Methylbutyl ethanoate

Synonyms Acetic acid, isopentyl ester Acetic acid, 3-methylbutyl ester AI3-00576 Banana oil BRN 1744750 CCRIS 6051 EINECS 204-662-3 FEMA No. 2055 Isoamyl ethanoate Isopentyl acetate Isopentyl alcohol acetate 3-Methyl-1-butanol acetate 3-Methylbutyl acetate 3-Methyl-1-butyl acetate 3-Methylbutyl ethanoate NSC 9260 Pear oil UN 1104. 

Methylbutyl acetate, see sec-Amyl acetate 3-Methylbutyl acetate, see Isoamyl acetate 3-Methyl-l-butyl acetate, see Isoamyl acetate 3-Methylbutyl ethanoate, see Isoamyl acetate Methylbutyl ethyl ketone, see 5-Methyl-3-heptanone Methyl n-butyl ketone, see 2-Hexanone Methylcarbamate-l-naphthalenol, see Carbaryl Methylcarbamate-l -naphthol, see Carbaryl Methyl carbamic acid, 2,3-dihydro-2,2-dimethyl-7-... 

When ethanoic acid and 3-methylbutanol undergo a condensation reaction, the ester 3-methylbutyl ethanoate is formed. The water molecule eliminated is made up of the -OH group from the acid and the H- from the alcohol. 

Esters are mildly polar and have pleasant aromas. Many esters are found in natural foodstuffs banana oil (3-methylbutyl ethanoate common name, isoamyl acetate), pineapples (ethyl butanoate common name, ethyl butyrate), and raspberries (isobutyl methanoate common name, isobutyl formate) are but a few... 

METHYLBUTYL ETHANOATE (123-92-2) Forms explosive mixture with air (flash point 77°F/25°C). Reacts violently with strong oxidizers. Incompatible with strong alkalis, strong acids, nitrates. Attacks asbestos softens and dissolves many plastics, rubber, and coatings. 

SYNONYMS banana oil, isoamyl ethanoate, isopentyl acetate, 3-methyl-1-butanol acetate, 3-methylbutyl ester of acetic acid, 3-methylbutyl ethanoate. 

GH3)jGHGH2GH200GGH3, which is a bee alarm pheromone that signals danger to a honey bee. If this compound is warmed with aqueous sodium hydroxide, a slow reaction takes place to produce sodium ethanoate and 3-methylbutan-l-ol. The reaction is first order with respect to both 3-methylbutyl ethanoate and the aqueous hydroxide ion. Explain the term first order and give experimental details showing how this information could be obtained. [8]... 

Methylbutyl ethanoate. See Isoamyl acetate Methyl t-butyl ether... 

Suppose you carried out the following synthesis of 3-methylbutyl ethanoate (isoamyl acetate) ... 

Methylbutyl ethanoate Pentyl ethanoate Propyl butanoate... 

Acetic acid hexyl ester see Hexyl ethanoate 123-92-2 Acetic acid isoamyl ester see 3-Methylbutyl ethanoate 110-19-0 Acetic acid isohutyl ester 2-Methylpropyl ethanoate... 

Isoamyl acetate see 3-Methylbutyl ethanoate Isoamyl alcohol see 3-Methylbutan-l-ol heta.-Isoamylene see 2-Methylbut-2-ene Isohutane see 2-Methylpropane Isohutanoic acid see 2-Methylpropanoic acid Isohutanol see 2-Methylpropan-l-ol Isobutene see 2-Methylpropene Isobutyl acetate see 2-Methylpropyl ethanoate Isobutyl alcohol see 2-Methylpropan-l-ol Isobutylbenzene see (2-Methylpropyl)benzene Isobutyl chloride see l-Chloro-2-methylpropane Isobutylene see 2-Methylpropene Isobutylene oxide see 2,2-Dimethyloxirane Isobutyl ethanoate see 2-Methylpropyl ethanoate Isobutyl methyl ketone see 4-Methylpentan-2-one Isobutyraldehyde see 2-Methylpropanal Isobutyric acid see 2-Methylpropanoic acid Isocyanic acid butyl ester see Butyl isocyanate Isohexane see 2-Methylpentane Isooctane see 2,2,4-Tiimethylpentane Isopentane see 2-Methylbutane Isopentanol see 3-Methylbutan-l-ol Isopentyl alcohol see 3-Methylbutan-l-ol Isoprene see 2-Methylbuta-l,3-diene Isopropanol see Propan-2-ol Isopropenylbenzene... 

The odors of esters are distinctly different from those of the corresponding acids. Acids have unpleasant smells, but esters have fruity smells. In fact, esters are responsible for the odors of many fruits. For example, ethyl ethanoate occurs in pineapples, 3-methylbutyl ethanoate in apples and bananas, 3-methylbutyl-3-methylbutanoate in apples, and octyl ethanoate in oranges. 

C5H10O2 + C6H12O2 + C7H14O2 + Isopropyl ethanoate + 2-Methylpropyl ethanoate + 3-Methylbutyl ethanoate EVLM 1231 EVLM 1231 EVLM 1231 LB2638 LB0245 LB0855... 

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