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3-Decyldihydro-2(3H)-furanone, also known as 3-decyltetrahydro-2H-pyran-2-one, is a chemical compound characterized by its faint, sweet, and creamy odor. It is synthesized in laboratories and occurs naturally in certain plants, fruits, and seafood, where it contributes to the distinctive aroma of some types of cheese. 3-DECYLDIHYDRO-2(3H)-FURANONE is considered safe for consumption in small quantities and has been approved for use in various consumer products by regulatory agencies.

2983-19-9

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2983-19-9 Usage

Uses

Used in Food Industry:
3-Decyldihydro-2(3H)-furanone is used as a flavoring agent in food products for its ability to impart a sweet and creamy aroma, enhancing the overall sensory experience of the food items.
Used in Personal Care and Household Products Industry:
In the personal care and household products industry, 3-decyldihydro-2(3H)-furanone is used as a fragrance ingredient to provide a pleasant and subtle scent to products such as perfumes, soaps, and detergents.
Used in Aroma Compounds:
3-Decyldihydro-2(3H)-furanone is used as an important aroma component in the production of cheese, where it contributes to the unique and desirable flavor profile of certain types of cheese.

Check Digit Verification of cas no

The CAS Registry Mumber 2983-19-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,8 and 3 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2983-19:
(6*2)+(5*9)+(4*8)+(3*3)+(2*1)+(1*9)=109
109 % 10 = 9
So 2983-19-9 is a valid CAS Registry Number.
InChI:InChI=1/C14H26O2/c1-2-3-4-5-6-7-8-9-10-13-11-12-16-14(13)15/h13H,2-12H2,1H3

2983-19-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-decyloxolan-2-one

1.2 Other means of identification

Product number -
Other names 3-Decyl-dihydro-furan-2-on

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:2983-19-9 SDS

2983-19-9Downstream Products

2983-19-9Relevant academic research and scientific papers

Radical reaction by a combination of phosphinic acid and a base in aqueous media

Yorimitsu,Shinokubo,Oshima

, p. 225 - 235 (2007/10/03)

Treatment of various organic halides with phosphinic acid (hypophosphorous acid) in aqueous ethanol in the presence of a radical initiator and a base gave the corresponding reduced products in high yields. Addition of a base is indispensable for the reduction of halides by phosphinic acid. Allylic ether of o-iodophenol or 2-haloalkanal allylic acetal underwent radical cyclization under the same conditions to afford the corresponding cyclic product in excellent yield. Deuterated phosphinic acid was found to be an efficient chain carrier for the radical deuteration of organic halides. For example, a deuterium oxide solution of deuterated phosphinic acid, potassium carbonate, 2,2′-azobis(isobutyramidine) dihydrochloride as an initiator, and p-iodobenzoic acid was heated at reflux to give p-deuteriobenzoic acid in 94% yield. A mixed dioxane/D2O solvent system combined with DBU and potassium peroxodisulfate was crucial to deuterate hydrophobic substrates in high yields and with high deuterium incorporation. Complete deuterium incorporation was accomplished only by the reaction in D2O without an organic cosolvent and an organic base.

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