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432-70-2

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432-70-2 Usage

Description

.beta.,.epsilon.-Carotene, also known as cyclic carotene, is a type of carotenoid found in various plants and is characterized by the presence of a beta-ring and an epsilon-ring at opposite ends. It plays a crucial role in the synthesis of vitamin A and contributes to the vibrant colors of many fruits and vegetables.

Uses

Used in Nutritional Supplements:
.beta.,.epsilon.-Carotene is used as a nutritional supplement for its provitamin A activity, which helps in the synthesis of vitamin A in the human body. This is particularly important for maintaining good vision, a healthy immune system, and overall growth and development.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, .beta.,.epsilon.-Carotene is used as an ingredient in the development of medications targeting various health conditions. Its antioxidant properties make it a valuable component in the formulation of drugs aimed at reducing the risk of chronic diseases.
Used in Food Industry:
.beta.,.epsilon.-Carotene is used as a natural colorant in the food industry, adding vibrant hues to products such as juices, snacks, and other processed foods. Its natural origin and health benefits make it a preferred choice over synthetic colorants.
Used in Cosmetics Industry:
In the cosmetics industry, .beta.,.epsilon.-Carotene is utilized for its antioxidant and anti-aging properties. It is often included in skincare products, such as creams and serums, to help protect the skin from environmental damage and promote a youthful appearance.
Used in Cancer Prevention:

Biochem/physiol Actions

One of the primary isomers of carotene, racemic form of metabolite in carotenoid biosynthesis, biosynthesis of plant secondary metabolites, biosynthesis of terpenoids and steroids and the biosynthesis of secondary metabolites

Check Digit Verification of cas no

The CAS Registry Mumber 432-70-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,3 and 2 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 432-70:
(5*4)+(4*3)+(3*2)+(2*7)+(1*0)=52
52 % 10 = 2
So 432-70-2 is a valid CAS Registry Number.

432-70-2SDS

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 α-carotene

1.2 Other means of identification

Product number -
Other names alpha-carotene

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:432-70-2 SDS

432-70-2Downstream Products

432-70-2Relevant articles and documents

Kinetic Model for Studying the Isomerization of α- and β-Carotene during Heating and Illumination

Chen, B. H.,Chen, T. M.,Chien, J. T.

, p. 2391 - 2397 (2007/10/02)

The thermoisomerization and iodine-catalyzed photoisomerization of all-trans-α- and all-trans-β-carotene were kinetically studied using regression models. Carotene samples were heated at varied temperatures or exposed to a 20 W light for varied lengths of time. Isomerization and degradation reactions were monitored using HPLC with diode array detection. Four cis isomers of β-carotene and three cis isomers of α-carotene were separated and detected. The degradations of both carotenes under heating at 150 deg C or iodine/light treatment may fit the reversible first- order model. 9-cis and 13-cis were the major β-carotene isomers formed during heating, while 13,15-di-cis was favored during iodine-catalyzed photoisomerization. The formation of 9-cis and 13-cis form all-trans-α-carotene was dependent upon the extent of heat or iodine/light treatment, and the latter was formed in greater amount under either treatment. Keywords: α-Carotene; β-carotene; thermoisomerization; photoisomerization; kinetic study

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