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CAS No 50-81-7 , (2R)-2-[(1S)-1,2-dihydroxyethyl]-3,4-dihydroxy-2H-furan-5-one Search by region : Germany

  • Name: (2R)-2-[(1S)-1,2-dihydroxyethyl]-3,4-dihydroxy-2H-furan-5-one
  • Synonyms: Cebione; Ascorbicap; Cecon; Cevalin; ascorbate;(2R)-2-[(1S)-1,2-dihydroxyethyl]-3,4-dihydroxy-2H-furan-5-one; vitamin C; Ascoltin; Cevex;l-ascorbic acid;
  • CAS Registry Number:
  • Melting Point: 190-192 ºC
  • Density: 1,65 g/cm3
  • Refractive index: 21 ° (C=10, H2O)
  • Alpha: 20.5 º (C=10,H2O)
  • Water Solubility: 333 G/L (20 ºC)
  • Safety Statements: S24/25
  • Hazard Symbols: Xn
  • EINECS: 200-066-2
  • Molecular Weight: 176.12412
  • InchiKey: CIWBSHSKHKDKBQ-JLAZNSOCSA-N
  • InChI: InChI=1S/C6H8O6/c7-1-2(8)5-3(9)4(10)6(11)12-5/h2,5,7-10H,1H2/t2-,
    5+/m0/s1
  • Risk Statements: S24/25
  • Molecular Formula: C6H8O6
  • Molecular Structure:CAS No:50-81-7 (2R)-2-[(1S)-1,2-dihydroxyethyl]-3,4-dihydroxy-2H-furan-5-one

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50-81-7 ASCORBIC ACID (VITAMIN C)

  • Germany Cfm Oskar Tropitzsch [Manufacturer]
  • Tel: +49-9231-9619-0
  • Fax: +49-9231-9619-60
  • Address: Cfm Oskar Tropitzsch
    Waldershofer Str. 49-51
    95615 Marktredwitz
    Germany ,Germany
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50-81-7 ASCORBIC ACID POWDERED, PURE PH. EUR., BP, USP, FOOD GRADE

  • Germany AppliChem GmbH [Manufacturer]
  • Tel: +49 6151 93 57 0
  • Fax: +49 6151 93 57 11
  • Address: AppliChem GmbH
    Ottoweg 4
    64291 Darmstadt
    Germany ,Germany
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50-81-7 ASCORBIC ACID

  • Germany Beckmann-Kenko GmbH [Manufacturer]
  • Tel: +49 4241 9308-88
  • Fax: +49 4241 9308-89
  • Address: Beckmann-Kenko GmbH
    AUF DEM SCHEUNENBRINK 8
    D-27211 BASSUM, GERMANY ,Germany
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50-81-7 Vitamin C

  • Germany Klaus F. Meyer GmbH [Manufacturers]
  • Tel: +49-(0)-62 37 - 20 23
  • Fax: +49-(0)-62 37 - 20 26
  • Address: Leiblstrasse 3, Fussgoenheim D-67136, Fussgoenheim,FussgoenheimGermany
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50-81-7 L(+)-Ascorbic acid powdered BioChemica

  • L(+)-Ascorbic acid powdered BioChemica
  • Germany AppliChem mbH []
  • Tel: +49 6151 93 57 0
  • Fax: +49 6151 93 57 11
  • Address: Ottoweg 4 D-64291 Darmstadt ,Germany
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50-81-7 ASCORBIC ACID

  • Germany Klaus F. Meyer GmbH [Manufacturer]
  • Tel: +49 (0) 62 37 - 20 23
  • Fax: +49 (0) 62 37 - 20 26
  • Address: Klaus F. Meyer GmbH
    Leiblstrasse 3
    D - 67136 Fussgoenheim
    Germany ,Germany
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50-81-7 L(+)-Ascorbic acid

  • Germany Beckmann Chemikalien KG [Manufacturers]
  • Tel: +49 4241 9308 0
  • Fax: +49-42 41/93 08-30
  • Address: Bassum,BassumGermany
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50-81-7 ASCORBIC ACID

