Others
(3S,3'S,5R,5'R)-3,3'-dihydroxy-.kappa.,.kappa.-carotene-6,6'-dione
- CAS No.: 470-38-2
- Purity: 99%
Quality products?make an important contribution to long-term revenue and profitability. Offer Chemical Raw Material (3S,3'S,5R,5'R)-3,3'-dihydroxy-.kappa.,.kappa.-carotene-6,6'-dione 470-38-2 In Stock
1.What is the (3S,3'S,5R,5'R)-3,3'-dihydroxy-.kappa.,.kappa.-carotene-6,6'-dione ?
Capsorubin, is a carotenoid pigment. It is also a metabolite of a Xanthophyll (X742000) with a structure containing unusual five-membered ring end groups. It is found in red peppers (Capsicum annuum), which has shown to have Antioxidant, Antinociceptive, and Anti-inflammatory effects.
-
-
C33 H38 O2 P(1+) *Cl(1-)
-
-
336105-82-9
(2E,4E,6E,8E,10E,12E)-14[(1R,4S)-4-hydroxy-1,2,2-trimethylcyclopentyl]-2,7,11-trimethyl-14-oxotetradeca-2,4,6,8,10,12-hexaenal
-
-
470-38-2
capsorubin
| Conditions | Yield |
|---|---|
|
With
sodium methylate;
In
methanol;
at 20 ℃;
for 2h;
|
30%
|
-
-
87798-58-1
(R )-1,2,2-trimethyl-cyclopent-3-ene-1,3-dicarboxylic acid
-
-
470-38-2
capsorubin
| Conditions | Yield |
|---|---|
|
Multi-step reaction
with
8
steps
1: lithium bromide, hydrobromic acid / 100 °C
2: 55 percent / aq. sodium carbonate / Heating
4: 95 percent / 2N-sodium hydroxide / 1.5 h / Heating
5: 1.) 0.5N-hydrochloric acid, hydrogen / 1.)platinum dioxide / 1.) glacial acetic acid, 20 deg C, 30 h, 2.) ether
6: 7 mg / 2N sodium hydroxide / 2 h / Heating
7: 55 percent / diethyl ether / 18 h / Heating
8: potassium hydroxide / ethanol / 1.) 40 deg C, 5 min, 2.) in dark, 68 h
With
hydrogenchloride; potassium hydroxide; sodium hydroxide; hydrogen bromide; hydrogen; sodium carbonate; lithium bromide;
platinum(IV) oxide;
In
diethyl ether; ethanol;
|
|
|
Multi-step reaction
with
7
steps
1: lithium bromide, hydrobromic acid / 100 °C
2: 55 percent / aq. sodium carbonate / Heating
4: 95 percent / 2N-sodium hydroxide / 1.5 h / Heating
5: 1.30 g / 2N-sodium hydroxide, potassium borohydride / 17 h / Heating
6: 55 percent / diethyl ether / 18 h / Heating
7: potassium hydroxide / ethanol / 1.) 40 deg C, 5 min, 2.) in dark, 68 h
With
potassium hydroxide; sodium hydroxide; potassium borohydride; hydrogen bromide; sodium carbonate; lithium bromide;
In
diethyl ether; ethanol;
|
|
|
Multi-step reaction
with
7
steps
1: lithium bromide, hydrobromic acid / 100 °C
2: 55 percent / aq. sodium carbonate / Heating
4: 95 percent / 2N-sodium hydroxide / 1.5 h / Heating
5: 0.5N-sodium hydroxide, hydrogen / 5percent ruthenium on carbon / 65 h / 20 °C
6: 55 percent / diethyl ether / 18 h / Heating
7: potassium hydroxide / ethanol / 1.) 40 deg C, 5 min, 2.) in dark, 68 h
With
potassium hydroxide; sodium hydroxide; hydrogen bromide; hydrogen; sodium carbonate; lithium bromide;
ruthenium;
In
diethyl ether; ethanol;
|
|
|
Multi-step reaction
with
10
steps
1: lithium bromide, hydrobromic acid / 100 °C
2: 85 percent / aq. sodium carbonate / Heating
3: 1.65 g / 2N-sodium hydroxide / 1 h / Heating
4: diethyl ether
5: 1.) potassium dichromate, conc. sulphuric acid, 2.) acetic acid, hydrochloric acid / 1.) ether, water, 4 h, 2.) water, reflux, 7 h
6: 95 percent / 2N-sodium hydroxide / 1.5 h / Heating
7: 1.) 0.5N-hydrochloric acid, hydrogen / 1.)platinum dioxide / 1.) glacial acetic acid, 20 deg C, 30 h, 2.) ether
8: 7 mg / 2N sodium hydroxide / 2 h / Heating
9: 55 percent / diethyl ether / 18 h / Heating
10: potassium hydroxide / ethanol / 1.) 40 deg C, 5 min, 2.) in dark, 68 h
With
hydrogenchloride; potassium dichromate; potassium hydroxide; sodium hydroxide; sulfuric acid; hydrogen bromide; hydrogen; sodium carbonate; acetic acid; lithium bromide;
platinum(IV) oxide;
In
diethyl ether; ethanol;
|
|
|
Multi-step reaction
with
9
steps
1: lithium bromide, hydrobromic acid / 100 °C
2: 85 percent / aq. sodium carbonate / Heating
3: 1.65 g / 2N-sodium hydroxide / 1 h / Heating
4: diethyl ether
5: 1.) potassium dichromate, conc. sulphuric acid, 2.) acetic acid, hydrochloric acid / 1.) ether, water, 4 h, 2.) water, reflux, 7 h
6: 95 percent / 2N-sodium hydroxide / 1.5 h / Heating
7: 1.30 g / 2N-sodium hydroxide, potassium borohydride / 17 h / Heating
8: 55 percent / diethyl ether / 18 h / Heating
9: potassium hydroxide / ethanol / 1.) 40 deg C, 5 min, 2.) in dark, 68 h
With
hydrogenchloride; potassium dichromate; potassium hydroxide; sodium hydroxide; potassium borohydride; sulfuric acid; hydrogen bromide; sodium carbonate; acetic acid; lithium bromide;
In
diethyl ether; ethanol;
|
|
|
Multi-step reaction
with
9
steps
1: lithium bromide, hydrobromic acid / 100 °C
2: 85 percent / aq. sodium carbonate / Heating
3: 1.65 g / 2N-sodium hydroxide / 1 h / Heating
4: diethyl ether
5: 1.) potassium dichromate, conc. sulphuric acid, 2.) acetic acid, hydrochloric acid / 1.) ether, water, 4 h, 2.) water, reflux, 7 h
6: 95 percent / 2N-sodium hydroxide / 1.5 h / Heating
7: 0.5N-sodium hydroxide, hydrogen / 5percent ruthenium on carbon / 65 h / 20 °C
8: 55 percent / diethyl ether / 18 h / Heating
9: potassium hydroxide / ethanol / 1.) 40 deg C, 5 min, 2.) in dark, 68 h
With
hydrogenchloride; potassium dichromate; potassium hydroxide; sodium hydroxide; sulfuric acid; hydrogen bromide; hydrogen; sodium carbonate; acetic acid; lithium bromide;
ruthenium;
In
diethyl ether; ethanol;
|
2.What is the CAS number for (3S,3'S,5R,5'R)-3,3'-dihydroxy-.kappa.,.kappa.-carotene-6,6'-dione ?
