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The chemical in question is a long-chain fatty acid known as 2,4,6,8,10,12,14,16,18-Nonadecanonaenoic acid, which is characterized by its 19 carbon atoms and multiple double bonds in a specific pattern (2E,4E,6E,8E,10E,12E,14E,16E,18E). 2,4,6,8,10,12,14,16,18-Nonadecanonaenoic acid, 4,8,13,17-tetramethyl-19-(2,6,6-trimethyl-1-cyclohexen-1-yl)-, (2E,4E,6E,8E,10E,12E,14E,16E,18E)- is also described as 4,8,13,17-tetramethyl-19-(2,6,6-trimethyl-1-cyclohexen-1-yl)-, indicating the presence of four methyl groups at the 4th, 8th, 13th, and 17th carbon positions, and a cyclohexenyl group at the 19th position with specific methyl substitutions. This complex structure suggests that the compound has a high degree of unsaturation and a unique branched and cyclic structure, which could influence its physical properties and potential applications in various fields such as biochemistry, pharmaceuticals, or materials science.

6900-46-5

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6900-46-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6900-46-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,0 and 0 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6900-46:
(6*6)+(5*9)+(4*0)+(3*0)+(2*4)+(1*6)=95
95 % 10 = 5
So 6900-46-5 is a valid CAS Registry Number.

6900-46-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 6'-apo-β-caroten-6'-oic acid

1.2 Other means of identification

Product number -
Other names (2E,4E,6E,8E,10E,12E,14E,16E,18E)-4,8,13,17-Tetramethyl-19-(2,6,6-trimethyl-cyclohex-1-enyl)-nonadeca-2,4,6,8,10,12,14,16,18-nonaenoic acid

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:6900-46-5 SDS

6900-46-5Downstream Products

6900-46-5Relevant academic research and scientific papers

Light harvesting and photoprotective functions of carotenoids in compact artificial photosynthetic antenna designs

Kodis, Gerdenis,Herrero, Christian,Palacios, Rodrigo,Marinì?o-Ochoa, Ernesto,Gould, Stephanie,De La Garza, Linda,Van Grondelle, Rienk,Gust, Devens,Moore, Thomas A.,Moore, Ana L.,Kennis, John T.M.

, p. 414 - 425 (2004)

Artificial light-harvesting constructs were synthesized by covalently linking two carotenoids to the central silicon atom of a phthalocyanine (Pc) derivative. Triad 1 binds two carotenoids having nine conjugated double bonds, whereas triad 2 binds two carotenoids having 10 carbon-carbon double bonds in conjugation. Fluorescence excitation experiments indicated that, in triad 1 dissolved in n-hexane, the carotenoid to Pc singlet energy transfer efficiency is ca. 92%, whereas in triad 2, it is 30%. Results from ultrafast laser spectroscopy indicate that upon population of the optically allowed S2 state of the carotenoid the optically forbidden states S1 and S* are rapidly generated in both triad 1 and triad 2. In triad 1, S2, S1 and S* all contribute singlet electronic energy to Pc. In triad 2, singlet electronic energy transfer to Pc occurs primarily from the optically allowed S2 state with little energy transfer to Pc via the S1 state, and there is no evidence for energy transfer via S*. Instead, in triad 2, we find a multiphased quenching of the Pc singlet excited state on the picosecond and nanosecond time scales. Upon intersystem crossing from the singlet excited state of Pc to the triplet state in triad 1, triplet-triplet energy transfer to either of the carotenoids takes place on a time scale significantly shorter than 5 ns. When dissolved in polar solvents, triads 1 and 2 exhibit light-induced electron transfer from either of the carotenoid moieties to the excited singlet Pc species with a time constant of about 2 ps. Charge recombination to the singlet ground state occurs in 10 ps in triad 1 and 17 ps in triad 2.

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