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AMYL-2-METHYLBUTYRATE is a chemical compound known for its clear, colorless liquid form and a distinctive fruity, banana-like aroma. It is naturally found in fruits such as apple, banana, and strawberry, and is also produced synthetically for use in various applications. Recognized for its safety in small amounts, it has been granted the status of Generally Recognized As Safe (GRAS) by the Food and Drug Administration (FDA), making it a popular choice for enhancing the flavor profile of food and beverage products.

68039-26-9

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68039-26-9 Usage

Uses

Used in Food and Beverage Industry:
AMYL-2-METHYLBUTYRATE is used as a flavoring agent to impart a sweet and aromatic banana-like note to various food and beverage products. Its natural occurrence in fruits and synthetic production make it a versatile ingredient for enhancing the sensory experience of consumables.
Used in Flavor Creation:
AMYL-2-METHYLBUTYRATE is used as a key component in creating artificial fruit flavors, particularly those resembling the taste of bananas and apples. This application is crucial for developing flavor profiles in products where natural fruit content may be limited or to provide a consistent flavor across a product line.
Used in Aromatherapy:
While not explicitly mentioned in the provided materials, given its pleasant aroma, AMYL-2-METHYLBUTYRATE could potentially be used in aromatherapy for its fruity scent, contributing to creating a relaxing or uplifting ambiance.
Used in Perfumery:
Similarly, due to its distinctive fruity aroma, AMYL-2-METHYLBUTYRATE could be utilized in the perfumery industry to add depth and a natural scent note to fragrances.

Check Digit Verification of cas no

The CAS Registry Mumber 68039-26-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,0,3 and 9 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 68039-26:
(7*6)+(6*8)+(5*0)+(4*3)+(3*9)+(2*2)+(1*6)=139
139 % 10 = 9
So 68039-26-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H20O2/c1-4-6-7-8-12-10(11)9(3)5-2/h9H,4-8H2,1-3H3

68039-26-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name Amyl-2-Methylbutyrate

1.2 Other means of identification

Product number -
Other names pentyl 2-methylbutanoate

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:68039-26-9 SDS

68039-26-9Downstream Products

68039-26-9Relevant academic research and scientific papers

Convenient enzymatic resolution of (R,S)-2-methylbutyric acid catalyzed by immobilized lipases

Mittersteiner, Mateus,Linshalm, Bruna Luiza,Vieira, Ana Paula Furlan,Brondani, Patrícia Bulegon,Scharf, Dilamara Riva,de Jesus, Paulo Cesar

, p. 106 - 111 (2017/11/14)

The application of several immobilized lipases has been explored in the enantioselective esterification of (R,S)-2-methylbutyric acid, an insect pheromone precursor. With the use of Candida antarctica B, using hexane as solvent, (R)-pentyl 2-methylbutyrat

Nematicidal activity of natural ester compounds and their analogues against pine wood nematode, bursaphelenchus xylophilus

Seo, Seon-Mi,Kim, Junheon,Koh, Sang-Hyun,Ahn, Young-Joon,Park, Il-Kwon

, p. 9103 - 9108 (2015/03/14)

In this study, we evaluated the nematicidal activity of natural ester compounds against the pine wood nematode, Bursaphelenchus xylophilus, to identify candidates for the development of novel, safe nematicides. We also tested the nematicidal activity of synthesized analogues of these ester compounds to determine the structure-activity relationship. Among 28 ester compounds tested, isobutyl 2-methylbutanoate, 3-methylbutyl 2-methylbutanoate, 3-methylbutyl tiglate, 3-methyl-2-butenyl 2- methylbutanoate, and pentyl 2-methylbutanoate showed strong nematicidal activity against the pine wood nematode at a 1 mg/ mL concentration. The other ester compounds showed weak nematicidal activity. The LC50 values of 3-methylbutyl tiglate, isobutyl 2-methylbutanoate, 3-methylbutyl 2-methylbutanoate, 3-methyl-2-butenyl 2-methylbutanoate, and pentyl 2- methylbutanoate were 0.0218, 0.0284, 0.0326, 0.0402, and 0.0480 mg/mL, respectively. The ester compounds described herein merit further study as potential nematicides for pine wood nematode control.

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