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(3S)-β-Cryptoxanthin

Base Information Edit
  • Chemical Name:(3S)-β-Cryptoxanthin
  • CAS No.:1200446-88-3
  • Molecular Formula:C40H56O
  • Molecular Weight:552.884
  • Hs Code.:
  • Mol file:1200446-88-3.mol
(3S)-β-Cryptoxanthin

Synonyms:(3S)-β-Cryptoxanthin;(3S)-β,β-Caroten-3-ol;ent-β-Cryptoxanthin

Suppliers and Price of (3S)-β-Cryptoxanthin
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • (3S)-β-Cryptoxanthin
  • 1mg
  • $ 440.00
Total 2 raw suppliers
Chemical Property of (3S)-β-Cryptoxanthin Edit
Chemical Property:
  • PSA:20.23000 
  • LogP:11.57660 
Purity/Quality:

97% *data from raw suppliers

(3S)-β-Cryptoxanthin *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Uses The R-enatiomer of (3S)-β-Cryptoxanthin (C827500), a natural caratenoid pigment that is an antioxidant which helps prevent free radical damage to cells and DNA as well as being a potential chemopreventative agent against lung cancer.
Technology Process of (3S)-β-Cryptoxanthin

There total 5 articles about (3S)-β-Cryptoxanthin which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With ethyloxirane; In ethanol; for 6h; optical yield given as %ee; Inert atmosphere; Reflux;
DOI:10.1055/s-0030-1258382
Guidance literature:
Multi-step reaction with 5 steps
1: potassium hydroxide / tetrahydrofuran; methanol / 1 h / 50 °C / Inert atmosphere
2: immobilized lipase Pseudomonas cepacia / ethyl acetate / 20 h / 20 °C / Inert atmosphere; Enzymatic reaction
3: tetrahydrofuran; toluene / 1.5 h / -20 °C / Inert atmosphere
4: methanol; water / 0 - 20 °C
5: ethyloxirane / ethanol / 6 h / Inert atmosphere; Reflux
With ethyloxirane; potassium hydroxide; In tetrahydrofuran; methanol; ethanol; water; ethyl acetate; toluene; 4: Wittig reaction;
DOI:10.1055/s-0030-1258382
Guidance literature:
Multi-step reaction with 2 steps
1: methanol; water / 0 - 20 °C
2: ethyloxirane / ethanol / 6 h / Inert atmosphere; Reflux
With ethyloxirane; In methanol; ethanol; water; 1: Wittig reaction;
DOI:10.1055/s-0030-1258382
Refernces Edit
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