acetate and 2-(2-ethoxyethoxy)ethyl acetate under pressures ranging from 0 to 1.3 MPa and temperatures ranging from 293.15 to 333.15 K. Henry&#x...detailed

112-07-2Relevant articles and documents

Dinuclear μ-alkylidene complexes of transition metals as models for the transformation of CH2X2 (X=Cl, Br, I) into malonic acid derivatives by double carbonylation reactions

Denise, B.,Navarre, D.,Rudler, H.,Daran, J. C.

, p. 273 - 289 (1989)

The carbonylation of the μ-alkylidene complexes Fe2(CO)8CH2 (1) and Pd2I2(PPh2CH2PPh2)2CH2 (2) has been studied under a variety of conditions.In the presence of an alcohol ROH, complex 1 gives mainly the acetate CH3CO2R, the product of monocarbonylation, whereas under the same conditions complex 2 gives the malonate CH2(CO2R)2, the product of dicarbonylation.The mechanisms of both reactions are discussed.From the fraction involving 1 a mononuclear complex resulting from the dimerization of ketene has been isolated, and its structure established by an X-ray diffraction study.Olefins such as ethene and norbornene are able to trap the ketene intermediate.The possible participation of such μ-alkylidene complexes in the direct transformation of CH2X2 (X=Cl, Br, I) into malonic acid derivatives is discussed.

Method of Fabricating Glycol Monoalkyl Ether Acetate Using Acidic Ionic Liquid Catalyst

-

Page/Page column 4, (2011/08/06)

A new method for fabricating glycol monoalkyl ether acetate (GMAEA) is provided. A Bronsted acidic ionic liquid is used. After some reactions, two layers of materials are formed. A product of GMAEA is obtained at the upper layer. The lower layer is the ionic liquid. Thus, the ionic liquid is reusable for re-fabricating the product. And, furthermore, waste acid is reduced.

Reusable and efficient polystyrene-supported acidic ionic liquid catalyst for esterifications

Xu, Zhenjin,Wan, Hui,Miao, Jinmei,Han, Mingjuan,Yang, Cao,Guan, Guofeng

experimental part, p. 152 - 157 (2011/01/05)

Polystyrene (PS)-supported 1-(propyl-3-sulfonate) imidazolium hydrosulfate acidic ionic liquid (PS-CH2-[SO3H-pIM][HSO4]) catalyst was prepared by supporting the ionic liquid onto highly cross-linked chloromethylated polystyrene (PS-CH2Cl). FT-IR, SEM and TG-DSC were employed to characterize the structure and property of the catalyst. Results suggested that acidic ionic liquid was supported onto the surface of PS-CH 2Cl by covalent bond. The original rough surface of PS-CH 2Cl was covered with acidic ionic liquid, forming a compact and thin surface layer, and its size had no obvious change. Moreover, the PS-CH 2-[SO3H-pIM][HSO4] catalyst showed a better thermal stability than that of PS-CH2Cl support. It also exhibited high catalytic activity for a series of esterifications. After the catalyst was reused for 13 times in the synthesis of n-butyl acetate, the yield only decreased 7.3%. A reaction mechanism of esterification over this new catalyst was proposed as well.

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