Conditions | Yield |
---|---|
With ethanol; sodium ethanolate; benzene at 100 - 110℃; |
3,3'-di-keto-β-carotene
aluminum isopropoxide
isopropyl alcohol
benzene
zeaxanthin
(2E,4E,6E,8E,10E,12E,14E)-15-(4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl)-4,9,13-trimethylpentadeca-2,4,6,8,10,12,14-heptaenal
zeaxanthin
Conditions | Yield |
---|---|
With potassium hydroxide In isopropyl alcohol at 20℃; for 3h; | 8.5 mg |
zeaxanthin
Conditions | Yield |
---|---|
With TX-100 In water Rate constant; Irradiation; |
4',5'-didehydro-4,5'-retro-β,β-carotene-3,3'-dione
A
zeaxanthin
B
lutein
C
(3R,3'S,6'R)-lutein
Conditions | Yield |
---|---|
With tellurium; sodium tetrahydroborate In carbon disulfide; ethanol at 40℃; for 0.333333h; Title compound not separated from byproducts; | A 24 % Chromat. B 44 % Chromat. C 31 % Chromat. |
With tellurium; sodium tetrahydroborate In carbon disulfide; ethanol at 40℃; for 0.333333h; | A 24 % Chromat. B 44 % Chromat. C 31 % Chromat. |
Conditions | Yield |
---|---|
In benzene Rate constant; pulse radiolysis; |
zeaxanthin
Conditions | Yield |
---|---|
With aluminum isopropoxide; isopropyl alcohol; benzene |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 11 mg / aq. KOH / propan-2-ol / 24 h / 20 °C 2: 8.5 mg / aq. KOH / propan-2-ol / 3 h / 20 °C View Scheme |
4-(1,4-dihydroxy-2,2,6-trimethylcyclohexyl)-3-butyn-2-ol
zeaxanthin
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: 3.5 g / lithium aluminium hydride / tetrahydrofuran / 3 h / Heating 2: 2.21 g / CHCl3 / 18 h / 20 °C 3: 11 mg / aq. KOH / propan-2-ol / 24 h / 20 °C 4: 8.5 mg / aq. KOH / propan-2-ol / 3 h / 20 °C View Scheme | |
Multi-step reaction with 3 steps 1: 3.5 g / lithium aluminium hydride / tetrahydrofuran / 3 h / Heating 2: 2.21 g / CHCl3 / 18 h / 20 °C 3: 8.5 mg / aq. KOH / propan-2-ol / 3 h / 20 °C View Scheme |
4-(4-hydroxy-2,2,6-trimethylcyclohexylidene)-3-buten-2-ol
zeaxanthin
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 2.21 g / CHCl3 / 18 h / 20 °C 2: 11 mg / aq. KOH / propan-2-ol / 24 h / 20 °C 3: 8.5 mg / aq. KOH / propan-2-ol / 3 h / 20 °C View Scheme | |
Multi-step reaction with 2 steps 1: 2.21 g / CHCl3 / 18 h / 20 °C 2: 8.5 mg / aq. KOH / propan-2-ol / 3 h / 20 °C View Scheme |
zeaxanthin
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 11 mg / aq. KOH / propan-2-ol / 24 h / 20 °C 2: 8.5 mg / aq. KOH / propan-2-ol / 3 h / 20 °C View Scheme |
IUPAC Name: (1R)-4-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-18-[(4R)-4-hydroxy-2,6,6-trimethylcyclohexen-1-yl]-3,7,12,16-tetramethyloctadeca-1,3,5,7,9,11,13,15,17-nonaenyl]-3,5,5-trimethylcyclohex-3-en-1-ol
Synonyms of Zeaxanthin (CAS NO.144-68-3): 3R 3'R Zeaxanthin ; (3R,3'R)-beta,beta-Carotene-3,3'-diol
CAS NO: 144-68-3
Molecular Formula: C40H56O2
Molecular Weight: 568.88
Molecular Structure:
EINECS: 205-636-4
H bond acceptors: 2
H bond donors: 2
Freely Rotating Bonds: 12
Polar Surface Area: 18.46 Å2
Index of Refraction: 1.585
Molar Refractivity: 189.11 cm3
Molar Volume: 564.1 cm3
Surface Tension: 41.2 dyne/cm
Density: 1.008 g/cm3
Flash Point: 273.4 °C
Enthalpy of Vaporization: 118.87 kJ/mol
Boiling Point: 711.4 °C at 760 mmHg
Vapour Pressure: 2.19E-23 mmHg at 25°C
Melting Point: 203-205°C
Storage temp: -20°C
Appearance: Yellow Crystalline Solid
Product Categories of Zeaxanthin (CAS NO.144-68-3): Carotenoids;Intermediates & Fine Chemicals;Pharmaceuticals
Zeaxanthin (CAS NO.144-68-3) is used as a food additive, zeaxanthin is a food dye with E number E161h.
F: 3-8-10
Natural occurrence of Zeaxanthin (CAS NO.144-68-3):
Zeaxanthin is one of the most common carotenoid alcohols found in nature. It is the pigment that gives paprika (made from bell peppers), corn, saffron, and many other plants their characteristic color and Zeaxanthin breaks down to form picrocrocin and safranal, which are responsible for the taste and aroma of saffron.
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