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Isovaleraldehyde Basic information

Product Name:	Isovaleraldehyde
Synonyms:	3-METHYLBUTANAL;3-METHYLBUTYRALDEHYDE;ISOAMYLALDEHYDE;ISOVALERIC ALDEHYDE;ISOVALERALDEHYDE;ISOPENTALDEHYDE;ISO-PENTANAL;FEMA 2692
CAS:	590-86-3
MF:	C5H10O
MW:	86.13
EINECS:	209-691-5
Product Categories:
Mol File:	590-86-3.mol

Isovaleraldehyde Chemical Properties

mp	-60 °C
bp	90 °C(lit.)
density	0.803 g/mL at 25 °C(lit.)
vapor density	2.96 (vs air)
vapor pressure	30 mm Hg ( 20 °C)
FEMA	2692
refractive index	n20/D 1.388(lit.)
Fp	29 °F
storage temp.	Refrigerator (+4°C) + Flammables area
Water Solubility	15 g/L (20 ºC)
Merck	14,5229
BRN	773692
Stability:	Stable, but light and air sensitive. Highly flammable. Readily forms explosive mixtures with air. Incompatible with strong oxidizing agents, bases, reducing agents, air.
CAS DataBase Reference	590-86-3(CAS DataBase Reference)
NIST Chemistry Reference	Butanal, 3-methyl-(590-86-3)
EPA Substance Registry System	Butanal, 3-methyl-(590-86-3)

Safety Information

Hazard Codes	F,Xi
Risk Statements	11-36-36/37/38-43-36/37
Safety Statements	7-16-26-36-37/39-37-24-9
RIDADR	UN 1989 3/PG 2
WGK Germany	1
RTECS	ES3450000
F	13
HazardClass	3
PackingGroup	II
HS Code	29121900
Hazardous Substances Data	590-86-3(Hazardous Substances Data)

MSDS Information

Provider	Language
Isovaleraldehyde	English
SigmaAldrich	English
ACROS	English
ALFA	English

Isovaleraldehyde Usage And Synthesis

Chemical Properties	colourless liquid with a strong and (for some
General Description	Colorless liquid with a weak suffocating odor. Floats on water. Produces an irritating vapor.
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.

Isovaleraldehyde Preparation Products And Raw materials

Preparation Products	Isovaleric acid-->3-Methylbutyl 3-methylbutanoate-->6-ISO-PROPYL-3H-THIENO[2,3-D]PYRIMIDIN-4-ONE-->2-AMINO-5-ISOPROPYL-THIOPHENE-3-CARBOXYLIC ACID ETHYL ESTER-->octamylamine-->4-METHYL-1-PHENYL-2-PENTANOL-->6-Methyl-3-hepten-2-one-->5-Methyl-2-isopropyl-2-hexenal
Raw materials	3-Methyl-1-butanol

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