- Min.Order :10 Gram
- Purity: 99%
- Payment Terms : L/C,D/A,D/P,T/T,Other
Keywords
503-74-2 C5H10O2 Isovaleric acid 503-74-2 C5H10O2
Quick Details
- Appearance:white powder
- Application:Pharmaceutical Raw Materials;Artemisia vulgaris;Building Blocks;C1 to C5;Carbonyl Compounds;Carboxylic Acids;Carthamus tinctorius (Safflower oil);Chemical Synthesis;Humulus lupulus (Hops);Hypericum pe
- PackAge:Woven bag
- ProductionCapacity:1|Kilogram|Day
- Storage:Normal temperature
- Transportation:Ocean shipping Express delivery
Superiority:
| Isovaleric acid Basic information |
| Product Name: | Isovaleric acid |
| Synonyms: | BETA-METHYLBUTYRIC ACID;ISOPENTANOIC ACID;ISOPROPYLACETIC ACID;FEMA 3102;ISOVALERIC ACID;3-METHYLBUTANOIC ACID;3-METHYLBUTYRIC ACID;AKOS BBS-00003796 |
| CAS: | 503-74-2 |
| MF: | C5H10O2 |
| MW: | 102.13 |
| EINECS: | 207-975-3 |
| Product Categories: | Pharmaceutical Raw Materials;Artemisia vulgaris;Building Blocks;C1 to C5;Carbonyl Compounds;Carboxylic Acids;Carthamus tinctorius (Safflower oil);Chemical Synthesis;Humulus lupulus (Hops);Hypericum perforatum (St John′;Nutrition Research;Organic Building Blocks;Panax ginseng;Phytochemicals by Plant (Food/Spice/Herb);s wort) |
| Mol File: | 503-74-2.mol |
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|
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| Isovaleric acid Chemical Properties |
| mp | -35 °C |
| bp | 176 °C |
| density | 0.926 |
| vapor pressure | 0.38 mm Hg ( 20 °C) |
| FEMA | 3102 |
| refractive index |
n |
| Fp | 159 °F |
| Water Solubility | 25 g/L (20 ºC) |
| Merck | 14,5231 |
| BRN | 1098522 |
| CAS DataBase Reference | 503-74-2(CAS DataBase Reference) |
| NIST Chemistry Reference | Butanoic acid, 3-methyl-(503-74-2) |
| EPA Substance Registry System | Butanoic acid, 3-methyl-(503-74-2) |
| Safety Information |
| 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 |
| F | 13 |
| HazardClass | 6.1 |
| PackingGroup | III |
| Hazardous Substances Data | 503-74-2(Hazardous Substances Data) |
| MSDS Information |
| Provider | Language |
|---|---|
| SigmaAldrich | English |
| ACROS | English |
| ALFA | English |
| Isovaleric acid Usage And Synthesis |
| Chemical Properties | clear colorless to slightly yellow liquid |
| 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. |
| 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. |
| Isovaleric acid Preparation Products And Raw materials |
| Preparation Products | Phenvalerate-->VALERATE-->FLUCYTHRINATE-->2-(4-difluoromethoxy)phenyl-3-methyl butyric acid-->brofluthrinate-->Bromisoval-->Ethyl isovalerate |
| Raw materials | 3-Methyl-1-butanol-->Isovaleraldehyde-->MANGANESE(II) ACETATE-->VALERIAN OFFICINALIS |
Details:
| Isovaleric acid Basic information |
| Product Name: | Isovaleric acid |
| Synonyms: | BETA-METHYLBUTYRIC ACID;ISOPENTANOIC ACID;ISOPROPYLACETIC ACID;FEMA 3102;ISOVALERIC ACID;3-METHYLBUTANOIC ACID;3-METHYLBUTYRIC ACID;AKOS BBS-00003796 |
| CAS: | 503-74-2 |
| MF: | C5H10O2 |
| MW: | 102.13 |
| EINECS: | 207-975-3 |
| Product Categories: | Pharmaceutical Raw Materials;Artemisia vulgaris;Building Blocks;C1 to C5;Carbonyl Compounds;Carboxylic Acids;Carthamus tinctorius (Safflower oil);Chemical Synthesis;Humulus lupulus (Hops);Hypericum perforatum (St John′;Nutrition Research;Organic Building Blocks;Panax ginseng;Phytochemicals by Plant (Food/Spice/Herb);s wort) |
| Mol File: | 503-74-2.mol |
|
|
|
| Isovaleric acid Chemical Properties |
| mp | -35 °C |
| bp | 176 °C |
| density | 0.926 |
| vapor pressure | 0.38 mm Hg ( 20 °C) |
| FEMA | 3102 |
| refractive index |
n |
| Fp | 159 °F |
| Water Solubility | 25 g/L (20 ºC) |
| Merck | 14,5231 |
| BRN | 1098522 |
| CAS DataBase Reference | 503-74-2(CAS DataBase Reference) |
| NIST Chemistry Reference | Butanoic acid, 3-methyl-(503-74-2) |
| EPA Substance Registry System | Butanoic acid, 3-methyl-(503-74-2) |
| Safety Information |
| 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 |
| F | 13 |
| HazardClass | 6.1 |
| PackingGroup | III |
| Hazardous Substances Data | 503-74-2(Hazardous Substances Data) |
| MSDS Information |
| Provider | Language |
|---|---|
| SigmaAldrich | English |
| ACROS | English |
| ALFA | English |
| Isovaleric acid Usage And Synthesis |
| Chemical Properties | clear colorless to slightly yellow liquid |
| 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. |
| 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. |
| Isovaleric acid Preparation Products And Raw materials |
| Preparation Products | Phenvalerate-->VALERATE-->FLUCYTHRINATE-->2-(4-difluoromethoxy)phenyl-3-methyl butyric acid-->brofluthrinate-->Bromisoval-->Ethyl isovalerate |
| Raw materials | 3-Methyl-1-butanol-->Isovaleraldehyde-->MANGANESE(II) ACETATE-->VALERIAN OFFICINALIS |
HenNan sunlake enterprise corporation is located in Henan Province , The central plain of China , Which enjoys favorable geogeaphical position and convenient transportion, The com[any was established in june. 1998 , until now having more than 18 years experience in manufacturing & exporting chemical raw material .
Sunlake is a professional manufacturer engaged in producing and selling chemicals,including Organic & inorganic chemicals , pigments & Dyestuffs , Water treatment chemicals , Food & FEED additives and others . these products have been being well exported to europe , southeast Asia , the Middle East , Africa , South America and some other countries and areas.
We sincerely welcome foreign friends to visit our plant for cooperation. With the idea of "quality first,credit priority, Excellent service", We are highly acknowledged by customers for good quality and competitive price. More importantly , the company has a strong R & D team, who are professional engineers and scholars with Ph. D. .So we are confident to serve you better with our high - quality products and professional team.
We are taking great efforts to provide our customers with demanded goods and professional services, and continuously improve our core ability of competition and get the momentum for sustainable development, and finally make us being a reliable and professional wupplier in international market.
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