Fucoxanthin

Basic information

  • Product Name:Fucoxanthin
  • CasNo.:3351-86-8
  • MF:C42H58O6
  • MW:658.919

Physical and Chemical Properties

  • Purity:99%
  • Boiling Point:166-168 °C
  • Packing:Crystalline solid
  • Throughput:
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Product Details

CasNo: 3351-86-8

MF: C42H58O6

Appearance: Crystalline solid

Good factory supply good Fucoxanthin 3351-86-8

  • Molecular Formula:C42H58O6
  • Molecular Weight:658.919
  • Appearance/Colour:Crystalline solid 
  • Melting Point:166-168 °C 
  • Refractive Index:1.563 
  • Boiling Point:764.1 °C at 760 mmHg 
  • PKA:14.47±0.60(Predicted) 
  • Flash Point:223 °C 
  • PSA:96.36000 
  • Density:1.09 g/cm3 
  • LogP:8.69220 

Fucoxanthin(Cas 3351-86-8) Usage

Biochem/physiol Actions

Xanthophyll carotenoid pigment extracted from algae. Exhibits anticancer, antioxidant, anti-obesity and anti-inflammatory properties.

Definition

ChEBI: A natural product found in Sporochnus comosus.

General Description

Fucoxanthin is isolated from brown algae. It has anti-angiogenic, hepatoprotective,?cardiovascular and cerebrovascular protective properties. Fucoxanthin stimulates G1 cell-cycle arrest and apoptosis in cancer cell lines.

InChI:InChI=1/C42H60O7/c1-29(18-14-19-31(3)22-23-37-38(6,7)26-35(49-33(5)43)27-40(37,10)46)16-12-13-17-30(2)20-15-21-32(4)36(45)28-42(48)39(8,9)24-34(44)25-41(42,11)47/h12-22,34-35,44,46-48H,24-28H2,1-11H3/b13-12+,18-14+,20-15+,29-16+,30-17+,31-19+,32-21+/t23-,34-,35-,40+,41+,42-/m0/s1

3351-86-8 Relevant articles

Application of diphenyl diselenide as a new catalyst for photochemical stereoisomerization of carotenoids

Strand, Aase,Liaaen-Jensen, Synnove

, p. 1263 - 1269 (2007/10/03)

In a comparative study, diphenyl diselen...

Carotenoids and related polyenes. Part 3. First total synthesis of fucoxanthin and halocynthiaxanthin using oxo-metallic catalyst

Yamano, Yumiko,Tode, Chisato,Ito, Masayoshi

, p. 1895 - 1904 (2007/10/02)

The first total synthesis of optically a...

Total synthesis of photosynthetic pigment fucoxanthin by use of oxo- metallic catalyst

Yamano,Ito

, p. 410 - 412 (2007/10/02)

The first total synthesis of optically a...

3351-86-8 Process route

Acetic acid (1S,3R)-3-hydroxy-4-[(3E,5E,7E,9E,11E,13E,15E)-18-((R)-4-hydroxy-2,6,6-trimethyl-cyclohex-1-enyl)-3,7,12,16-tetramethyl-17-oxo-octadeca-1,3,5,7,9,11,13,15-octaenylidene]-3,5,5-trimethyl-cyclohexyl ester

Acetic acid (1S,3R)-3-hydroxy-4-[(3E,5E,7E,9E,11E,13E,15E)-18-((R)-4-hydroxy-2,6,6-trimethyl-cyclohex-1-enyl)-3,7,12,16-tetramethyl-17-oxo-octadeca-1,3,5,7,9,11,13,15-octaenylidene]-3,5,5-trimethyl-cyclohexyl ester

fucoxanthin
3351-86-8,17257-05-5,55659-36-4,55659-37-5,55659-38-6,92761-37-0,124378-42-3,138126-73-5,141270-13-5,141270-14-6,141270-15-7,141270-16-8

fucoxanthin

Acetic acid (1S,3R)-3-hydroxy-4-[(3E,5E,7E,9E,11E,13E,15E)-18-((1R,4S,6S)-4-hydroxy-2,2,6-trimethyl-7-oxa-bicyclo[4.1.0]hept-1-yl)-3,7,12,16-tetramethyl-17-oxo-octadeca-1,3,5,7,9,11,13,15-octaenylidene]-3,5,5-trimethyl-cyclohexyl ester

Acetic acid (1S,3R)-3-hydroxy-4-[(3E,5E,7E,9E,11E,13E,15E)-18-((1R,4S,6S)-4-hydroxy-2,2,6-trimethyl-7-oxa-bicyclo[4.1.0]hept-1-yl)-3,7,12,16-tetramethyl-17-oxo-octadeca-1,3,5,7,9,11,13,15-octaenylidene]-3,5,5-trimethyl-cyclohexyl ester

Conditions
Conditions Yield
With 3-chloro-benzenecarboperoxoic acid;
28%
8%
With 3-chloro-benzenecarboperoxoic acid; In dichloromethane; at 0 ℃; for 1h; Yield given;
fucoxanthin
3351-86-8,17257-05-5,55659-36-4,55659-37-5,55659-38-6,92761-37-0,124378-42-3,138126-73-5,141270-13-5,141270-14-6,141270-15-7,141270-16-8

fucoxanthin

Conditions
Conditions Yield
With iodine; for 8h; Irradiation; sunlight;

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