The CAS number of (3S,3'S,5R,5'R)-3,3'-dihydroxy-.kappa.,.kappa.-carotene-6,6'-dione is 470-38-2.
More information of (3S,3'S,5R,5'R)-3,3'-dihydroxy-.kappa.,.kappa.-carotene-6,6'-dione 470-38-2 are:
|
CAS?Number |
470-38-2 |
|
Density |
1.016g/cm3 |
|
Melting Point |
201 °C |
|
Boiling Point |
741.8°Cat760mmHg |
|
Flash Point |
416.4°C |
|
PSA |
74.60000 |
|
LogP |
9.06520 |
|
Pka |
14.55±0.60(Predicted) |
3.What are another words for (3S,3'S,5R,5'R)-3,3'-dihydroxy-.kappa.,.kappa.-carotene-6,6'-dione ?
Synonyms?for?(3S,3'S,5R,5'R)-3,3'-dihydroxy-.kappa.,.kappa.-carotene-6,6'-dione 470-38-2:2,4,6,8,10,12,14,16,18-Eicosanonaene-1,20-dione,1,20-bis(4-hydroxy-1,2,2-trimethylcyclopentyl)-4,8,13,17-tetramethyl-,(1R,1R,4S,4S)-(all-E)- (8CI); Capsorubin; Capsorubin, all-trans-;all-trans-Capsorubin
4.What is the molecular formula of (3S,3'S,5R,5'R)-3,3'-dihydroxy-.kappa.,.kappa.-carotene-6,6'-dione?
The chemical formula of ?(3S,3'S,5R,5'R)-3,3'-dihydroxy-.kappa.,.kappa.-carotene-6,6'-dione is?C40H56 O4 which containing 40 Carbon atoms,56 Hydrogen atoms and 4 Oxygen atoms,and the molecular weight of??(3S,3'S,5R,5'R)-3,3'-dihydroxy-.kappa.,.kappa.-carotene-6,6'-dione?is 600.882.
5.What is (3S,3'S,5R,5'R)-3,3'-dihydroxy-.kappa.,.kappa.-carotene-6,6'-dione (470-38-2) used for?
(3S,3'S,5R,5'R)-3,3'-dihydroxy-.kappa.,.kappa.-carotene-6,6'-dione, also known as Capsorubin, is a carotenoid pigment and a metabolite of a Xanthophyll (X742000) with a unique structure containing unusual five-membered ring end groups. It is derived from red peppers (Capsicum annuum) and has been found to possess various beneficial properties, including antioxidant, antinociceptive, and anti-inflammatory effects.
Relevant articles related to (3S,3'S,5R,5'R)-3,3'-dihydroxy-.kappa.,.kappa.-carotene-6,6'-dione:
|
Article |
Source |
|
Kinetic Studies on the Thermal (Z/E)-Isomerization of C40-Carotenoids |
Molnar, Peter,Kortvelyesi, Tarnas,Matus, Zoltan,Szabolca, Jozsef , p. 801 - 841 (2007/10/03) |
|
Synthesis of optically active natural carotenoids and structurally related compounds. X. Synthesis of (3R,3'S,5'R)-capsanthin, 3S,5R,3'S,5'R)-capsorubin, (3'S,5'R)-cryptocapsin, and some related compounds. A new approach to optically active, five-membered-ring carotenoid building units by hydroboration |
Ruttimann,Engbert,Mayer,et al. , p. 1939 - 1960 (2007/10/02) |
6.Buy (3S,3'S,5R,5'R)-3,3'-dihydroxy-.kappa.,.kappa.-carotene-6,6'-dione with the best price .
Changzhou Chenqiang Chemical Co., Ltd is a quality supplier of (3S,3'S,5R,5'R)-3,3'-dihydroxy-.kappa.,.kappa.-carotene-6,6'-dione. Our main goal is customer satisfaction. Contact us to negotiate the best price for your business on (3S,3'S,5R,5'R)-3,3'-dihydroxy-.kappa.,.kappa.-carotene-6,6'-dione 470-38-2.
RELATED PRODUCTS