CAS:110-94-1 C5H8O4 1,5-Pentanedioic acid
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| 500 Gram |
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- Min.Order :500 Gram
- Purity: 99%
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Keywords
CAS:110-94-1 C5H8O4 1,5-Pentanedioic acid CAS:110-94-1 C5H8O4 factory price high purity 99% CAS:110-94-1 C5H8O4 technical grade or OLED grade
Quick Details
- Appearance:white poweder
- Application:CAS:110-94-1 C5H8O4 technical grade or OLED grade
- PackAge:Plastic vacuum packaging bag or bucket
- ProductionCapacity:1|Metric Ton|Day
- Storage:under the cool and dry area
- Transportation:by express or by sea
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| 1,5-Pentanedioic acid Basic information |
| Product Name: | 1,5-Pentanedioic acid |
| Synonyms: | a,-Propanedicarboxylicacid;glutaric;Glutarsaure;1,3-PROPANEDICARBOXYLIC ACID;1,5-PENTADIOIC ACID;1,5-PENTANEDIOIC ACID;GLUTARIC ACID AND ANHYDRIDE;GLUTARIC ACID |
| CAS: | 110-94-1 |
| MF: | C5H8O4 |
| MW: | 132.11 |
| EINECS: | 203-817-2 |
| Product Categories: | Pharmaceutical Intermediates;alpha,omega-Alkanedicarboxylic Acids;alpha,omega-Bifunctional Alkanes;Monofunctional & alpha,omega-Bifunctional Alkanes;C1 to C5;Carbonyl Compounds;Carboxylic Acids |
| Mol File: | 110-94-1.mol |
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| 1,5-Pentanedioic acid Chemical Properties |
| mp | 95-98 °C(lit.) |
| bp | 302 °C |
| density | 1,429 g/cm3 |
| Fp | 200°C/20mm |
| storage temp. | 2-8°C |
| Water Solubility | 430 g/L (20 ºC) |
| Merck | 14,4473 |
| BRN | 1209725 |
| Stability: | Stable. Incompatible with bases, oxidizing agents, reducing agents. |
| CAS DataBase Reference | 110-94-1(CAS DataBase Reference) |
| NIST Chemistry Reference | Pentanedioic acid(110-94-1) |
| EPA Substance Registry System | Pentanedioic acid(110-94-1) |
| Safety Information |
| Hazard Codes | Xi |
| Risk Statements | 36-36/37/38 |
| Safety Statements | 26-37/39-36 |
| WGK Germany | 1 |
| RTECS | MA3740000 |
| HS Code | 29171990 |
| Hazardous Substances Data | 110-94-1(Hazardous Substances Data) |
| 1,5-Pentanedioic acid Usage And Synthesis |
| Chemical Properties | white or off-white crystals |
| General Description | Colorless crystals or white solid. |
| Air & Water Reactions | Water soluble. |
| Reactivity Profile | 1,5-Pentanedioic 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 1,5-Pentanedioic 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 1,5-Pentanedioic acid reacts with bases, oxidizing agents and reducing agents. |
| Fire Hazard | Flash point data for 1,5-Pentanedioic acid are not available; however, 1,5-Pentanedioic acid is probably combustible. |
| 1,5-Pentanedioic acid Preparation Products And Raw materials |
| Preparation Products | Buspirone-->Cinmethylin-->Glutaric anhydride-->Azelaic acid-->LACCAIC ACID-->Baclofen |
| Raw materials | Nitric acid-->Ammonium chloride -->POTASSIUM CYANIDE-->Cyclohexanone-->Paraffin wax-->Adipic acid-->Cyclopentanone-->gamma-Butyrolactone-->1,3-Propanediol-->NITROGEN DIOXIDE-->2,3-Dihydrofuran-->Glutaronitrile-->oxidized paraffin(wax) |
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Details:
| Name: | Glutaric Acid |
| CAS: | 110-94-1 |
| Structural Formula: |
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| Content: | Purity:≥99% |
| Packing: | Packing：25KG/Drum |
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