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5-Ethyl-2-nonanol, also known as Ethyl heptanol, is a branched-chain alcohol with a total of nine carbon atoms. It features a heptyl chain (a seven-carbon chain) with an ethyl group attached to the third carbon atom. This organic compound is characterized by its distinct, pleasant, and fruity odor, which is reminiscent of a banana-like scent.

103-08-2

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103-08-2 Usage

Uses

Used in Flavor and Fragrance Industry:
5-Ethyl-2-nonanol is used as a flavoring agent for its characteristic banana-like aroma, adding a fruity note to various food products and beverages.
Used in Perfumery:
In the perfumery industry, 5-Ethyl-2-nonanol is utilized as a fragrance ingredient to provide a fresh and fruity scent to perfumes, colognes, and other scented products.
Used in Cosmetics:
5-Ethyl-2-nonanol is employed in the formulation of cosmetics, where it serves to enhance the sensory experience by imparting a pleasant, fruity smell to products such as lotions, creams, and body care items.
Used in the Food Industry:
As a flavoring agent, 5-Ethyl-2-nonanol is used in the food industry to impart a fruity, banana-like flavor to various food products, enhancing their taste and aroma profile.
Used in the Beverage Industry:
In the beverage industry, 5-Ethyl-2-nonanol is used to add a distinctive fruity note to alcoholic and non-alcoholic beverages, contributing to their overall flavor profile and consumer appeal.

Check Digit Verification of cas no

The CAS Registry Mumber 103-08-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,0 and 3 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 103-08:
(5*1)+(4*0)+(3*3)+(2*0)+(1*8)=22
22 % 10 = 2
So 103-08-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H24O/c1-4-6-7-11(5-2)9-8-10(3)12/h10-12H,4-9H2,1-3H3

103-08-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-ethylnonan-2-ol

1.2 Other means of identification

Product number -
Other names 5-ethyl-nonan-2-ol

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:103-08-2 SDS

103-08-2Downstream Products

103-08-2Relevant academic research and scientific papers

PRO-FRAGRANCE COMPOUNDS

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Page/Page column 21, (2014/12/09)

A compound of Formula (I) wherein R1 represents a C3 to C20 hydrocarbon group derived from a fragrant alcohol of formula R1OH or from a fragrant aryl aldehyde or ketone of Formula (II), wherein: R2 is, independently, hydrogen atom, hydroxyl group, acetoxy group, -O(C=O)CH(CH3), optionally substituted C1-C6 alkyl group or C1-C6 alkoxy group, wherein any two of R2 may form an optionally substituted 5 or 6 membered ring, and R1 represents a radical derived from a fragrant alcohol of formula R1OH or from a fragrant aldehyde or from a fragrant aryl aldehyde or ketone of formula (II). The compounds are useful for example as a precursor for the prolonged delivery or release of fragrant compounds such as fragrant alcohols or aldehydes.

Serine carbonates

-

, (2008/06/13)

Serine carbonates of formula I are precursors for organoleptic compounds, masking agents and antimicrobial agents. Further they are alternative substrates for malodor producing enzymes. The symbols in formula I are defined in claim 1.

Compounds having protected hydroxy groups

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, (2008/06/13)

The present invention relates to compounds with protected hydroxy groups of formula (I) These compounds are precursors for organoleptic agents, such as fragrances, and masking agents and for antimicrobial agents. When activated, the compounds of formula (I) are cleaved and form one or more organoleptic and/or antimicrobial compounds.

Beta-ketoester compounds

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, (2008/06/13)

The beta-ketoesters of formula I are useful as precursors for organoleptic compounds, especially for flavors, fragrances and masking agents and antimicrobial compounds.

Ketone precursors for organoleptic compounds

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, (2008/06/13)

The invention discloses ketones of formula I: wherein, Y is an optionally substituted alkyl, cycloalkyl, or cycloalkylalkyl, wherein each alkyl group is straight or branched and each alkyl and cycloalkyl group is saturated or unsaturated; R1is hydrogen or a C1-6alkyl group that is substituted, saturated or unsaturated, straight or branched; A is a chromophoric substituted aromatic ring or ring system; n is an integer; and with the proviso that formula I is not 2-ethoxy-1-phenyl-ethanone. These compositions are useful for the delivery of organoleptic compounds, especially of flavors, fragrances, masking agents and antimicrobial compounds.

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