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1-(1,3-benzodioxol-5-yl)-2-hydroxy-2-phenylethanone, commonly known as heliotropin, is a chemical compound characterized by its molecular formula C16H14O4. This aromatic compound is recognized for its sweet, floral, and vanilla-like odor, making it a popular choice as a fragrance ingredient in various industries.

36715-46-5

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36715-46-5 Usage

Uses

Used in Cosmetics Industry:
Heliotropin is used as a fragrance ingredient in the cosmetics industry for its pleasant scent, which enhances the overall fragrance of products such as perfumes and personal care items.
Used in Food Industry:
In the food industry, heliotropin is utilized as an additive to impart a sweet, floral, and vanilla-like aroma to various products, contributing to a more appealing sensory experience for consumers.
Used in Pharmaceutical Industry:
Heliotropin is also employed in the pharmaceutical industry, where its aromatic properties are leveraged to improve the scent of certain medications, making them more palatable for patients.
It is crucial to note that heliotropin should be used in regulated quantities to avoid potential health issues, such as skin irritation, that may arise from excessive exposure.

Check Digit Verification of cas no

The CAS Registry Mumber 36715-46-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,7,1 and 5 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 36715-46:
(7*3)+(6*6)+(5*7)+(4*1)+(3*5)+(2*4)+(1*6)=125
125 % 10 = 5
So 36715-46-5 is a valid CAS Registry Number.

36715-46-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(1,3-benzodioxol-5-yl)-2-hydroxy-2-phenylethanone

1.2 Other means of identification

Product number -
Other names -

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

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More Details:36715-46-5 SDS

36715-46-5Relevant academic research and scientific papers

Synthesis of chiral α-diarylacetic esters by stereospecific 1,2-aryl migration promoted by in situ generated acetals from benzoins

Kothapalli, Raveendra Babu,Niddana, Ramana,Balamurugan, Rengarajan

, p. 1278 - 1281 (2014/04/03)

A simple protocol for the synthesis of α-diarylacetic esters from benzoins is described. In situ generated acetal assists rapid 1,2-aryl migration in a stereospecific manner, paving the way to make enantioenriched α-diarylacetic esters from easily accessi

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