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CAS No 485-47-2 , 2,2-dihydroxyindene-1,3-dione

  • Name: 2,2-dihydroxyindene-1,3-dione
  • Synonyms: 2,2-dihydroxyindene-1,3-dione; Ninhydrin hydrate; 2,2-Dihydroxy-1H-indene-1,3(2H)-dione;485-47-2; 1,2,3-Indantrione monohydrate; 2,2-Dihydroxy-1,3-indandione;
  • CAS Registry Number:
  • Transport: UN 1170 3/PG 2
  • Melting Point: 250 ºC
  • Density: 0.862
  • Water Solubility: 0.1-0.5 G/100 ML AT 20 ºC
  • Safety Statements: R22;R36/37/38
  • Hazard Symbols: Xn: Harmful;
  • EINECS: 207-618-1
  • Molecular Weight: 178.14154
  • InchiKey: FEMOMIGRRWSMCU-UHFFFAOYSA-N
  • InChI: InChI=1S/C9H6O4/c10-7-5-3-1-2-4-6(5)8(11)9(7,12)13/h1-4,12-13H
  • Risk Statements: S26;S28A
  • Molecular Formula: C9H6O4
  • Molecular Structure:CAS No:485-47-2 2,2-dihydroxyindene-1,3-dione
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485-47-2 Ninhydrin

  • India Heni Chemical Industries [Manufacturers]
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485-47-2 NINHYDRIN

  • United States CTL Scientific Supply Corp. [Manufacturer]
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485-47-2 Ninhydrin

  • China RuGao Riancheng Chemical Co.,LtD [Manufacturers]
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485-47-2 Ninhydrin

  • India Shinton Chemicals P. Ltd. [Manufacturers]
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  • Address: 93 Chandralok, Near National Tower Indore - 452 018 Madhya Pradesh, India Indore,Madhya PradeshIndia
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References of 2,2-dihydroxyindene-1,3-dione
Title: Ninhydrin
CAS Registry Number: 485-47-2
CAS Name: 2,2-Dihydroxy-1H-indene-1,3(2H)-dione
Synonyms: 2,2-dihydroxy-1,3-indanedione; 1,2,3-indantrione monohydrate; triketohydrinden hydrate
Molecular Formula: C9H6O4
Molecular Weight: 178.14
Percent Composition: C 60.68%, H 3.39%, O 35.93%
Literature References: Prepn: Ruhemann, J. Chem. Soc. 97, 1438 (1910); Teeters, Shriner, J. Am. Chem. Soc. 55, 3026 (1933); Wanag, Lode, Ber. 71, 1267 (1938). Improved syntheses: L. F. Fieser, Experiments in Organic Chemistry (Boston, 3rd ed., 1955) p 123; Becker, Russell, J. Org. Chem. 28, 1896 (1963). Absorption spectrum: Polonovski et al., Bull. Soc. Chim. [5] 6, 1557 (1939). Poisonous action on bacteria, mice, guinea pigs: O. Loew, Biochem. Z. 69, 111 (1915). Acute toxicity study: J. C. Breton et al., C.R. Seances Soc. Biol. Ses Fil. 151, 719 (1957). Monograph: Henri Plagnol, Influence de la Structure des Composés Aminés dans leur Reaction avec la Ninhydrine (Bordeaux, 1962) 156 pp. Reviews: J. C. Breton, Etudes Chimiques et Biologiques sur la Ninhydrine, Réactif des Aminoacides (Imprimerie E. Drouillard, Bordeaux, 1958) 285 pp; McCaldin, Chem. Rev. 60, 39 (1960); A. Schoenberg, E. Singer, Tetrahedron 34, 1285-1300 (1978).
 
Derivative Type: Monohydrate
Properties: Pale yellow prisms from water or alcohol. Reddens at 125°, swells at 139°, dec 241°. Freely sol in water. LD50 i.p. in mice: 78 mg/kg (Breton, 1957).
Toxicity data: LD50 i.p. in mice: 78 mg/kg (Breton, 1957)
 
Use: Reagent for the detection of free amino and carboxyl groups in proteins and peptides, yielding a blue color under the proper conditions.