Bixin: Difference between revisions
Appearance
Content deleted Content added
Melting point |
rm ball and stick model - who says this represents the conformation? |
||
Line 6: | Line 6: | ||
| ImageSize = 300 |
| ImageSize = 300 |
||
| ImageName = Skeletal formula |
| ImageName = Skeletal formula |
||
| ImageFile1 = Cis-bixin-3D-balls-(rotated).png |
|||
| ImageSize1 = 300 |
|||
| ImageName1 = Ball-and-stick model |
|||
| IUPACName = (2''E'',4''E'',6''E'',8''E'',10''E'',12''E'',14''E'',16''Z'',18''E'')-20-Methoxy-4,8,13,17-tetramethyl-20-oxoicosa-2,4,6,8,10,12,14,16,18-nonaenoic acid |
| IUPACName = (2''E'',4''E'',6''E'',8''E'',10''E'',12''E'',14''E'',16''Z'',18''E'')-20-Methoxy-4,8,13,17-tetramethyl-20-oxoicosa-2,4,6,8,10,12,14,16,18-nonaenoic acid |
||
| OtherNames = ''cis''-Bixin; α-Bixin; 9-''cis''-6,6'-Diapo-ψ,ψ-carotenedioic acid, 6-methyl ester |
| OtherNames = ''cis''-Bixin; α-Bixin; 9-''cis''-6,6'-Diapo-ψ,ψ-carotenedioic acid, 6-methyl ester |
Revision as of 16:22, 15 December 2022
Names | |
---|---|
IUPAC name
(2E,4E,6E,8E,10E,12E,14E,16Z,18E)-20-Methoxy-4,8,13,17-tetramethyl-20-oxoicosa-2,4,6,8,10,12,14,16,18-nonaenoic acid
| |
Other names
cis-Bixin; α-Bixin; 9-cis-6,6'-Diapo-ψ,ψ-carotenedioic acid, 6-methyl ester
| |
Identifiers | |
| |
3D model (JSmol)
|
|
ChEBI | |
ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.027.499 |
PubChem CID
|
|
UNII |
|
CompTox Dashboard (EPA)
|
|
| |
| |
Properties | |
C25H30O4 | |
Molar mass | 394.511 g·mol−1 |
Appearance | Orange crystals |
Melting point | 198 °C (cis-isomer) 217 °C (trans-isomer) |
Insoluble | |
Hazards | |
NFPA 704 (fire diamond) | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|
Bixin is an apocarotenoid found in the seeds of the achiote tree (Bixa orellana)[2] from which it derives its name. It is commonly extracted from the seeds to form annatto, a natural food coloring, containing about 5% pigments of which 70-80% are bixin.[3]
Bixin is chemically unstable when isolated and converts via isomerization into trans-bixin (β-bixin), the double-bond isomer.[1]
Bixin is soluble in fats and alcohols but insoluble in water. Upon exposure to alkali, the methyl ester is hydrolyzed to produce the dicarboxylic acid norbixin, a water-soluble derivative.
References
- ^ a b Merck Index, 11th Edition, 1320
- ^ Bouvier, Florence; Dogbo, Odette; Camara, Bilal (2003). "Biosynthesis of the Food and Cosmetic Plant Pigment Bixin (Annatto)". Science. 300 (5628): 2089–2091. doi:10.1126/science.1085162. ISSN 0036-8075. JSTOR 3834418. PMID 12829782. S2CID 560600.
- ^ Executive Summary Bixin Archived July 21, 2011, at the Wayback Machine, National Toxicology Program