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3-methyl-3-butenyl 3-methyl-2-butenoate is a chemical compound with the molecular formula C9H14O2. It is an ester, consisting of a 3-methyl-3-butenyl group bonded to a 3-methyl-2-butenoate group.
Used in Fragrance Industry:
3-methyl-3-butenyl 3-methyl-2-butenoate is used as a fragrance ingredient for its fruity and floral odor, resembling that of peach and apple.
Used in Flavor Industry:
3-methyl-3-butenyl 3-methyl-2-butenoate is used as a flavoring agent in the production of beverages, confectionery, and baked goods.
Used in Organic Synthesis:
3-methyl-3-butenyl 3-methyl-2-butenoate is used as a precursor in organic synthesis for the preparation of various other compounds.

72928-35-9

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72928-35-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72928-35-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,9,2 and 8 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 72928-35:
(7*7)+(6*2)+(5*9)+(4*2)+(3*8)+(2*3)+(1*5)=149
149 % 10 = 9
So 72928-35-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H16O2/c1-8(2)5-6-12-10(11)7-9(3)4/h7H,1,5-6H2,2-4H3

72928-35-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methylbut-3-enyl 3-methylbut-2-enoate

1.2 Other means of identification

Product number -
Other names 3-methyl-3-buten-1-yl 3-methyl-2-butenoate

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:72928-35-9 SDS

72928-35-9Downstream Products

72928-35-9Relevant academic research and scientific papers

Analysis of the volatile aroma constituents of parental and hybrid clones of pepino (Solanum muricatum)

Rodriguez-Burruezo, Adrian,Kollmannsberger, Hubert,Prohens, Jaime,Nitz, Siegfried,Nuez, Fernando

, p. 5663 - 5669 (2004)

The volatile constituents of 10 clones (4 parents with different flavors and 6 hybrids from selected crossings among these parents) of pepino fruit (Solanum muricatum) were isolated by simultaneous distillation-extraction and analyzed by gas chromatography-mass spectrometry (GC-MS). Odor-contributing volatiles (OCVs) were detected by GC-olfactometry-MS analyses and included 24 esters (acetates, 3-methylbutanoates, and 3-methylbut-2-enoates), 7 aldehydes (especially hexenals and nonenals), 6 ketones, 9 alcohols, 3 lactones, 2 terpenes, β-damascenone, and mesifurane. Among these compounds, 17, of which 5 had not been reported previously in pepino, were found to contribute significantly to pepino aroma. OCVs can be assigned to three groups according to their odor quality: fruity fresh (acetates and prenol), green vegetable (C6 and C9 aidehydes), and exotic (lactones, mesifuran, and β-damascenone). Quantitative and qualitative differences between clones for these compounds are clearly related to differences in their overall flavor impression. The positive value found for the hybrid-midparent regression coefficient for volatile composition indicates that an important fraction of the variation observed is inheritable, which has important implications in breeding for improving aroma. Significant and positive correlations were found between OCVs having common precursors or related pathways.

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