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Chemical Structure| 22880-03-1 Chemical Structure| 22880-03-1
Chemical Structure| 22880-03-1

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Conjugated linoleic acid (CLA) is a bioactive fatty acid with anti-obesity and anti-cancer properties. It exhibits health benefits by regulating lipid metabolism and inflammatory responses.

4.5 *For Research Use Only! Not for Human Use. We Do Not Sell to Patients.

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Product Details of Conjugated Linoleic Acid

CAS No. :22880-03-1
Formula : C18H32O2
M.W : 280.45
SMILES Code : CCCCCC=CC=CCCCCCCCCC(O)=O
English Name :Octadeca-10,12-dienoic acid
MDL No. :N/A

Safety of Conjugated Linoleic Acid

Application In Synthesis of Conjugated Linoleic Acid

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 22880-03-1 ]

[ 22880-03-1 ] Synthesis Path-Downstream   1~5

  • 1
  • [ 60-33-3 ]
  • [ 1839-11-8 ]
  • [ 22880-03-1 ]
YieldReaction ConditionsOperation in experiment
With potassium hydroxide; ethylene glycol for 4h; Heating; Title compound not separated from byproducts;
  • 2
  • [ 57884-97-6 ]
  • [ 1839-11-8 ]
  • [ 22880-03-1 ]
YieldReaction ConditionsOperation in experiment
With potassium hydroxide In ethanol for 8h; Heating; Title compound not separated from byproducts;
  • 3
  • [ 141-22-0 ]
  • [ 22880-03-1 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 3 steps 1: BF3 / 1 h / 65 °C 2: 2.2 g / Et3N / CH2Cl2 / 0.75 h 3: KOH / ethanol / 8 h / Heating
  • 4
  • [ 141-24-2 ]
  • [ 22880-03-1 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: 2.2 g / Et3N / CH2Cl2 / 0.75 h 2: KOH / ethanol / 8 h / Heating
YieldReaction ConditionsOperation in experiment
With Lipozyme RM-IM at 65 - 110℃; for 36h; Enzymatic reaction; 3 Conjugated linoleic acid (110 lbs) and glycerol (20.8 lbs) were circulated through a packed column containing 2.9 lbs of Lipozyme RM-IM (Novozyme Co.). The column was maintained at 65 C. After exiting the column, the reaction mixture was heated to 110 C., then cooled and returned to the packed column for further reaction. Water of reaction was removed continually throughout the reaction. After about 36 hours, the reaction was complete
 

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