ChemicalBook > CAS DataBase List > Isovaleraldehyde

Isovaleraldehyde

Product Name
Isovaleraldehyde
CAS No.
590-86-3
Chemical Name
Isovaleraldehyde
Synonyms
3-METHYLBUTANAL;3-METHYLBUTYRALDEHYDE;Isovaleral;Butanal,3-methyl-;3-Methyl-1-butanal;3-Methylbutan-1-al;ISOVALERIC ALDEHYDE;3-Methybutanol;Isovaleraldehyde,98%;methylbutanal,3-methylbutanal
CBNumber
CB0351221
Molecular Formula
C5H10O
Formula Weight
86.13
MOL File
590-86-3.mol
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Isovaleraldehyde Property

Melting point:
-60 °C
Boiling point:
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)
refractive index 
n20/D 1.388(lit.)
FEMA 
2692 | 3-METHYLBUTYRALDEHYDE
Flash point:
29 °F
storage temp. 
2-8°C
solubility 
alcohol: miscible, soluble in Propylene glycol and oils.
form 
Liquid
Specific Gravity
0.80
color 
Clear colorless to light yellow
Odor
at 0.10 % in dipropylene glycol. ethereal aldehydic chocolate peach fatty
Odor Type
aldehydic
Odor Threshold
0.0001ppm
explosive limit
1.7-6.8%(V)
Water Solubility 
15 g/L (20 ºC)
Merck 
14,5229
JECFA Number
258
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.
InChIKey
YGHRJJRRZDOVPD-UHFFFAOYSA-N
LogP
1.5 at 25℃ and pH7
CAS DataBase Reference
590-86-3(CAS DataBase Reference)
NIST Chemistry Reference
Butanal, 3-methyl-(590-86-3)
EPA Substance Registry System
Isovaleraldehyde (590-86-3)
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Safety

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
Autoignition Temperature
464 °F
TSCA 
Yes
HazardClass 
3
PackingGroup 
II
HS Code 
29121900
Hazardous Substances Data
590-86-3(Hazardous Substances Data)
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H225Highly Flammable liquid and vapour

H317May cause an allergic skin reaction

H319Causes serious eye irritation

H335May cause respiratory irritation

H411Toxic to aquatic life with long lasting effects

Precautionary statements

P210Keep away from heat/sparks/open flames/hot surfaces. — No smoking.

P273Avoid release to the environment.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
W269212
Product name
Isovaleraldehyde
Purity
natural, ≥95%, FG
Packaging
100g
Price
$190
Updated
2024/03/01
Sigma-Aldrich
Product number
W269212
Product name
Isovaleraldehyde
Purity
natural, ≥95%, FG
Packaging
1kg
Price
$914
Updated
2024/03/01
Sigma-Aldrich
Product number
W269204
Product name
Isovaleraldehyde
Purity
≥97%, FG
Packaging
1kg
Price
$146
Updated
2024/03/01
Sigma-Aldrich
Product number
W269204
Product name
Isovaleraldehyde
Purity
≥97%, FG
Packaging
4kg
Price
$326
Updated
2024/03/01
Sigma-Aldrich
Product number
W269204
Product name
Isovaleraldehyde
Purity
≥97%, FG
Packaging
20kg
Price
$1020
Updated
2024/03/01
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Isovaleraldehyde Chemical Properties,Usage,Production

Chemical Properties

3-Methylbutyraldehyde has a choking, powerful, acrid, pungent, apple-like odor. This compound is also reported to have a fruity, fatty, animal, almond odor.

Chemical Properties

Isovaleraldehyde is a colorless, low-solubility liquid with a pungent odor similar to that of apples.

