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79516-56-6

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79516-56-6 Usage

Description

(3R,3'R,6'R,9'-cis)-b,e-Carotene-3,3'-diol is a carotenoid compound found in various fruits and vegetables, particularly abundant in carrots. It is a form of vitamin A, essential for maintaining healthy vision, skin, and immune function. Additionally, it possesses antioxidant properties, protecting cells from damage caused by free radicals. (3R,3'R,6'R,9'-cis)-b,e-Carotene-3,3'-diol is an important component in human nutrition and offers potential health benefits.

Uses

Used in Nutritional Supplements:
(3R,3'R,6'R,9'-cis)-b,e-Carotene-3,3'-diol is used as a nutritional supplement to support healthy vision, skin, and immune function. Its vitamin A content is crucial for these bodily functions, and supplementation can help ensure adequate intake, especially for those with dietary deficiencies.
Used in Antioxidant Formulations:
As an antioxidant, (3R,3'R,6'R,9'-cis)-b,e-Carotene-3,3'-diol is used in formulations designed to protect cells from oxidative damage caused by free radicals. Its antioxidant properties can contribute to overall cellular health and may play a role in reducing the risk of certain diseases associated with oxidative stress.
Used in Food and Beverage Industry:
(3R,3'R,6'R,9'-cis)-b,e-Carotene-3,3'-diol is used as a natural colorant in the food and beverage industry to provide a vibrant orange hue to products. Its presence in carrots and other fruits and vegetables makes it a suitable and healthy alternative to synthetic colorants.
Used in Cosmetics and Skincare:
In the cosmetics and skincare industry, (3R,3'R,6'R,9'-cis)-b,e-Carotene-3,3'-diol is used for its beneficial effects on skin health. Its antioxidant properties can help protect the skin from environmental damage, and its vitamin A content may contribute to maintaining skin elasticity and reducing the appearance of fine lines and wrinkles.

Check Digit Verification of cas no

The CAS Registry Mumber 79516-56-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,5,1 and 6 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 79516-56:
(7*7)+(6*9)+(5*5)+(4*1)+(3*6)+(2*5)+(1*6)=166
166 % 10 = 6
So 79516-56-6 is a valid CAS Registry Number.

79516-56-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (9'Z,3R,3'R,6'R)-lutein

1.2 Other means of identification

Product number -
Other names 9'-cis-lutein

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:79516-56-6 SDS

79516-56-6Relevant articles and documents

Combination of carotenoids and epi-lutein

-

Page/Page column 18, (2018/01/20)

The invention describes the preparation and use of carotenoid and epi-lutein compositions to treat various ocular diseases.

Total synthesis of (3R,3′R,6′R)-lutein and its stereoisomers

Khachik, Frederick,Chang, An-Ni

experimental part, p. 3875 - 3885 (2009/10/14)

(Chemical Equation Presented) (3R,3′R,6′R)-Lutein (1) is a major dietary carotenoid that is abundant in most fruits and vegetables commonly consumed in the U.S. and that accumulates in the human plasma, major organs, and ocular tissues. Numerous epidemiol

Confirmation of the absolute (3R,3′S,6′R)-configuration of (all-E)-3′-epilutein

Molnar, Peter,Deli, Jozsef,Osz, Erzsebet,Zsila, Ferenc,Simonyi, Miklos,Toth, Gyula

, p. 2159 - 2168 (2007/10/03)

Circular dichroism (CD) spectroscopy was used to distinguish between the isomeric (all-E)-configured 3′-epilutein (2) and 6′-epilutein (8) to establish the absolute configuration of epilutein samples of different (natural and semisynthetic) origin, including samples of 2 obtained from thermally processed sorrel. Thus, the CD data of lutein (1) and epilutein samples (2) were compared. Our results unambiguously confirmed the (3R,3′S,6′R)- configuration of all epilutein samples. Compound 2 was thoroughly characterized, and its 13C-NMR data are published herewith for the first time.

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