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542-40-5

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542-40-5 Usage

Description

NORBIXIN(P), also known as Norbixin, is a natural carotenoid derived from the plant Tagetes erecta. It is a pigment that is widely used in the food and cosmetic industries due to its vibrant color and natural origin. NORBIXIN(P) is characterized by its golden yellow hue and is known for its stability and safety in various applications.

Uses

Used in Food Industry:
NORBIXIN(P) is used as a food coloring agent for imparting a golden yellow color to products such as butter and cheese. Its natural origin and vibrant color make it a popular choice for enhancing the appearance of these dairy products.
Used in Cosmetic Industry:
NORBIXIN(P) is also used as a pigment in the cosmetic industry, where it is valued for its ability to provide a rich, golden yellow color to various products. Its natural and stable properties make it a preferred choice for use in the formulation of cosmetics, ensuring a visually appealing and safe product for consumers.

Check Digit Verification of cas no

The CAS Registry Mumber 542-40-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,4 and 2 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 542-40:
(5*5)+(4*4)+(3*2)+(2*4)+(1*0)=55
55 % 10 = 5
So 542-40-5 is a valid CAS Registry Number.

542-40-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (2E,4E,6E,8E,10E,12E,14E,16E,18E)-4,8,13,17-tetramethylicosa-2,4,6,8,10,12,14,16,18-nonaenedioic acid

1.2 Other means of identification

Product number -
Other names E 160b

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Food Additives: COLOUR
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:542-40-5 SDS

542-40-5Upstream product

542-40-5Downstream Products

542-40-5Relevant articles and documents

Hydrophilic carotenoids: Surface properties and aggregation behavior of the potassium salt of the highly unsaturated diacid norbixin

Breukers, Stefanie,pstad, Christer L.,Sliwka, Hans-Richard,Partali, Vassilia

, p. 1741 - 1747 (2009)

The oft-claimed 'good' water solubility of the food color norbixin (3) could not be confirmed. In contrast, the potassium salt 5 of norbixin formed suitable dispersions. The surface and aggregation properties of salt 5 were investigated and compared with

NOVEL INTERMEDIATES FOR PREPARING NORBIXIN OR BIXIN ETHYL ESTER AND METHODS THEREOF

-

Paragraph 0146; 0148-0152, (2020/10/13)

The present invention relates to a method for preparing a carotenoid compound, norbixin or bixin ethyl ester, from a novel intermediate compound. When using the novel intermediate compound, norbixin or bixin ethyl ester can be prepared in high yield through a simple process.

Thermal degradation kinetics of bixin in an aqueous model system

Rios, Alessandro De O.,Borsarelli, Claudio D.,Mercadante, Adriana Z.

, p. 2307 - 2311 (2007/10/03)

The kinetics of the thermal degradation of the natural cis carotenoid bixin in a water/ethanol (8:2) solution was studied as a function of temperature (70-125°C), using high-performance liquid chromatography. The curves for the decay of bixin and formation of products (e.g., di-cis and all-trans isomers and a C17 degradation compound) did not adjust well to a first-order rate law, but very good fits were obtained using a biexponential model. This mathematical modeling gave the rate constant values for the formation of the primary products from bixin, and the energy barrier for each step was obtained. The di-cis isomers were formed immediately (15 kcal/mol) together with the decay of bixin, followed by a slow consumption, indicating their role as reaction intermediates. In fact, the di-cis isomers could easily revert to bixin (Ea ≈ 3 kcal/mol) or yield the primary C17 degradation product, with an energy barrier of 6.5 kcal/mol. In turn, 24 kcal/mol was necessary for the Bix - all-trans step, explaining its slower formation.

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