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Furfuryl isobutyrate is a colorless liquid chemical compound with the formula C9H10O3, derived from furfuryl alcohol and isobutyric acid. It possesses a fruity odor and is commonly used in various industries due to its distinct properties.

6270-55-9

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6270-55-9 Usage

Uses

Used in Food and Beverage Industry:
Furfuryl isobutyrate is used as a flavoring agent for its fruity odor, enhancing the taste and aroma of various food and drink products.
Used in Perfume and Fragrance Industry:
Furfuryl isobutyrate is utilized as a component in perfumes and fragrances, contributing to the creation of pleasant and long-lasting scents.

Check Digit Verification of cas no

The CAS Registry Mumber 6270-55-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,7 and 0 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6270-55:
(6*6)+(5*2)+(4*7)+(3*0)+(2*5)+(1*5)=89
89 % 10 = 9
So 6270-55-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H12O3/c1-7(2)9(10)12-6-8-4-3-5-11-8/h3-5,7H,6H2,1-2H3

6270-55-9SDS

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 isobutyric acid furfuryl ester

1.2 Other means of identification

Product number -
Other names Propanoic acid, 2-methyl-, 2-furanylmethyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Food additives -> Flavoring Agents
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:6270-55-9 SDS

6270-55-9Downstream Products

6270-55-9Relevant academic research and scientific papers

Stereoisomeric effects in thermo-remendable polymer networks based on diels-alder crosslink reactions

Canadell, Judit,Fischer, Hartmut,De With, Gijsbertus,Van Benthem, Rolf A. T. M.

body text, p. 3456 - 3467 (2011/05/02)

This study describes the synthesis, the spectroscopic, and the thermal characterization of linear and crosslinked polymers as well as a number of corresponding model compounds, containing Diels-Alder adducts derived from furan and maleimide groups. The thermal reversibility (rDA, DA) of structurally varied model compounds, polymeric and network structures were studied by differential scanning calorimetry, where possible in combination with 1H NMR spectroscopy. It was established that the endo and exo DA stereoisomers show significantly different thermal responses: the rDA of the endo DA-adducts typically takes place at 20-40 K lower temperatures than that of the corresponding exo DA-adducts in all cases, with the exception of some aromatic maleimides. Although In situ isomerization was observed to a limited extent and only In some cases, this effect is not expected to influence the thermoremendability of DA-crosslinked networks being dependent on two separate stereoisomeric rDA steps.

REVERSIBLE POLYMERIC GELATION FOR OILFIELD APPLICATIONS

-

, (2009/05/28)

This invention relates to the synthesis and use in oilfield applications of copolymers which can undergo the Diels-Alder reaction to form a gel. Under appropriate conditions, the retro Diels-Alder reaction can take place to provide for decreasing the viscosity of the aforementioned gel.

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