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3-Ethyl-4-heptanone is an organic compound with the molecular formula C9H18O. It is a colorless liquid with a strong, pungent odor. This ketone is a member of the heptanone family and is characterized by its unique structure, which includes a seven-carbon chain with an ethyl group attached to the third carbon and a carbonyl group on the fourth carbon. 3-Ethyl-4-heptanone is used as a solvent, a flavoring agent in the food and beverage industry, and as a chemical intermediate in the synthesis of various compounds. It is also found in trace amounts in some natural products, such as essential oils. Due to its volatility and potential health effects, it is important to handle 3-ethyl-4-heptanone with care, following proper safety guidelines.

1528-25-2

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1528-25-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1528-25-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,2 and 8 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1528-25:
(6*1)+(5*5)+(4*2)+(3*8)+(2*2)+(1*5)=72
72 % 10 = 2
So 1528-25-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H18O/c1-4-7-9(10)8(5-2)6-3/h8H,4-7H2,1-3H3

1528-25-2SDS

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 3-ethylheptan-4-one

1.2 Other means of identification

Product number -
Other names 4-Heptanone,3-ethyl

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:1528-25-2 SDS

1528-25-2Downstream Products

1528-25-2Relevant academic research and scientific papers

Catalytic synthesis of oxygenate from alcohol

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Page/Page column 4-8, (2008/06/13)

The present invention discloses a method for catalytic synthesis of oxygenate from alcohol. At first, a feeding material comprising at least one alcohol is provided. Next, a copper-containing catalyst is provided and the catalyst further comprises at least one metal element selected from the group consisting of the following: zinc, magnesium, and aluminum elements. Following that, a catalytic reaction of the feeding material over the copper-containing catalyst is carried out to synthesize at least one oxygenate.

Ethyl-branched aldehydes, ketones, and diketones from caimans (Caiman and Paleosuchus; Crocodylia, Reptilia)

Krueckert, Karsten,Flachsbarth, Birte,Schulz, Stefan,Hentschel, Ute,Weldon, Paul J.

, p. 863 - 870 (2008/09/20)

Secretions from the paracloacal glands of alligators (Alligator spp.) and caimans (Caiman spp., Melanosuchus niger, and Paleosuchus spp.) were examined by GC-MS. The secretions of the common caiman (C. crocodilus), the broad-snouted caiman (C. latirostris), the yacare caiman (C. yacare), the dwarf caiman (P. palpebrosus), and the smooth-fronted caiman (P. trigonatus) yielded a new family of 43 aliphatic carbonyl compounds that includes aldehydes, ketones, and β-diketones with an ethyl branch adjacent to the carbonyl group. The identification of these glandular components and the syntheses and stereochemical investigations of selected compounds are described.

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