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Y,Y-Carotene, also known as (7-cis,7'-cis,9-cis,9'-cis)-β-carotene, is a naturally occurring isomer of β-carotene, a carotenoid pigment found in various fruits, vegetables, and algae. This specific isomer is characterized by the presence of four cis double bonds, which give it distinct chemical and physical properties compared to the more common all-trans isomer. Y,Y-Carotene plays a crucial role in the human diet as a provitamin A carotenoid, meaning it can be converted into vitamin A (retinol) in the body. It also exhibits antioxidant properties, protecting cells from oxidative stress and potentially reducing the risk of certain diseases. Additionally, it contributes to the vibrant colors of many fruits and vegetables, making it an essential component in the natural pigmentation of these foods.

2361-24-2

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2361-24-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2361-24-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,6 and 1 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2361-24:
(6*2)+(5*3)+(4*6)+(3*1)+(2*2)+(1*4)=62
62 % 10 = 2
So 2361-24-2 is a valid CAS Registry Number.

2361-24-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name ψ,ψ-carotene, 5,6,9,10,13,14,14',13',10',9',6',5'-hexa-cis(?)-lycopene

1.2 Other means of identification

Product number -
Other names ψ,ψ-Carotin, 5,6,9,10,13,14,14',13',10',9',6',5'-Hexa-cis(?)-lycopin

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:2361-24-2 SDS

2361-24-2Relevant academic research and scientific papers

Synthesis, Isolation, and NMR-Spectroscopic Characterization of Fourteen (Z)-Isomers of Lycopene and of Some Acetylenic Didehydro- and Tetradehydrolycopenes

Hengartner, Urs,Bernhard, Kurt,Meyer, Karl,Englert, Gerhard,Glinz, Ernst

, p. 1848 - 1865 (2007/10/02)

Eight (Z)-isomers of lycopene were prepared by stereocontrolled syntheses and fully characterized by 1H-NMR, 13C-NMR, mass, and UV/VIS-spectroscopy: (5Z)-, (7Z)-, (15Z)-, (5Z,5'Z)-, (7Z,7'Z)-, (7Z,9Z)-, (9Z,9'Z)-, and (7Z,9Z,7'Z,9'Z)-lycopene.Six additional (Z)-isomers, namely (9Z)-, (13Z)-, (5Z,9'Z)-, (9Z,13'Z)-, (5Z,9Z,5'Z)-, and (5Z,13Z,5'Z)-lycopene, were isolated in small quantities from isomer mixtures by semiprep.HPLC and were identified by 1H-NMR spectroscopy.

Synthesen von Carotinen mit ψ-Endgruppen und (Z)-Konfiguration an terminalen konjugierten Doppelbindungen

Zumbrunn, Albrecht,Uebelhart, Peter,Eugster, Conrad Hans

, p. 1519 - 1539 (2007/10/02)

Five carotenes bearing (5Z)-ψ-end groups were synthesized and carefully characterized: (5Z)-lycopene (6), (5Z,5'Z)-lycopene (7), (5'Z)-neurosporene (8), (5'Z)-β,ψ-carotene (12), and (5'Z)-εψ-carotene (14).

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