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16698-35-4

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  • High Content Natural Extract [2R[2R*(4R*,8R*)]]-3,4-dihydro-2,5,8-trimethyl-2-(4,8,12-trimethyltridecyl)-2H-benzopyran-6-ol HACCP manufacturer

    Cas No: 16698-35-4

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16698-35-4 Usage

Description

[2R[2R(4R,8R)]]-3,4-dihydro-2,5,8-trimethyl-2-(4,8,12-trimethyltridecyl)-2H-benzopyran-6-ol is a naturally occurring form of Vitamin E, characterized by its brownish-yellow oil appearance. It is biologically less active than α-Tocopherol, which is the most active form of Vitamin E.

Uses

Used in Pharmaceutical Industry:
[2R[2R(4R,8R)]]-3,4-dihydro-2,5,8-trimethyl-2-(4,8,12-trimethyltridecyl)-2H-benzopyran-6-ol is used as a pharmaceutical ingredient for its antioxidant properties. It helps protect cells from oxidative damage and supports overall health.
Used in Cosmetic Industry:
In the cosmetic industry, [2R[2R(4R,8R)]]-3,4-dihydro-2,5,8-trimethyl-2-(4,8,12-trimethyltridecyl)-2H-benzopyran-6-ol is used as an antioxidant in skincare products. It helps to protect the skin from environmental stressors and supports skin health.
Used in Food Industry:
[2R[2R(4R,8R)]]-3,4-dihydro-2,5,8-trimethyl-2-(4,8,12-trimethyltridecyl)-2H-benzopyran-6-ol is used as a natural antioxidant in the food industry. It helps to extend the shelf life of food products and maintain their freshness.
Used in Nutraceutical Industry:
In the nutraceutical industry, [2R[2R(4R,8R)]]-3,4-dihydro-2,5,8-trimethyl-2-(4,8,12-trimethyltridecyl)-2H-benzopyran-6-ol is used as a dietary supplement for its antioxidant and health-promoting properties. It supports overall well-being and helps to maintain a healthy immune system.

Check Digit Verification of cas no

The CAS Registry Mumber 16698-35-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,6,9 and 8 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 16698-35:
(7*1)+(6*6)+(5*6)+(4*9)+(3*8)+(2*3)+(1*5)=144
144 % 10 = 4
So 16698-35-4 is a valid CAS Registry Number.
InChI:InChI=1/C28H48O2/c1-20(2)11-8-12-21(3)13-9-14-22(4)15-10-17-28(7)18-16-25-24(6)26(29)19-23(5)27(25)30-28/h19-22,29H,8-18H2,1-7H3

16698-35-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name TOCOPHEROL, D-β-(P)

1.2 Other means of identification

Product number -
Other names -

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:16698-35-4 SDS

16698-35-4Relevant articles and documents

Kinetics of the reaction by which natural vitamin E is regenerated by vitamin C

Nagaoka, Shin-ichi,Kakiuchi, Takuhiro,Ohara, Keishi,Mukai, Kazuo

, p. 26 - 32 (2007)

The rate constant and activation energy of the regeneration reaction of natural vitamin E by vitamin C were determined with a double-mixing stopped-flow spectrophotometer. The formation of vitamin C radical was observed in the absorption spectrum. The kinetic effect of methyl substitution on the aromatic ring of vitamin E radical indicates that partial charge-transfer plays a role in the reaction. Since a substantial deuterium kinetic isotope effect was not found, the tunneling effect may not play an important role under the present experimental conditions.

Process of separating chiral isomers of chroman compounds and their derivatives and precursors

-

Page/Page column 15, (2012/12/13)

The present invention relates to a process of separating chiral isomers of chroman compounds, particularly tocopherols and tocotrienols as well as the esters and intermediates thereof. It has been found that this process allows a separation of the desired isomer with a higher yield and enables the use of the non-desired isomers in a very efficient way. Said process is particularly useful when implemented in an industrial process. Furthermore, it has been found that this process allows using isomer mixtures as they result from traditional industrial synthesis.

Tocopherols by hydride reduction of dialkylamino derivatives

Netscher, Thomas,Mazzini, Francesco,Jestin, Roselyne

, p. 1176 - 1183 (2008/02/08)

Aminomethylation with Mannich reagents derived from secondary amines and paraformaldehyde under improved conditions has been used to convert non-α-tocopherol homologues into α-tocopherol, the biologically most important vitamin E compound. Mono- and bis(aminomethylated) β-, γ-and δ-tocopherol were then subsequently transformed into the corresponding tocopherols (α- and β-tocopherol) by reductive deamination. As an alternative to classical catalytic hydrogenation in the last step, efficient laboratory protocols using complex hydrides have been derived and applied to the preparation of labelled vitamin E compounds. Wiley-VCH Verlag GmbH & Co. KGaA, 2007.

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