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326-61-4

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326-61-4 Usage

Description

PIPERONYL ACETATE is a synthetic flavoring agent characterized by its stable, clear pale yellow liquid form with a heliotrope odor. It is insoluble in water and has a very sweet, light, floral-fruity odor with cherry-like undertones. At low levels, it imparts a sweet, fruity flavor, while at high levels, it becomes bitter. It is typically stored in glass or resin-lined containers.

Uses

Used in Flavor Industry:
PIPERONYL ACETATE is used as a flavoring agent for its floral, soapy, fruity, berry, and slightly jamy taste with a powdery nuance. It is commonly utilized in the flavoring of beverages, candy, ice cream, and baked goods at concentrations of 50–90 ppm.
Used in Food Industry:
In the food industry, PIPERONYL ACETATE is used to add berry notes to various products, enhancing their taste and aroma. Its taste threshold values make it a suitable addition to a range of food items, contributing to their overall flavor profile.
Used in Beverage Industry:
PIPERONYL ACETATE is employed in the beverage industry to provide a unique and pleasant taste to drinks. Its floral, fruity, and berry characteristics make it an ideal choice for flavoring a variety of beverages, from soft drinks to alcoholic drinks.
Used in Cosmetic Industry:
Although not explicitly mentioned in the provided materials, PIPERONYL ACETATE is also known to be used in the cosmetic industry due to its sweet, fruity, and floral odor. It can be used as a fragrance component in various cosmetic products, such as perfumes, lotions, and creams, to provide a pleasant and attractive scent.

Preparation

By acetylation of the corresponding alcohol; by boiling dimethylpiperonyl amine with acetic anhydride.

Air & Water Reactions

Insoluble in water.

Reactivity Profile

PIPERONYL ACETATE is an ester. Esters react with acids to liberate heat along with alcohols and acids. Strong oxidizing acids may cause a vigorous reaction that is sufficiently exothermic to ignite the reaction products. Heat is also generated by the interaction of esters with caustic solutions. Flammable hydrogen is generated by mixing esters with alkali metals and hydrides.

Health Hazard

ACUTE/CHRONIC HAZARDS: PIPERONYL ACETATE is an irritant.

Fire Hazard

PIPERONYL ACETATE is combustible.

Safety Profile

Moderately toxic by ingestion, A skin irritant. When heated to decomposition it emits acrid smoke and irritating fumes.

Check Digit Verification of cas no

The CAS Registry Mumber 326-61-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,2 and 6 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 326-61:
(5*3)+(4*2)+(3*6)+(2*6)+(1*1)=54
54 % 10 = 4
So 326-61-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H10O4/c1-7(11)12-5-8-2-3-9-10(4-8)14-6-13-9/h2-4H,5-6H2,1H3

326-61-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-benzodioxol-5-ylmethyl acetate

1.2 Other means of identification

Product number -
Other names PIPERONYL ACETATE

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:326-61-4 SDS

326-61-4Relevant articles and documents

Proton-exchanged montmorillonite-mediated reactions of hetero-benzyl acetates: Application to the synthesis of Zafirlukast

Yang, Lei,Chen, Xuan,Ni, Kaidong,Li, Yuansheng,Wu, Jianhong,Chen, Weilin,Ji, Yin,Feng, Lili,Li, Fei,Chen, Dongyin

supporting information, (2020/06/28)

Proton-exchanged montmorillonite (H-mont) with outstanding surface characteristics can provide abundant acidic sites in the mesopores, and serve as an efficient heterogeneous catalyst for the synthesis of heterocycle-containing diarylmethanes via Friedel-Crafts-like alkylation of (hetero)arenes by heterobenzyl acetates under mild reaction conditions without requiring any additives or an inert atmosphere. Using this strategy, the gram-scale synthesis of indole-containing diarylmethane 13 has been accomplished in good yield for the preparation of Zafirlukast. In addition, H-mont can be applied to the nucleophilic substitution reactions of heterobenzyl acetate 5p with a variety of alcohols and 1,3-dicarbonyl compounds.

Esterification of Tertiary Amides by Alcohols Through C?N Bond Cleavage over CeO2

Toyao, Takashi,Nurnobi Rashed, Md.,Morita, Yoshitsugu,Kamachi, Takashi,Hakim Siddiki,Ali, Md. A.,Touchy,Kon, Kenichi,Maeno, Zen,Yoshizawa, Kazunari,Shimizu, Ken-ichi

, p. 449 - 456 (2018/09/11)

CeO2 has been found to promote ester forming alcoholysis reactions of tertiary amides. The present catalytic system is operationally simple, recyclable, and it does not require additives. The esterification process displays a wide substrate scope (>45 examples; up to 93 % isolated yield). Results of a density functional theory (DFT) study combined with in situ FT-IR observations indicate that the process proceeds through rate limiting addition of a CeO2 lattice oxygen to the carbonyl group of the adsorbed acetamide species with energy barrier of 17.0 kcal/mol. This value matches well with experimental value (17.9 kcal/mol) obtained from analysis of the Arrhenius plot. Further studies by in situ FT-IR and temperature programmed desorption using probe molecules demonstrate that both acidic and basic properties are important, and consequently, CeO2 showed the best performance for the C?N bond cleavage reaction.

Synthesis, characterization and application of poly(N,N'-dibromo- Nethylnaphthyl-2,7-disulfonamide) as an efficient catalyst for the acetylation and deacetylation reactions

Khazaei, Ardeshir,Saednia, Shahnaz,Roshani, Liela,Kazem-Rostami, Masoud,Zare, Abdolkarim

, p. 159 - 167 (2014/05/20)

In this work, a novel polymer namely poly(N,N'-dibromo-N-ethylnaphthyl-2,7- disulfonamide) (PBNS) is synthesized and characterized by studying its IR, 1H NMR, 13C NMR and thermal gravimetric analysis (TGA). This polymer is utilized as a highly efficient, heterogeneous and recyclable N-bromo reagent to catalyze acetylation of various compounds such as alcohols, phenols, thiol and amine with acetic anhydride under solvent-free conditions, and also it worthily catalyzes deacetylation of acetate esters in aqueous media.

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