Occurrence

Reported found in over 180 natural sources including apple, banana, berries, grapes, peach, papaya, peach, kohlrabi, carrot, celery, leek, peas, potato, bell pepper, tomato, ginger, peppermint and spearmint oil, other Mentha oils, vinegar, breads, many cheeses, butter, milk, egg, fatty and lean fish, meats, hop oil, beer, cognac, sherry, rum, grape wines, cocoa, coffee, tea, filberts, peanuts, pecans, peanut butter, barley, oats, soybean, honey, avocado, mace, plum, beans, mushrooms, starfruit, mango, beetroot, cardamom, coriander seed, rice, lovage leaf, pumpkin, buckwheat, laurel, malt, clary sage, wort, elderberry, clam, scallops, crab, crayfish, okra, sapodilla, truffles, kiwifruit and other sources.

Uses

Isovaleraldehyde is manufactured by oxidizing isoamyl alcohol with sodium perchromate and sulfuric acid. Isovaleraldehyde is present in essential oils of orange, peppermint, lemon, and other plants and fruits. Its main uses are as an artificial flavor additive and in perfumes.

Uses

Isovaleraldehyde acts as a reagent in the preparation of active pharmaceutical ingredient (API) products. It serves as an internal standard for the determination of wine aroma carbonyl compounds with 5-8 carbon atoms. Further, it is utilized as a standard to evaluate the quality of olive oils by headspace solid-phase microextraction-gas chromatography using flame ionization detection and multivariate analysis. In addition to this, it is employed to enhance the taste and odor of the food.

Uses

In artificial flavors and perfumes.

Definition

ChEBI: 3-methylbutanal is a methylbutanal that is butanal substituted by a methyl group at position 3. It occurs as a volatile constituent in olives. It has a role as a flavouring agent, a plant metabolite, a volatile oil component and a Saccharomyces cerevisiae metabolite.

Preparation

By oxidation of isoamyl alcohol.

General Description

Colorless liquid with a weak suffocating odor. Floats on water. Produces an irritating vapor. It is a metabolite found in or produced by Saccharomyces cerevisiae.

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

Raw materials

Dichromic acid 3-Methyl-1-butanol

Preparation Products

6-ISO-PROPYL-3H-THIENO[2,3-D]PYRIMIDIN-4-ONE 6-Methyl-3-hepten-2-one 5-Methyl-2-isopropyl-2-hexenal 2-AMINO-5-ISOPROPYL-THIOPHENE-3-CARBOXYLIC ACID ETHYL ESTER octamylamine 3-Methylbutyl 3-methylbutanoate Isovaleric acid 4-METHYL-1-PHENYL-2-PENTANOL
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View Lastest Price from Isovaleraldehyde manufacturers

Baoji Guokang Bio-Technology Co., Ltd.
Product
Isovaleraldehyde 590-86-3
Price
US $56.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
2000T
Release date
2021-06-02
Hebei Yanxi Chemical Co., Ltd.
Product
Isovaleraldehyde 590-86-3
Price
US $40.00/kg
Min. Order
1kg
Purity
0.99
Supply Ability
10 tons
Release date
2023-10-17
Hebei Weibang Biotechnology Co., Ltd
Product
Isovaleraldehyde 590-86-3
Price
US $0.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
100 MT
Release date
2024-10-25

590-86-3, IsovaleraldehydeRelated Search:

Sodium carboxymethyl cellulose Methyl methacrylate Methacrylic acid N,N-Dimethylformamide Valeraldehyde Methyl cellulose POLY(VINYL BUTYRAL) Dimethyl sulfoxide Isovaleryl chloride ISOVALERIC ANHYDRIDE 2-Methylbutane 3-Methyl-2-buten-1-ol 3-Methyl-1-butanethiol Isovaleric acid Ethyl isovalerate 2-Hexenamide, 2-cyano-5-methyl- Hexanoic acid,3-(aminomethyl)-5-methyl-, (3R)- 2,4-Dicyano-3-(2-Methylpropyl)-pentanediaMide

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  • eraL
  • 3-METHYLBUTANAL
  • 3-METHYLBUTYRALDEHYDE
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  • Natural 3-Methybutanol
  • 3-Methybutanol
  • Natural Isoamyl Aldehyde
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