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| CAS番号. | 110-94-1 |
| 化学名: | グルタル酸 |
| 别名: | グルタル酸;グルタル酸 (約4.3mol/L 水溶液);n-ピロ酒石酸;ペンタン二酸;1,3-プロパンジカルボン酸;グルタール酸;グルタル酸 (約50%水溶液, 約4.3mol/L) |
| 英語化学名: | 1,5-Pentanedioic acid |
| 英語别名: | glutaric;Glutarsure;Glutarsaure;GLUTARIC ACID;Pentandioic acid;propane-1,3-dica;PENTANEDIOIC ACID;Glutaric acid,99%;Glutaric acid 99%;GLUTARIC ACID pure |
| CBNumber: | CB7852828 |
| 分子式: | C5H8O4 |
| 分子量: | 132.11 |
| MOL File: | 110-94-1.mol |
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| グルタル酸 物理性質 |
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| 安定性：: |
Stable. Incompatible with bases, oxidizing agents, reducing agents. |
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グルタル酸 化学特性,用途語,生産方法 |
化学的特性
white or off-white crystals |
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一般的な説明
Colorless crystals or white solid. |
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反応プロフィール
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. |
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火災危険
Flash point data for 1,5-Pentanedioic acid are not available; however, 1,5-Pentanedioic acid is probably combustible. |
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| グルタル酸 生産企業 Global( 204)Suppliers |
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110-94-1
a,-Propanedicarboxylicacid
glutaric
Glutarsaure
1,3-PROPANEDICARBOXYLIC ACID
1,5-PENTADIOIC ACID
1,5-PENTANEDIOIC ACID
GLUTARIC ACID AND ANHYDRIDE
GLUTARIC ACID
DICARBOXYLIC ACID C5
N-PYROTARTARIC ACID
PROPANE-1,3-DICARBOXYLIC ACID
PENTANEDIOIC ACID
Pentandioic acid
RARECHEM AL BO 0175
Glutaric acid,(Pentanedioic acid
propane-1,3-dica
Glutaric Acid, Reagent
Propane-1,5-dicarboxylic acid
Pentanedioic acid,Glutaric acid
Glutarsure
Glutaric Acid (ca. 50% in Water, ca. 4.3mol/L)
GLUTARIC ACID pure
Glutaric acid,99%
Pentanedioic Acid
1,3-Propanedicarboxylic Acid
GLUTARIC ACID FOR SYNTHESIS 250 G
GLUTARIC ACID FOR SYNTHESIS 1 KG
GLUTARIC ACID FOR SYNTHESIS 100 G
Glutaric acid 99%
Glutaric acid, Standard for GC,>99.9%(GC)
グルタル酸
グルタル酸 (約4.3mol/L 水溶液)
n-ピロ酒石酸
ペンタン二酸
1,3-プロパンジカルボン酸
グルタール酸
グルタル酸 (約50%水溶液, 約4.3mol/L)
構造分類
官能性 & α,ω-二官能性アルカン
α,ω-アルカンジカルボン酸
α,ω-二官能性アルカン
代謝産物
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