3-Methylbutyraldehyde

Available forms:Colorless liquid

pd_proNo:478632-60da749d-0eb5-4188-9502-ce2647e959b3

pd_productuse:

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Detailed introduction

Top quality factory supply 590-86-3 3-Methylbutyraldehyde at low price

  • Molecular Formula:C5H10O
  • Molecular Weight:86.1338
  • Appearance/Colour:Colorless liquid 
  • Vapor Pressure:30 mm Hg ( 20 °C) 
  • Melting Point:-60 °C 
  • Refractive Index:n20/D 1.388(lit.)  
  • Boiling Point:93.515 °C at 760 mmHg 
  • Flash Point:-1.667 °C 
  • PSA:17.07000 
  • Density:0.792 g/cm3 
  • LogP:1.23140 

Isovaleraldehyde(Cas 590-86-3) Usage

Preparation

By oxidation of isoamyl alcohol.

Air & Water Reactions

Highly flammable.

Reactivity Profile

Isovaleraldehyde is an aldehyde. Aldehydes are frequently involved in self-condensation or polymerization reactions. These reactions are exothermic; they are often catalyzed by acid. Aldehydes are readily oxidized to give carboxylic acids. Flammable and/or toxic gases are generated by the combination of aldehydes with azo, diazo compounds, dithiocarbamates, nitrides, and strong reducing agents. Aldehydes can react with air to give first peroxo acids, and ultimately carboxylic acids. These autoxidation reactions are activated by light, catalyzed by salts of transition metals, and are autocatalytic (catalyzed by the products of the reaction). The addition of stabilizers (antioxidants) to shipments of aldehydes retards autoxidation.

Health Hazard

Inhalation causes chest discomfort, nausea, vomiting, and headache. Contact of liquid with eyes or skin causes irritation. Ingestion causes irritation of mouth and stomach.

Definition

ChEBI: A methylbutanal that is butanal substituted by a methyl group at position 3. It occurs as a volatile constituent in olives.

General Description

Colorless liquid with a weak suffocating odor. Floats on water. Produces an irritating vapor.

InChI:InChI=1/C5H10O/c1-5(2)3-4-6/h4-5H,3H2,1-2H3

590-86-3 Relevant articles

Effective oxidation of alcohols with H5IO6 catalyzed by nickel(II) schiff base complexes

Ramakrishna, Dileep,Bhat, Badekai Ramachandra

, p. 516 - 520 (2010)

Nickel(II)-Schiff base-triphenylphosphin...

Effect of CTAB micelle on the oxidation of L-Leucine by N-Bromophthalimide: A kinetic study

Katre, Yokraj,Goyal, Namita,Kumar Singh, Ajaya

, p. 107 - 124 (2011)

The effect of cationic surfactant cetylt...

Mixed anionic-nonionic micelle catalysed oxidation of aliphatic alcohol in aqueous medium

Acharjee, Animesh,Ali, Md. Ansar,Chowdhury, Suman,Rakshit, Atanu,Saha, Bidyut,Singh, Bula

, (2020)

Oxidation of isoamyl alcohol was carried...

Catalytic oxidation of alcohols by nickel(II) Schiff base complexes containing triphenylphosphine in ionic liquid: An attempt towards green oxidation process

Ramakrishna, Dileep,Bhat, Badekai Ramachandra,Karvembu, Ramasamy

, p. 498 - 501 (2010)

A series of square planar nickel(II) com...

-

Fischer,Ertel,Loewenberg

, p. 34 (1931)

-

Effective oxidation of alcohols by Iron(III)-Schiff base-triphenylphosphine complexes

Rani, Sandya,Bhat, Badekai Ramachandra

, p. 6403 - 6405 (2010)

Iron(III)-Schiff base-triphenylphosphine...

Isobutene hydroformylation in catalytic systems based on rhodium compounds and polyelectrolytes

Sharikova,Kolesnichenko,Markova,Slivinskii

, p. 701 - 703 (1999)

The catalytic properties of water-solubl...

Hydroformylation of olefins in the presence of rhodium carbonyl catalysts immobilized on polymeric pyrrolidinopyridines

Terekhova,Kolesnichenko,Alieva,Markova,Trukhmanova,Slivinsky,Plate

, p. 1583 - 1585 (1996)

The hydroformylation of olefins in the p...

Purification and characterization of isoamyl alcohol oxidase ("Mureka"-forming enzyme)

Yamashita, Nobuo,Motoyoshi, Toru,Nishimura, Akira

, p. 1216 - 1222 (1999)

Isoamyl alcohol oxidase (IAAOD) was puri...

Aerobic oxidation of alcohols with ruthenium catalysts in ionic liquids

Wolfson, Adi,Wuyts, Stijn,De Vos, Dirk E.,Vankelecom, Ivo F.J.,Jacobs, Pierre A.

, p. 8107 - 8110 (2002)

The aerobic oxidations of aliphatic and ...

Mechanistic study of [RuCl3(H2O)2OH]- catalyzed oxidation of L-leucine by acidic N-bromophthalimide

Jain, Bhawana,Singh, Ajaya Kumar,Negi, Reena

, p. 1717 - 1728 (2015)

Kinetic studies in homogenous Ru(III) ca...

Kinetic studies of transition metal ion catalyzed oxidation of some fragrance alcohols

Prabhu,Parbat,Tandel

, p. 6669 - 6673 (2014)

The controlled oxidation of the aliphati...

Dual utility of a single diphosphine-ruthenium complex: A precursor for new complexes and, a pre-catalyst for transfer-hydrogenation and Oppenauer oxidation

Mukherjee, Aparajita,Bhattacharya, Samaresh

, p. 15617 - 15631 (2021/05/19)

The diphosphine-ruthenium complex, [Ru(d...

Solvent-free, microwave assisted oxidation of alcohols with 4-hydroxypyridinium chlorochromate functionalized silica gel

AHMADI, Sayed Ali,GHALEHBANDI, Shermineh Sadat,GHAZANFARI, Dadkhoda,SHEIKHHOSSEINI, Enayatollah

, p. 283 - 289 (2020/10/06)

4-Hydroxypyridinium chlorochromate funct...

Selective Oxidation of Alcohols to Carbonyl Compounds over Small Size Colloidal Ru Nanoparticles

Zhao, JingPeng,Hernández, Willinton Y.,Zhou, WenJuan,Yang, Yong,Vovk, Evgeny I.,Capron, Mickael,Ordomsky, Vitaly

, p. 238 - 247 (2019/11/14)

The selective oxidation of alcohols to c...

590-86-3 Process route

i-Amyl alcohol
123-51-3

i-Amyl alcohol

1-Phenylethanol
98-85-1,13323-81-4

1-Phenylethanol

isovaleraldehyde
590-86-3

isovaleraldehyde

Conditions
Conditions Yield
With aluminium triisopentylate; acetophenone;
i-Amyl alcohol
123-51-3

i-Amyl alcohol

aluminium triisopentylate
25016-92-6

aluminium triisopentylate

acetophenone
98-86-2

acetophenone

1-Phenylethanol
98-85-1,13323-81-4

1-Phenylethanol

isovaleraldehyde
590-86-3

isovaleraldehyde

Conditions
Conditions Yield
pentyl alcohol of fermentation;

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