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52046-71-6

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52046-71-6 Usage

Description

1-(4-hydroxyphenyl)-3-phenylpropane-1,3-dione, commonly known as curcumin, is a naturally occurring chemical compound derived from the spice turmeric. It is characterized by its bright yellow color and is renowned for its potential health benefits, which include anti-inflammatory and antioxidant properties. Curcumin has been a staple in traditional medicine for many years and is currently under investigation for its possible therapeutic applications in various health conditions.

Uses

Used in Food Industry:
Curcumin is utilized as a natural coloring and flavoring agent in the food industry due to its vibrant yellow hue and unique taste.
Used in Traditional Medicine:
Curcumin has been employed in traditional medicine for centuries, leveraging its anti-inflammatory and antioxidant properties to address a range of health issues.
Used in Pharmaceutical Applications:
Curcumin is being explored for its potential in treating various health conditions such as arthritis, cancer, and neurodegenerative diseases, given its demonstrated anti-inflammatory and antioxidant effects.
Used as a Natural Alternative to Anti-inflammatory Medications:
Curcumin is also being investigated as a possible natural alternative to conventional anti-inflammatory and pain-relief medications, offering a potentially safer and more natural option for patients.

Check Digit Verification of cas no

The CAS Registry Mumber 52046-71-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,0,4 and 6 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 52046-71:
(7*5)+(6*2)+(5*0)+(4*4)+(3*6)+(2*7)+(1*1)=96
96 % 10 = 6
So 52046-71-6 is a valid CAS Registry Number.

52046-71-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-hydroxyphenyl)-3-phenylpropane-1,3-dione

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:52046-71-6 SDS

52046-71-6Relevant articles and documents

Europium(III) β-diketone complex as portable luminescent chemosensor for naked eye Cu2+ detection and recyclable on-off-on vapor response

Cao, Fangyi,Yuan, Zheng,Liu, Junhua,Ling, Jun

, p. 102535 - 102541 (2015)

A novel Eu3+ complex coordinated by polymers with β-diketone pendant groups (Eu3+-PDKMA) has been synthesized for Cu2+ cation and acid-base vapor detections. Its sensitive and selective response to Cu2+ is confi

Influence of substituent on UV absorption and keto-enol tautomerism equilibrium of dibenzoylmethane derivatives

Zawadiak, Jan,Mrzyczek, Marek

supporting information, p. 815 - 819 (2012/11/13)

UV absorption spectra of dibenzoylmethane and its 23 derivatives with acetamide, tert-butyl, chloride, fluoride, hydroxyl, methyl, methoxy and nitro substituents in aromatic rings were collected. General influence of substituent on absorption maxima and absorption intensity was defined. Hyperchromic effects were observed for diketones with electron-donating groups in para postion. The keto-enol tautomerism equilibrium constant of obtained compounds was investigated with 1H NMR spectroscopy. Significant changes of equilibrium were observed only for ortho substituted compounds. Results revealed dissimilarity of substituent effects on absorption and keto-enol tautomerism of aromatic β-diketones.

Sunblocking polymers and their novel formulations

-

, (2008/06/13)

Novel polymeric biologically inert compositions and their intermediates, as well as sunscreen formulations comprising them and making them invisible, are provided for broad range protection from ultraviolet radiation. Acryl polymers comprising at least two different ultraviolet absorbing moieties having different light absorbing ranges are employed in conjunction with other monomers to provide sunscreen polymers as microparticles. The polymer microparticles, once imbibed with carrier compounds, change the refractive index, thus providing invisible sunscreen formulations which offer enhanced protection without adverse physiological effects.

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