  • Germany CEDA Chemicals GmbH [Manufacturer]
  • Tel: + 49 - 25 94 - 78 31 40 - 0
  • Fax: + 49 - 25 94 - 78 31 40 - 22
  • Address: CEDA Chemicals GmbH
    Fehrbelliner Platz 1
    D-48249 D?lmen
    Germany ,Germany
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References of (2R)-2-[(1S)-1,2-dihydroxyethyl]-3,4-dihydroxy-2H-furan-5-one
Title: Ascorbic Acid
CAS Registry Number: 50-81-7
CAS Name: L-Ascorbic acid
Synonyms: vitamin C; 3-oxo-L-gulofuranolactone; L-threo-hex-2-enonic acid g-lactone; L-3-keto-threo-hexuronic acid lactone; L-xylo-ascorbic acid; antiscorbutic vitamin; cevitamic acid
Trademarks: Ascorbicap (Valeant); Ascorbin (Montavit); Ascorvit (Jenapharm); Cantan (Aventis); Cebion (Merck KGaA); Cecon (Abbott); Celaskon (Leciva); Celin (GSK); Cetebe (GSK); Cevalin (Lilly); Ce-Vi-Sol (BMS); Cevitan (Aventis); Cewin (Sanofi-Synthelabo); C-Vimin (AstraZeneca); Hicee (Takeda); Hybrin (Pfizer); Laroscorbine (Roche); Redoxon (Roche); Ribena (GSK); Vitacimin (Takeda); Vitacin (Towa Yakuhin); Vitascorbol (Aventis)
Molecular Formula: C6H8O6
Molecular Weight: 176.12
Percent Composition: C 40.92%, H 4.58%, O 54.51%
Literature References: Physiological antioxidant. Coenzyme for a number of hydroxylation reactions; required for collagen synthesis. Widely distributed in plants and animals. Most primates (including humans), guinea pigs, and some birds and fish cannot synthesize ascorbic acid. Inadequate intake results in deficiency syndromes such as scurvy. Dietary sources include citrus fruits, potatoes, peppers, broccoli, cabbage, and rose hips. First isolated from the adrenal cortex of ox and later from lemons and paprika (originally called hexuronic acid): A. Szent-Gy?rgyi, Biochem. J. 22, 1387 (1928); W. N. Haworth, A. Szent-Gy?rgyi, Nature 131, 24 (1933). Structure studies: R. W. Herbert et al., J. Chem. Soc. 1933, 1270. Synthesis: R. G. Ault et al., ibid. 1419; T. Reichstein et al., Helv. Chim. Acta 16, 561, 1019 (1933); 17, 311, 510 (1934). Review of discovery, structure and synthesis: E. L. Hirst, Fortschr. Chem. Org. Naturst. 2, 132-159 (1939). Crystal structure: J. Hvoself, Acta Chem. Scand. 18, 841 (1964). Review of syntheses: T. C. Crawford, S. A. Crawford, Adv. Carbohydr. Chem. 37, 79-155 (1980). HPLC determn in plasma: J. Lykkesfeldt et al., Anal. Biochem. 229, 329 (1995). Discussion of use in the treatment of the common cold: L. Pauling, Proc. Natl. Acad. Sci. USA 68, 2678 (1971); H. Hemil?, Scand. J. Infect. Dis. 26, 1 (1994). Clinical applications in immunology, lipid metabolism and cancer: Int. J. Vitam. Nutr. Res. 1982, Suppl. 23, 294 pp. Comprehensive description: I. A. Al-Meshal, M. M. A. Hassan, Anal. Profiles Drug Subs. 11, 45-78 (1982). Reviews: G. M. Jaffe in Kirk-Othmer Encyclopedia of Chemical Technology vol. 24 (John Wiley & Sons, New York, 3rd Ed., 1984) pp 8-40; "Vitamin C" in Vitamins, W. Friedrich, Ed. (Walter de Gruyter, Berlin, 1988) pp 929-1001. Review of pharmacology and clinical applications: M. Levine, N. Engl. J. Med. 314, 892-902 (1986); H. E. Sauberlich, Annu. Rev. Nutr. 14, 371-391 (1994).
Properties: Crystals (usually plates, sometimes needles, monoclinic system). Pleasant, sharp acidic taste. mp 190-192° (some dec). d 1.65. [a]D25 +20.5 to +21.5° (c = 1 in water); [a]D23 +48° (c = 1 in methanol). pH = 3 (5 mg/ml); pH = 2 (50 mg/ml); pK1 = 4.17; pK2 = 11.57. uv max at pH 2: 245 nm (E1%1cm 695); at pH 6.4: 265 nm (E1%1cm 940). Redox potential (first stage): E10 +0.166 V (pH 4). One gram dissolves in about 3 ml water, 30 ml alc, 50 ml abs alc, 100 ml glycerol, 20 ml propylene glycol. Soly in water: 80.0% at 100°; 40.0% at 45°. Insol in ether, chloroform, benzene, petr ether, oils, fats, fat solvents. Strong reducing agent. Stable to air when dry; aq solns are rapidly oxidized by air.
Melting point: mp 190-192° (some dec)
pKa: pK1 = 4.17; pK2 = 11.57
Optical Rotation: [a]D25 +20.5 to +21.5° (c = 1 in water); [a]D23 +48° (c = 1 in methanol)
Absorption maximum: uv max at pH 2: 245 nm (E1%1cm 695); at pH 6.4: 265 nm (E1%1cm 940)
Density: d 1.65
 
Derivative Type: Calcium hypophosphite
Synonyms: Asphocalcium
Trademarks: Calscorbat (Aerocid)
Molecular Formula: C6H9CaO8P
Molecular Weight: 280.18
Percent Composition: C 25.72%, H 3.24%, Ca 14.30%, O 45.68%, P 11.05%
 
Derivative Type: Calcium salt
CAS Registry Number: 5743-27-1
Synonyms: Calcium ascorbate
Molecular Formula: C12H14CaO12
Molecular Weight: 390.31
Percent Composition: C 36.93%, H 3.62%, Ca 10.27%, O 49.19%
Literature References: Prepn: Ruskin, Merrill, Science 105, 504 (1947).
Properties: Dihydrate, triclinic crystals, [a]D20 +95.6° (c = 2.4). Freely sol in water. Practically insol in methanol, ethanol.
Optical Rotation: [a]D20 +95.6° (c = 2.4)
 
Derivative Type: Sodium salt
CAS Registry Number: 134-03-2
Synonyms: Sodium ascorbate
Trademarks: Cenolate (Abbott); Xitix (Woelm)
Molecular Formula: C6H7NaO6
Molecular Weight: 198.11
Percent Composition: C 36.38%, H 3.56%, Na 11.60%, O 48.46%
Literature References: Prepn: Holland, US 2442005 (1948).
Properties: Minute crystals, dec 218°. [a]D20 +104.4°. Soly in water: 62 g/100 ml at 25°; 78 g/100 ml at 75°.
Optical Rotation: [a]D20 +104.4°
 
Use: As antimicrobial and antioxidant in foodstuffs.
Therap-Cat: Vitamin (antiscorbutic).
Therap-Cat-Vet: Vitamin (antiscorbutic).
Keywords: Vitamin/Vitamin Source; Vitamin C.