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106950-13-4

6-Ethyl-4-methoxy-2-pyranone, commonly known as ethyl maltol, is a chemical compound characterized by its sweet, fruity aroma and flavor. It is derived from maltol, a naturally occurring compound found in plants such as pine needles and roasted malt. Ethyl maltol is known for its ability to enhance the flavor and aroma of various food products, particularly in confectionery and bakery items. Moreover, it possesses antioxidant properties and has been studied for its potential health benefits, making it a versatile and widely-used chemical compound in the food and fragrance industries.

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  • 106950-13-4 Structure

  • Basic information

    1. Product Name: 6-ETHYL-4-METHOXY-2-PYRANONE
    2. Synonyms: 6-ETHYL-4-METHOXY-2-PYRANONE;6-Ethyl-4-Methoxy-pyran-2-one;6-Ethyl-4-Methoxy-2H-pyran-2-one
    3. CAS NO:106950-13-4
    4. Molecular Formula: C8H10O3
    5. Molecular Weight: 154.17
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 106950-13-4.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 291.506 °C at 760 mmHg
    3. Flash Point: 117.878 °C
    4. Appearance: /
    5. Density: 1.114 g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: Sealed in dry,Room Temperature
    8. Solubility: N/A
    9. CAS DataBase Reference: 6-ETHYL-4-METHOXY-2-PYRANONE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-ETHYL-4-METHOXY-2-PYRANONE(106950-13-4)
    11. EPA Substance Registry System: 6-ETHYL-4-METHOXY-2-PYRANONE(106950-13-4)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 106950-13-4(Hazardous Substances Data)

106950-13-4 Usage

Uses

Used in Food and Beverage Industry:
6-Ethyl-4-methoxy-2-pyranone is used as a flavoring agent for its sweet, fruity aroma and flavor, enhancing the taste and aroma of various food products, especially in confectionery and bakery items.
Used in Fragrance Industry:
Ethyl maltol is utilized in the fragrance industry for its pleasant aroma, contributing to the creation of various scent compositions.
Used in Antioxidant Applications:
Due to its antioxidant properties, 6-Ethyl-4-methoxy-2-pyranone has potential health benefits and is studied for its possible use in antioxidant formulations to support overall health and well-being.

Check Digit Verification of cas no

The CAS Registry Mumber 106950-13-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,9,5 and 0 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 106950-13:
(8*1)+(7*0)+(6*6)+(5*9)+(4*5)+(3*0)+(2*1)+(1*3)=114
114 % 10 = 4
So 106950-13-4 is a valid CAS Registry Number.

106950-13-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-Ethyl-4-methoxy-2-pyranone

1.2 Other means of identification

Product number -
Other names 6-ethyl-4-methoxypyran-2-one

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:106950-13-4 SDS

106950-13-4Relevant articles and documents

SERINE HYDROLASE INHIBITORS

-

Page/Page column 71-73, (2008/06/13)

Provided herein are benzoxazinone compounds of formula (I) and compositions containing the compounds. The compounds and compositions are useful in the methods of inhibiting the action of serine hydrolase, including neutrophil elastase. In certain embodiments, the compounds and compositions are useful in the prevention, amelioration or treatment of serine hydrolase-mediated diseases.

Synthesis of austrocorticinic acid

Deshpande,Khan,Ayyanagar

, p. 790 - 793 (2007/10/03)

The total synthesis of austrocorticinic acid 2 is described from methyl orsellinate dimethyl ether 4 and 6-ethyl-4-methoxy-2-pyrone 5.

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