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Heptylacetate, also known as heptyl acetate, is an organic compound with the chemical formula C9H18O2. It is an ester derived from heptyl alcohol and acetic acid, featuring a seven-carbon alkyl chain attached to an acetate group. Heptylacetate is a colorless liquid with a fruity, pear-like odor and is commonly used in the fragrance industry to impart a fresh, fruity scent to various products. It is also found in some natural essential oils, such as apple and pear, and can be used as a flavoring agent in food and beverages. Due to its relatively low toxicity and pleasant aroma, heptylacetate is a popular choice for creating a wide range of scents in personal care products, cleaning agents, and air fresheners.

5921-84-6

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5921-84-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5921-84-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,2 and 1 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5921-84:
(6*5)+(5*9)+(4*2)+(3*1)+(2*8)+(1*4)=106
106 % 10 = 6
So 5921-84-6 is a valid CAS Registry Number.

5921-84-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name heptan-4-yl acetate

1.2 Other means of identification

Product number -
Other names 4-HEPTYL ACETATE

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:5921-84-6 SDS

5921-84-6Relevant academic research and scientific papers

New free-radical halogenations of alkanes, catalysed by N-hydroxyphthalimide. Polar and enthalpic effects on the chemo- and regioselectivity

Minisci, Francesco,Porta, Ombretta,Recupero, Francesco,Gambarotti, Cristian,Paganelli, Roberto,Pedulli, Gian Franco,Fontana, Francesca

, p. 1607 - 1609 (2007/10/03)

Reactions of alkanes with different halogenating systems are compared in order to explore the reactivity of phthalimido-N-oxyl radical in hydrogen abstraction; the importance of polar effects is emphasised.

SELECTIVE OXIDATION OF n-ALKANES WITH LEAD TETRAACETATE

Bestre, R. D.,Cole, E. R.,Crank, G.

, p. 3891 - 3892 (2007/10/02)

Alkanes, when treated with lead tetraacetate under thermal or photochemical conditions, undergo a slow but highly selective oxidation to form secondary acetates.

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