Lipase Basic Product Information

Product Name	Lipase	CAS	9001-62-1
Synonyms	ABSFungal Lipase L;Lipase PF;Lipase PL 266;Lipase PLG;Lipase PN;Lipase PS;Lipase PS Amano SD;Acid lipase;Adipose triglyceride lipase;Alfamalt LP 10066;Allzyme Lipase;Altus 13;Altus 2;Amano AP;Amano AY 1;Amano B;Amano CE;Amano CES;Amano I;Amano II;Amano LPL 200S;Amano M;Amano N-AP;Amano P;Amano PS 30;Arthrobacter lipase;Bakezyme PH 800;Bile salt-activated lipase;Bioprase OP 10;Butyrinase;Buzyme 2517;Cacordase;Capalase;Capalase K;Capalase L;Cartazyme LP;Chirazyme 435;Chirazyme L;Chirazyme L 1;Chirazyme L 10;Chirazyme L 2;Chirazyme L2C2;Chirazyme L 3;Chirazyme L 5;Chirazyme L 6;Chirazyme L 7;Chirazyme L 8;Chirazyme L 9;Chirazyme c-f;ChiroCLEC-CAB;ChiroCLEC-CR;ChiroCLEC-PC;Cleanase NLA-P;CloneZyme ESL 001;E.C.3.1.1.3;Enzylon PF;Fetipase;Fluozim G 3Kh;GA 56;GA 56(enzyme);Glycerol ester hydrolase;Greasex;Greasex 100L;ICR-107;ICR-113;Italase;Italase C;Lilipase A 10;Lilipase A 10FG;Lilipase A 5;Lilipase B 2;Lillipase A-10FG;Lipase;Lipase A;Lipase A 100L;Lipase A 10FG;Lipase AH;Lipase AK Amano;Lipase AKG;Lipase ALC;Lipase ALG;Lipase AP;Lipase AS;Lipase AY;Lipase AY 30;Lipase AY Amano 6;Lipase CE;Lipase CR;Lipase D Amano 2000;Lipase D Amano 350;Lipase EU-034;Lipase GC Amano 4;Lipase L Amano 10;Lipase LAK;Lipase LP;Lipase LP 'S';Lipase M 10;Lipase M-AP 10;Lipase MY;Lipase OF;Lipase OFEX;Lipase PA;	Molecular Formula	Unspecified
EINECS Number	232-619-9	Molecular Structure
Appearance	Light Yellow Powder
Purity	AR 98%
Supply Ability

Lipase Quality documents

Lipase Appearance/Package/Shipping/Storage

package

storage condition

Store in cool & dry place,Keep away from strong light and heat

Lipase Application

Lipase literature

Method for preparing optically active 5-hydroxy-3-(4'-hydroxyphenyl)-1,1,3-trimethylindane

-

, (2008/06/13)

A process for resolving racemic diesters of (R,S)(±)-5-hydroxy-3-(4'-hydroxyphenyl)-1,1,3-trimethylindane is disclosed. The process utilizes a microbial enzyme derived from Chromobacterium viscosum to catalyze the enantioselective and regioselective hydrolysis of the (S)(-)-enantiomer of the racemic mixture to its corresponding monoester at a faster rate than the (R)(+)-enantiomer. A substantially pure (S)(-)-indane monoester is thereby formed, while the (R)(+)-indane diester remains unreacted. The (S)(-)-monoester and the (R)(+)-diester can then be hydrolyzed using conventional techniques to form optically active (R)(+)- and (S)(-)-5-hydroxy-3-(4'-hydroxyphenyl)-1,1,3-trimethylindane enantiomers for use as monomers in the synthesis of chiral polymers.

Optical resolution for producing optically active alcohol

-

, (2008/06/13)

A process for producing an optically active alcohol comprising carrying out interesterification between a racemic alcohol and an ester selected from the group consisting of (a) a diester between a lower monohydric alcohol and a saturated dicarboxylic acid having 14 or more carbon atoms, (b) a triglyceride of a saturated fatty acid having 16 or more carbon atoms, and (c) a monoester between a lower monohydric alcohol and a saturated fatty acid having 18 or more carbon atoms in the presence of lipase, preferably heat-resistant lipase, and in the presence or absence of a solvent, preferably in the absence of a solvent, under a substantially water-free condition, separating an optically active alcohol rich in either one of R- and S-forms from the reaction mixture, and adding an optically inactive non-racemic alcohol to the residue of the previous step to carry out interesterification under the same conditions as in the previous reaction to separate the other enantiomer. According to the present invention a racemic alcohol can easily be resolved into each enantiomer with high purity in good yield.

Lipase Upstream and downstream

9001-62-1 Upstream product

9001-62-1 Downstream Products

• 106-05-8

  isooctyl palmitate 

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