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Isovaleric acid

CAS No.
503-74-2
Chemical Name:
Isovaleric acid
Synonyms
3-METHYLBUTANOIC ACID;3-METHYLBUTYRIC ACID;ISOPENTANOIC ACID;isopentanoic;3-methylbutyrate;Isovalerianic acid;3-Methybutyric Acid;Butanoicacid,3-methyl-;FEMA 3102;Aroma Name
CBNumber:
CB8729604
Molecular Formula:
C5H10O2
Molecular Weight:
102.13
MDL Number:
MFCD00002726
MOL File:
503-74-2.mol
MSDS File:
SDS
Last updated:2023-11-28 16:31:44

Isovaleric acid Properties

Melting point -29 °C (lit.)
Boiling point 175-177 °C (lit.)
Density 0.925 g/mL at 20 °C (lit.)
vapor pressure 0.38 mm Hg ( 20 °C)
refractive index n20/D 1.403(lit.)
FEMA 3102 | ISOVALERIC ACID
Flash point 159 °F
storage temp. Store below +30°C.
solubility 48g/l
form Liquid
pka 4.77(at 25℃)
color Clear colorless to slightly yellow
Specific Gravity 0.928 (20/20℃)
PH 3.92(1 mM solution);3.4(10 mM solution);2.89(100 mM solution);
Odor at 1.00 % in propylene glycol. sour stinky feet sweaty cheese tropical
Odor Type cheesy
explosive limit 1.5-6.8%(V)
Water Solubility 25 g/L (20 ºC)
Merck 14,5231
JECFA Number 259
BRN 1098522
Dielectric constant 2.6(20℃)
LogP 1.7 at 25℃
Substances Added to Food (formerly EAFUS) ISOVALERIC ACID
FDA 21 CFR 172.515
CAS DataBase Reference 503-74-2(CAS DataBase Reference)
EWG's Food Scores 1
FDA UNII 1BR7X184L5
NIST Chemistry Reference Butanoic acid, 3-methyl-(503-74-2)
EPA Substance Registry System Isovaleric acid (503-74-2)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS05
Signal word  Danger
Hazard statements  H314
Precautionary statements  P280-P301+P330+P331-P303+P361+P353-P304+P340+P310-P305+P351+P338-P363
Hazard Codes  C,T
Risk Statements  34-24-22
Safety Statements  26-36/37/39-45-38-28A
RIDADR  UN 3265 8/PG 2
WGK Germany  1
RTECS  NY1400000
13
Autoignition Temperature 824 °F
TSCA  Yes
HS Code  2915 60 90
HazardClass  6.1
PackingGroup  III
Toxicity LD50 i.v. in mice: 1120±30 mg/kg (Or, Wretlind)
NFPA 704
2
3 0

Isovaleric acid price More Price(31)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich W310212 Isovaleric Acid natural, ≥98%, FG 503-74-2 1kg $191 2024-03-01 Buy
Sigma-Aldrich W310212 Isovaleric Acid natural, ≥98%, FG 503-74-2 5kg $683 2024-03-01 Buy
Sigma-Aldrich 129542 Isovaleric acid 99% 503-74-2 100ml $33.4 2024-03-01 Buy
Sigma-Aldrich 129542 Isovaleric acid 99% 503-74-2 500ml $69.7 2024-03-01 Buy
Sigma-Aldrich W310212 Isovaleric Acid natural, ≥98%, FG 503-74-2 100g $74.9 2023-01-07 Buy
Product number Packaging Price Buy
W310212 1kg $191 Buy
W310212 5kg $683 Buy
129542 100ml $33.4 Buy
129542 500ml $69.7 Buy
W310212 100g $74.9 Buy

Isovaleric acid Chemical Properties,Uses,Production

Description

Isovaleric acid has a characteristic disagreeable odor. It is extremely penetrating and persistent with a sour taste. May be synthesized by oxidation of isoamyl alcohol or isovaleric aldehyde.

