LUTEIN

PRODUCT IDENTIFICATION

CAS NO. 127-40-2

LUTEIN

EINECS NO. 204-840-0
FORMULA C40H56O2
MOL WT. 568.88

H.S. CODE

3212.90.0000

TOXICITY

 

SYNONYMS beta,epsilon-Carotene-3,3'-diol; Vegetable lutein; vegetable luteol;

4',5'-Didehydro-5',6'-dihydro-beta,beta carotene-3,3'-diol; Xanthophyll; Bo-Xan; Lutein; all-trans-Lutein; gamma-Lutein; Other RN: 1407-74-5; 148124-35-0; 25312-96-3; 28368-07-2; 34026-62-5; 34445-91-5

SMILES

C1([C@H](C(=C[C@@H](C1)O)C)\C=C\C(=C\C=C\C(=C\C=C\C= C(\C=C\C=C(\C=C\C=1C(C[C@H](O)CC1C)(C)C)C)C)C)C)(C)C

CLASSIFICATION

Carotenoid, Biochemical Ex Plants

PHYSICAL AND CHEMICAL PROPERTIES

PHYSICAL STATE

orange to red crystalline powder

MELTING POINT 177 - 178 C
BOILING POINT

 

SPECIFIC GRAVITY

 

SOLUBILITY IN WATER insoluble
pH  
VAPOR DENSITY

 

log Pow 14.82 (Octanol-water)
OH RATE 6.84E-10 (cm3/molecule-sec at 25 C Atmospheric)

REFRACTIVE INDEX

 

NFPA RATINGS

 

AUTOIGNITION

 

FLASH POINT

 

STABILITY Stable under ordinary conditions

GENERAL DESCRIPTION & EXTERNAL LINKS

Carotenoids are plant pigments that involve in light harvesting to participate in energy transfer process in photosynthesis. They absorb light in the 400-500 nm region of the visible spectrum and impart coloration of yellow, orange, red, and purple. They are widely distributed in nature including vegetables, fruits, insects, fishes, and birds. Animals are incapable of synthesizing carotenoids, which should be obtained through diet. Chlorophyll is the generic name for green plant pigments which includes the open-chain bile pigments and the large ring compounds. The structure of chlorophyll molecule has four nitrogen-containing pyrrole rings bonded to a central magnesium atom, and the fifth ring containing only carbon atoms, and various long hydrocarbon tails attached to the pyrrole rings. Carotenoids contain sequences of conjugated isoprene units, alternating double and single carbon bonds. They are sometimes terminated by cyclic end-groups (rings) complemented with hydroxylated, oxidized and hydrogenated groups. The conjugated double bonds absorbs light and UV. The more number of double bonds result in the absorbance of red color wavelength. Changes in geometrical configuration about the double bonds result in the existence of many cis- and trans- isomers. Carotenoids are usually located in quantity in the grana of chloroplasts in the form of carotenoprotein complexes which give blue, green, purple, red, or other colors to the outer surfaces in plants, or eggs of crustaceans, such as the lobster and crab. Carotenoids are classified into carotenes (un-oxidized carotenoids, orange pigments) or xanthophylls (yellow pigments) which contains oxygen and are alcohol-soluble. It is known that more than 600 carotenoids are isolated from natural sources.
  • Carotenes
    • alpha-Carotene
    • beta-Carotene
    • gamma-Carotene
    • delta-Carotene
    • Lycopene
    • Neurosporene
    • Phytofluene
    • Phytoene
  • Xanthophylls
    • Astaxanthin
    • Cantaxanthin
    • Cryptoxanthin
    • gamma-Lutein (xanthophyll)
    • Zeaxanthin

Carotene: though carotene is the simplest of a group of natural pigments called carotenoids, it has  an unsaturated and long aliphatic hydrocarbon chain. It is found as a fat-soluble pigment in many higher plants of dark green leafy and yellow vegetables such as carrots, collards, turnips, sweet potatoes, and squash, and in yellow fruits such as apricots, oranges, peaches, and cantaloupes. Carotene is thought to transport light energy for photosynthesis or contribute to reduction reaction. It is important in animal biology as it is are converted to  retinol in the body by an enzyme in the intestinal wall and the liver. Carotene occurs in several  isomeric forms: alpha, beta, gamma, delta, epsilon, and zeta of which the form of beta acts as an antioxidant nutrient  protecting the body from damaging molecules called free radicals and an immune system booster as it is converted to vitamin A (retinol), important in animal biology as the main dietary source. One molecule of beta-carotene splits into two molecules of vitamin A and thus Beta-carotene is called provitamin A. Cryptoxanthin is a yellow carotenoid widely distributed in egg yolk, green grass, yellow corn which can be converted into vitamin A in the body. Cryptoxanthin is the major precursor of vitamin A together with beta-carotene in humans.

Wikipedia Linking:http://en.wikipedia.org/wiki/Lutein

http://chiro.org
....Lutein and Zeaxanthin belong to the zanthophyll family of carotenoids and are the two major components of the macular pigment of the retina. The macula lutea, or "yellow spot" in the retina is responsible for central vision and visual acuity. Lutein and Zeaxanthin are the only carotenoids found in both the macula and lens of the human eye, and have dual functions in both tissues- to act as powerful antioxidants and to filter high-energy blue light. In addition to playing pivotal roles in ocular health, Lutein and Zeaxanthin are important nutrients in the prevention of cardiovascular disease, stroke, and lung cancer....

SALES SPECIFICATION

APPEARANCE

orange to red crystalline powder

PURITY

20.0% min

HEAVY METALS 10ppm max
ARSENIC

3ppm max

LOSS ON DRYING

1.0% max

MICROBIOLOGICAL
ANALYSIS
Total plate count: not more than 1000/g
Yeast and mold: not more than 100/g
E.coli: neagative
Salmonella: neagative

SOLVENT RESIDUAL

50ppm max

TRANSPORTATION
PACKING
 
HAZARD CLASS  
UN NO.  
EXAMPLES OF NATURALLY-OCCURRING CAROTENOIDS

Astacin

 

Astaxanthin
[CAS#: 472-61-7]

Astaxanthin

Bixin
[CAS#: 6983-79-5 (cis-)
39937-23-0 (trans-)]

 

Canthaxanthin
[CAS#: 514-78-3]

Canthaxanthin

Capsanthin
[CAS#: 465-42-9]

 

alpha-Carotene

alpha-Carotene

beta-Carotene
[CAS #: 7235-40-7]

beta-Carotene

gamma-Carotene
[CAS#: 472-93-5]

gamma-Carotene

delta-Carotene

 

epsilon-Carotene

epsilon-Carotene

zeta-Carotene

zeta-Carotene

alpha-Cryptoxanthin

Diatoxanthin

Didehydroastaxanthin

Didehydroastaxanthin

Fucoxanthin

Fucoxanthin

Fucoxanthinol

Lactucaxanthin

Lactucaxanthin

gamma-Lutein
[CAS #: 127-40-2]

gamma-Lutein

Lycopene
[CAS #: 502-65-8]

Lycopene

Neoxanthin

Neoxanthin

Neurosporene

Neurosporene

Norbixin
[
CAS #: 626-76-6 (cis-)
542-40-5 (trans-)]

 

Peridinin

Peridinin

Phytoene

Phytoene

Rhodopin

Rhodopin

Siphonaxanthin

Siphonaxanthin

Spheroidene

Spheroidene

Spheroidenone

Spheroidenone

Spirilloxanthin

Spirilloxanthin

Uriolide

Uriolide

Violaxanthin
[CAS #: 126-29-4]

 

Zeaxanthin

Zeaxanthin