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Home ProductsDimethyl Succinate

Clear Dimethyl Succinate Dbe 4 Dimethyl Butanedioate 88.4 Degree Flash Point

Good quality Bio Based Succinic Acid for sales
Good quality Bio Based Succinic Acid for sales
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Clear Dimethyl Succinate Dbe 4 Dimethyl Butanedioate 88.4 Degree Flash Point

China Clear Dimethyl Succinate Dbe 4 Dimethyl Butanedioate 88.4 Degree Flash Point supplier

Large Image :  Clear Dimethyl Succinate Dbe 4 Dimethyl Butanedioate 88.4 Degree Flash Point

Product Details:

Place of Origin: China
Brand Name: Landian
Certification: SGS FDA

Payment & Shipping Terms:

Minimum Order Quantity: 0.5 tons
Price: Negotiation
Packaging Details: according to customers' requirements
Delivery Time: 1-3 working days
Supply Ability: 10000 tons/year
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Detailed Product Description
Cas No.: 106-65-0 Molecular Formula: C6H10O4
Molecular Weigh: 146.14 Port: Qingdao
Melting Point: 18-19℃ Flash Point: 88.4℃
High Light:

106 65 0

,

dimethyl butanedioate

 

Clear Dimethyl Succinate Dbe 4 Dimethyl Butanedioate 88.4 Degree Flash Point

 

name:dimethyl succinate

cas no.:106-65-0

molecular formula:c6h10o4

molecular weight:146.14

synonyms:butanedioicacid, dimethyl ester (9ci);succinic acid, dimethyl ester (6ci,8ci);dbe 4;dimethyl butanedioate;

einecs:203-419-9

density:1.086 g/cm3

melting point:18-19 °c

boiling point:195.3 °c at 760 mmhg

flash point:88.4 °c

 

Testing items Index Testing result
Appearance Colorless transparent liquid Colorless transparent liquid
Purity% ≥99.5 99.7
Water content% ≤0.1 0.06
acid value mgKOH/g ≤0.1 0.04
Color number(APHA) ≤20 10

 

Clear Dimethyl Succinate Dbe 4 Dimethyl Butanedioate 88.4 Degree Flash Point

The condensation of dimethyl succinate (I) with benzaldehyde (II) by means of NaOMe in refluxing methanol followed by hydrolysis with NaOH in methanol/water gives 2-benzylidenesuccinic acid (III). Compound (III) is treated with refluxing Ac2O, yielding the corresponding anhydride (IV), which by reaction with cis-perhydroisoindole (V) in toluene affords the monoamide (VI). This amide is reduced with H2 over a chiral Rhodium catalyst and treated with (R)-1-phenylethylamine (VII) to provide the chiral salt (VIII) as a single diastereomer isolated by crystallization. Finally, this salt is treated first with aqueous NH4OH and then with aqueous CaCl2.

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