• Dimethyl Carbonate - DMC System 1
  • Dimethyl Carbonate - DMC System 2
  • Dimethyl Carbonate - DMC System 3
Dimethyl Carbonate - DMC

Dimethyl Carbonate - DMC

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Loading Port:
Qingdao
Payment Terms:
TT or LC
Min Order Qty:
-
Supply Capability:
6000吨 kg/month

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1.Brief Introduction

1.DMC is an inexpensive oxygenated solvent with excellent solubility properties, that can solve almost all coating resins.
2.DMC is now cheaper than MEK, Ethyl Acetate, MIBK, Butyl Acetate and most other Ketones and Glycol Ethers.

3.DMC is price competitive with acetone, toluene, ethanol and mineral spirits

4. DMC is VOC Exempt

 

2.Characteristics

 
Dimethyl Carbonate / DMC, CAS No.:616-38-6, chemical solvent
Dimethyl Carbonate 616-38-6
c3h6o3 Dimethyl Carbonate
price of Dimethyl Carbonate / DMC, CAS No.:616-38-6, chemical solvent

 

3.Product Specifications


Relative molecular weight : 90.08
CAS No.: 616-38-6 
UN No.: 1161 Class: 3.2

 

Item

Top class

First class

Appearance

Colorless&transparent liquid

Colorless&transparent liquid

Content

≥99.9%

≥99.5%

Methanol 

≤0.02%

≤0.1%

Moisture

≤0.02%

≤0.1%

Acidity (CH3COOH)

≤0.015%

≤0.015%

Free chlorine

≤0.01%

≤0.01%

Color (APHA)

≤5

≤10

 

4.FAQ

Packing and Storage:

Packaging

200kgs/drum,1000kg/IBC drum, ISO TANK

Delivery

15 days after receiving your deposit

 

 

 

Q: Derivatives of vinyl acetate
Vinyl acetate can produce reactions that occur most of the olefins or esters. Such as the addition of bromine to form dibromide, the addition of hydrogen halide to produce vinyl haloacetate, which is the only way to produce the substance because there is no corresponding halohydrin. The addition of acetic acid under palladium catalysis can produce ethylene diacetate and CH3CH (OAc) 2. The latter can undergo a transesterification reaction with many carboxylic acids. As an alkene, vinyl acetate can also undergo a Diels-Alder reaction and a 2 + 2 ring addition
Q: What is a derivative?
Derivative refers to a compound formed by the substitution of atoms or radicals in a parent compound molecule by other atoms or radicals, known as derivatives of the parent compound. Derivatives named, the general parent compound as the main body, with other groups as a substituent. Such as: halogenated hydrocarbons, alcohols, aldehydes, carboxylic acids can be seen as derivatives of hydrocarbons, because they are hydrogen atoms of hydrocarbons are replaced by halogen, hydroxyl, oxygen and other products
Q: The nature and use of cellulose derivatives
By replacing the reagent selection and process design, the product can be dissolved in water, dilute alkali solution or organic solvent, or have thermoplastic properties such as chemical fiber, film, film, plastic, insulating material, coating, slurry , Polymeric dispersants, food additives and household chemical products. The nature of the cellulose derivative and the nature of the substituent, the degree of substitution of the three hydroxyl groups on the glucose group, and the distribution of the substituents along the macromolecular chain. Due to the randomness of the reaction, the following three substitutions are different in other cases (homogeneous or heterogeneous reactions) except that the three hydroxyl groups are substituted (DS = 3) And non-substituted glucose groups: (1) monosubstituted (DS is 1, C, C or C position is substituted, the structural formula see cellulose); ② disubstituted (DS is 2, C, C, C, C Or C, C position is replaced); ③ total substitution (DS is 3). Thus, the properties of the same cellulose derivative having the same substitution value may also be quite different. For example, the cellulose diacetate which is directly esterified to DS of 2 is insoluble in acetone, but the cellulose diacetate obtained by saponification of the fully esterified cellulose triacetate can be completely dissolved in acetone. The irreducibility of this substitution is related to the basic rule of cellulose ester and etherification.

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