Chemical Properties

Isovaleric acid has a characteristic disagreeable, rancid, cheese-like odor. It is extremely penetrating and persistent with a sour taste. May consist of one or a mixture of isomers or n-pentanoic acid and/or 2- or 3-methyl butanoic acid. Consumption: Annual: 1850.00 lb

Chemical Properties

clear colorless to slightly yellow liquid

Occurrence

Of the three possible isomers of n-valeric acid, only isovaleric acid has extensive application in flavoring; originally reported in seal and dolphin fat; subsequently isolated from valerian. Also reported found in the essential oils of cypress, citronella, laurel leaves, cajeput, Cymbopogon javanensis, hops, Persea pubescens, geranium, American peppermint, spearmint, rosemary, lemongrass, Eucalyptus goniocalyx and other spp., tobacco, Monarda fistulos, Thymus mastichina, Artemisia frigida, and probably in lavender; reported among the constituents of petitgrain lemon. Also reported found in many foods including apple, currants, guava, grapes, papaya, peach, pineapple, raspberry, strawberry, potato, bell pepper, vinegar, breads, many cheeses, fish, chicken, lamb, hop oil, beer, cognac, whiskies, cider, sherry, grape wines, rum, cocoa, tea, coffee, honey, soybean, passion fruit, mushrooms, marjoram, plum, brandy, starfruit, trassi, rice, jackfruit, sake, sukiyaki, buckwheat, corn oil, cashew apple, malt, wort, Bourbon vanilla, shrimp, mussels, cherimoya, Cape gooseberry and Chinese quince frui

Uses

Isovaleric acid is used extensively as a flavoring ingredient in nonalcoholic beverages and in foods such as ice cream, candy, baked goods, and cheese, as a fragrance ingredient in perfumes, and as a chemical intermediate in the manufacture of sedatives and other pharmaceutical products. It is also used as an extractant of mercaptans from petroleum hydrocarbons, a vinyl stabilizer, and as an intermediate in the manufacture of plasticizers and synthetic lubricants.

Uses

A molecular entity capable of donating a hydron to an acceptor (Bronsted base). It is a favorable carbon source for cell growth. Moreover, it is a promising odor indicator.

Uses

In flavors, perfumes, manufacture of sedatives.

Definition

ChEBI: A C5, branched-chain saturated fatty acid.

Preparation

By oxidation of isoamyl alcohol or isovaleric aldehyde

Aroma threshold values

Detection: 190 ppb to 2.8 ppm

Synthesis Reference(s)

Chemical and Pharmaceutical Bulletin, 30, p. 2787, 1982 DOI: 10.1248/cpb.30.2787
Tetrahedron Letters, 23, p. 3135, 1982 DOI: 10.1016/S0040-4039(00)88578-0

General Description

Isovaleric acid is a colorless liquid with a penetrating odor. Isovaleric acid is slightly soluble in water. Isovaleric acid is corrosive to metals and to tissue.

Air & Water Reactions

Isovaleric acid is slightly soluble in water.

Reactivity Profile

Isovaleric acid is a carboxylic acid. Carboxylic acids donate hydrogen ions if a base is present to accept them. They react in this way with all bases, both organic (for example, the amines) and inorganic. Their reactions with bases, called "neutralizations", are accompanied by the evolution of substantial amounts of heat. Neutralization between an acid and a base produces water plus a salt. Carboxylic acids with six or fewer carbon atoms are freely or moderately soluble in water; those with more than six carbons are slightly soluble in water. Soluble carboxylic acid dissociate to an extent in water to yield hydrogen ions. The pH of solutions of carboxylic acids is therefore less than 7.0. Many insoluble carboxylic acids react rapidly with aqueous solutions containing a chemical base and dissolve as the neutralization generates a soluble salt. Carboxylic acids in aqueous solution and liquid or molten carboxylic acids can react with active metals to form gaseous hydrogen and a metal salt. Such reactions occur in principle for solid carboxylic acids as well, but are slow if the solid acid remains dry. Even "insoluble" carboxylic acids may absorb enough water from the air and dissolve sufficiently in Isovaleric acid to corrode or dissolve iron, steel, and aluminum parts and containers. Carboxylic acids, like other acids, react with cyanide salts to generate gaseous hydrogen cyanide. The reaction is slower for dry, solid carboxylic acids. Insoluble carboxylic acids react with solutions of cyanides to cause the release of gaseous hydrogen cyanide. Flammable and/or toxic gases and heat are generated by the reaction of carboxylic acids with diazo compounds, dithiocarbamates, isocyanates, mercaptans, nitrides, and sulfides. Carboxylic acids, especially in aqueous solution, also react with sulfites, nitrites, thiosulfates (to give H2S and SO3), dithionites (SO2), to generate flammable and/or toxic gases and heat. Their reaction with carbonates and bicarbonates generates a harmless gas (carbon dioxide) but still heat. Like other organic compounds, carboxylic acids can be oxidized by strong oxidizing agents and reduced by strong reducing agents. These reactions generate heat. A wide variety of products is possible. Like other acids, carboxylic acids may initiate polymerization reactions; like other acids, they often catalyze (increase the rate of) chemical reactions.

