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1,3-Pentanedione, 4,4,5,5,5-pentafluoro-1-phenylis a chemical compound that is primarily known for its use as a flavoring agent in the food industry. It imparts a buttery or creamy taste to various food products, enhancing their flavor profile. However, there are concerns regarding its potential health risks, as it has been identified as a respiratory irritant and a possible hazard for respiratory sensitization. Studies have also suggested a link between exposure to 1,3-Pentanedione, 4,4,5,5,5-pentafluoro-1-phenyl- and the development of bronchiolitis obliterans, a severe lung disease. Due to these concerns, there have been calls for further investigation and regulation of its use in food and consumer products.

1799-50-4

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1799-50-4 Usage

Uses

Used in Food Industry:
1,3-Pentanedione, 4,4,5,5,5-pentafluoro-1-phenylis used as a flavoring agent for its ability to impart a buttery or creamy taste to various food products. This enhances the overall flavor profile and consumer appeal of these products.
However, due to the potential health risks associated with 1,3-Pentanedione, 4,4,5,5,5-pentafluoro-1-phenyl-, there is a need for further investigation and regulation of its use in the food industry. The concerns include its classification as a respiratory irritant and a potential hazard for respiratory sensitization, as well as the suggested link to the development of bronchiolitis obliterans, a serious lung disease. As a result, it is crucial to evaluate the safety and potential alternatives to ensure the well-being of consumers.

Check Digit Verification of cas no

The CAS Registry Mumber 1799-50-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,9 and 9 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1799-50:
(6*1)+(5*7)+(4*9)+(3*9)+(2*5)+(1*0)=114
114 % 10 = 4
So 1799-50-4 is a valid CAS Registry Number.

1799-50-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,4,5,5,5-pentafluoro-1-phenylpentane-1,3-dione

1.2 Other means of identification

Product number -
Other names 1,3-Pentanedione,4,4,5,5,5-pentafluoro-1-phenyl

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:1799-50-4 SDS

1799-50-4Relevant academic research and scientific papers

α-Pentafluoropropionylation of Ketones and Aldehydes Using Hexafluoropropene Oxide. A Facile Synthesis of Fluorinated 1,3-Diketones

Ishihara, Takashi,Seki, Toshio,Ando, Teiichi

, p. 3345 - 3346 (1982)

Hexafluoropropene oxide reacts smoothly with morpholine enamines from ketones and aldehydes at 0 deg C to room temperature in anhydrous THF to give pentafluorinated 1,3-diketones in good yields.The keto-enol equilibrium in the products is generally in favor of their enol form.

Regioselective synthesis of 4-alkyl- and 4-aryl-6-(perfluoroalkyl)salicylic acid derivatives by formal [3+3] cyclocondensation of 1,3-bis(silyloxy)-1,3-butadienes with 3-silyloxy-1-(perfluoroalkyl)prop-2-en-1-ones

Büttner, Stefan,Lubbe, Mathias,Reinke, Helmut,Fischer, Christine,Langer, Peter

, p. 7968 - 7976 (2008/12/20)

4-Alkyl- and 4-aryl-6-(perfluoroalkyl)salicylic acid derivatives were regioselectively prepared by [3+3] cyclization of 1,3-bis(silyl enol ethers) with 3-silyloxy-1-(perfluoroalkyl)prop-2-en-1-ones.

Modulators of LXR

-

, (2008/06/13)

Compounds, compositions and methods for modulating the activity of nuclear receptors are provided. In particular, heterocyclic compounds are provided for modulating the activity of nuclear receptors, including liver X receptor (LXR) and orphan nuclear receptors. In certain embodiments, the compounds are N-substituted pyridones.

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