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j,c-Carotene, also known as prolycopene, is a naturally occurring carotenoid found in high concentrations in tomatoes and tomato-based products. It is an isomer of the more common lycopene, differing in the arrangement of its double bonds. j,c-Carotene exhibits antioxidant properties, which help protect cells from oxidative stress and damage. Research suggests that it may have potential health benefits, such as reducing the risk of certain cancers and cardiovascular diseases. However, more studies are needed to fully understand its effects and potential applications in human health.

550-29-8

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550-29-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 550-29-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,5 and 0 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 550-29:
(5*5)+(4*5)+(3*0)+(2*2)+(1*9)=58
58 % 10 = 8
So 550-29-8 is a valid CAS Registry Number.

550-29-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name renieratene

1.2 Other means of identification

Product number -
Other names φ,χ-Carotin

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:550-29-8 SDS

550-29-8Relevant academic research and scientific papers

PARTIAL SYNTHESIS OF AROMATIC CAROTENOIDS, TEDANIN, AGELAXANTHIN A, TETHYATENE, AND RENIERATENE

Shimada, Akira,Ezaki, Yoichiro,Inanaga, Junji,Katsuki, Tsutomu,Yamaguchi, Masaru

, p. 773 - 774 (2007/10/02)

Aromatic carotenoids, tedanin, agelaxanthin A, and tethyatene were synthesized from O-acetyl-β-citraurin derived from natural zeaxanthin, and tethyatene was further transformed into renieratene as the first example of aromatization of an alicyclic ring in

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