Butyl isobutyrate

Available forms:colorless liquid

pd_proNo:421259-8f276bf1-fe18-4d44-b642-e1581572ef09

pd_productuse:

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Detailed introduction

Reliable Quality Butyl isobutyrate 97-87-0 Hot Sale with Chinese Manufacturer

  • Molecular Formula:C8H16O2
  • Molecular Weight:144.214
  • Appearance/Colour:colorless liquid 
  • Vapor Pressure:0.0275mmHg at 25°C 
  • Melting Point:143 - 144oC 
  • Refractive Index:n20/D 1.401(lit.)  
  • Boiling Point:156.3 °C at 760 mmHg 
  • Flash Point:46.7 °C 
  • PSA:26.30000 
  • Density:0.876 g/cm3 
  • LogP:1.98570 

Butyl isobutyrate(Cas 97-87-0) Usage

Preparation

Prepared from the corresponding acid and n-butyl alcohol by esterification in the presence of concentrated H2SO4 with or without solvent (boiling benzene).

Aroma threshold values

Detection: 80 to 170 ppb

Taste threshold values

Taste characteristics at 30 ppm: fruity, sweet, pineapple, apple, cherry, tutti-frutti, banana.

InChI:InChI=1/C8H16O2/c1-4-5-6-8(2,3)7(9)10/h4-6H2,1-3H3,(H,9,10)/p-1

97-87-0 Relevant articles

Free-Radical Dynamics in Original Lipid Bilayers

Winterle, J. S.,Mill, T.

, p. 6336 - 6338 (1980)

-

Zr-MOF-808 as Catalyst for Amide Esterification

Villoria-del-álamo, Beatriz,Rojas-Buzo, Sergio,García-García, Pilar,Corma, Avelino

supporting information, p. 4588 - 4598 (2020/12/25)

In this work, zirconium-based metal–orga...

PH-Responsive Pickering emulsion stabilized by polymer-coated silica nanoaggregates and applied to recyclable interfacial catalysis

Dong, Jinfeng,Luo, Ruidong,Luo, Yunbai

, p. 42423 - 42431 (2020/12/09)

We first synthesized a diblock copolymer...

A pH-switched Pickering emulsion catalytic system: High reaction efficiency and facile catalyst recycling

Huang, Jianping,Yang, Hengquan

supporting information, p. 7333 - 7336 (2015/04/27)

A smart Pickering emulsion catalytic sys...

Facile Protocol for Water-Tolerant "Frustrated Lewis Pair"-Catalyzed Hydrogenation

Scott, Daniel J.,Simmons, Trevor R.,Lawrence, Elliot J.,Wildgoose, Gregory G.,Fuchter, Matthew J.,Ashley, Andrew E.

, p. 5540 - 5544 (2015/09/15)

Despite rapid advances in the field of m...

97-87-0 Process route

pyrene
129-00-0

pyrene

phthalic anhydride
85-44-9

phthalic anhydride

xanth-9-one
90-47-1

xanth-9-one

pentadecane
629-62-9

pentadecane

n-docosane
629-97-0

n-docosane

n-hexacosane
630-01-3

n-hexacosane

tetradecane
629-59-4

tetradecane

Hexadecane
544-76-3

Hexadecane

Diethylene glycol monobutyl ether
112-34-5,9004-77-7

Diethylene glycol monobutyl ether

n-butyl isobutyrate
97-87-0

n-butyl isobutyrate

heneicosane
629-94-7

heneicosane

n-tricosane
638-67-5

n-tricosane

tetracosane
646-31-1

tetracosane

n-pentacosane
629-99-2

n-pentacosane

cyclopenta[def]phenanthrene
203-63-4

cyclopenta[def]phenanthrene

1,2-benzenedicarboxylic acid diisooctyl ether

1,2-benzenedicarboxylic acid diisooctyl ether

2,6-di-tert-butyl-4-methyl-phenol
128-37-0

2,6-di-tert-butyl-4-methyl-phenol

Diethyl phthalate
84-66-2

Diethyl phthalate

Phthalic acid dibutyl ester
84-74-2

Phthalic acid dibutyl ester

4H-Cyclopenta[def]phenanthrene
203-64-5

4H-Cyclopenta[def]phenanthrene

benzyl n-butyl phthalate
85-68-7

benzyl n-butyl phthalate

1,1'-Biphenyl-2,2',6,6'-tetracarboxaldehyde
4371-26-0

1,1'-Biphenyl-2,2',6,6'-tetracarboxaldehyde

4,5-phenanthrene-8,9-dicarbaldehyde
16162-34-8

4,5-phenanthrene-8,9-dicarbaldehyde

1-hexadecylcarboxylic acid
57-10-3

1-hexadecylcarboxylic acid

6-propyltridecane
55045-10-8

6-propyltridecane

Conditions
Conditions Yield
With oxygen; ozone; In water; for 0.25 - 2h;
butyraldehyde
123-72-8

butyraldehyde

isobutyraldehyde
78-84-2

isobutyraldehyde

isobutyl isobutanoate
97-85-8

isobutyl isobutanoate

n-butyl isobutyrate
97-87-0

n-butyl isobutyrate

butyl butyrate
109-21-7

butyl butyrate

isobutyl n-butyrate
539-90-2

isobutyl n-butyrate

Conditions
Conditions Yield
With dihydridotetrakis(triphenylphosphine)ruthenium; Product distribution; Mechanism; Ambient temperature; other aldehydes; other temp.; also inthe presence of solvents;

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    3-(2-chloro-phenyl)-2-methyl-propionic acid butyl ester

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    methyl (E)-2,2-dimethyl-4-phenyl-3-buten-1-oate

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