Hazard

Strong irritant to tissue.

Health Hazard

TOXIC; inhalation, ingestion or skin contact with material may cause severe injury or death. Contact with molten substance may cause severe burns to skin and eyes. Avoid any skin contact. Effects of contact or inhalation may be delayed. Fire may produce irritating, corrosive and/or toxic gases. Runoff from fire control or dilution water may be corrosive and/or toxic and cause pollution.

Fire Hazard

Non-combustible, substance itself does not burn but may decompose upon heating to produce corrosive and/or toxic fumes. Some are oxidizers and may ignite combustibles (wood, paper, oil, clothing, etc.). Contact with metals may evolve flammable hydrogen gas. Containers may explode when heated.

590-86-3
503-74-2
Synthesis of Isovaleric acid from Isovaleraldehyde
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View Lastest Price from Isovaleric acid manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Isovaleric acid pictures 2024-04-19 Isovaleric acid
503-74-2
US $3310.00-3000.00 / Tons 1Tons 99.99% 200Tons Hebei Dangtong Import and export Co LTD
isovaleric acid pictures 2023-10-12 isovaleric acid
503-74-2
US $0.00 / kg 1kg 0.99 20tons Hebei Yanxi Chemical Co., Ltd.
Isovaleric acid pictures 2023-08-26 Isovaleric acid
503-74-2
US $0.00 / KG 1KG 99% 50000KG/month Hebei Mojin Biotechnology Co., Ltd
  • Isovaleric acid pictures
  • Isovaleric acid
    503-74-2
  • US $3310.00-3000.00 / Tons
  • 99.99%
  • Hebei Dangtong Import and export Co LTD
AKOS BBS-00003796 RARECHEM AL BO 0154 3-Methylbuttersαure 3-methyl-butyricaci 3-Methyl-n-butyricacid Acetic acid, isopropyl- Aceticacid,isopropyl- isopropyl-aceticaci Isopropylessigsαure isovalerianic isovalerianicacid Isovaleriansαure Kyselina isovalerova kyselinaisovalerova methyl butanoic acid 3-Methyl butancic acid ISOPENTANOIC ACID FOR SYNTHESIS Isovaleric aci Isopentanoic acid-3-Methylbutyric acid iso-Valeric acid 98+ % (acidimetric) Isovaleric acid (mixture of isomers) BETA-METHYLBUTYRIC ACID ISOPROPYLACETIC ACID FEMA 3102 ISOVALERIC ACID acideisovalerique Butyric acid, 3-methyl- Delphinic acid delphinicacid femanumber:3102 isobutylformicacid iso-C4H9COOH #niso-Valeric acid VALERIC ACID 99+% FCC ISOVALERIC ACID 98+% NATURAL ISOVALERIC ACID 99+% GC STANDARD Isovalericacid,98% isovalericacid,3-methylbutanoicacid,methylbutyricacid ISOVALERIC ACID(SG) ISOVALERICACIDANDITSCOMMONSALTS ISOVALERIANSAEURE ISOVALERIC ACID WITH GC ISOVALERIC ACID, NATURAL 3-Methylbutanoic acid, 3-Methylbutyric acid Isovaleric acid ,99% Isovleric Acid Isovaleric acid, 99% 100GR Isovaleric acid, 99% 10GR Isovaleric acid,3-Methylbutanoic acid, 3-Methylbutyric acid Isovaleric acid, synthesis grade Natural 3-Methybutyric Acid Natural Isovaleric Acid M**3-Methylbutanoic acid、Isovaleric acid IsovalericAcid> Isovaleric acid, 99%, for synthesis Isovaleric acidQ: What is Isovaleric acid Q: What is the CAS Number of Isovaleric acid Q: What is the storage condition of Isovaleric acid Q: What are the applications of Isovaleric acid Isovaleric acid 503-74-2 Iso-Valeric Acid, 98&plus