L-threo-Hexo-2,3-diulosono-1,4-lacton

DEHYDROASCORBIC ACID Struktur
490-83-5
CAS-Nr.
490-83-5
Bezeichnung:
L-threo-Hexo-2,3-diulosono-1,4-lacton
Englisch Name:
DEHYDROASCORBIC ACID
Synonyma:
Dehydroascorbate;DEHYDRO-L-ASCORBIC ACID;BIS-DHA;C05422;ehydroascorbicaci;L-Dehydroascorbate;OXIDIZED VITAMIN C;DEHYDROASCORBIC ACID;Oxidized Ascorbic Acid;L-ASCORBIC ACID OXIDIZED
CBNumber:
CB1397000
Summenformel:
C6H6O6
Molgewicht:
174.11
MOL-Datei:
490-83-5.mol

L-threo-Hexo-2,3-diulosono-1,4-lacton Eigenschaften

Schmelzpunkt:
228 °C (dec.)(lit.)
alpha 
D20 +56°
Siedepunkt:
389.3±38.0 °C(Predicted)
Dichte
1.743±0.06 g/cm3(Predicted)
storage temp. 
-20°C
Löslichkeit
DMSO (Slightly, Heated), Methanol (Slightly, Sonicated)
Aggregatzustand
Solid
pka
3.90(at 25℃)
Farbe
White to Dark Orange
Merck 
13,2886
Stabilität:
Light Sensitive
LogP
-1.702 (est)
CAS Datenbank
490-83-5(CAS DataBase Reference)
Sicherheit
  • Risiko- und Sicherheitserklärung
  • Gefahreninformationscode (GHS)
Kennzeichnung gefährlicher Xn
R-Sätze: 22
WGK Germany  3
1-8-10
HS Code  2936270000
Bildanzeige (GHS) GHS hazard pictograms
Alarmwort Warnung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H302 Gesundheitsschädlich bei Verschlucken. Akute Toxizität oral Kategorie 4 Warnung GHS hazard pictogramssrc="/GHS07.jpg" width="20" height="20" /> P264, P270, P301+P312, P330, P501
Sicherheit
P264 Nach Gebrauch gründlich waschen.
P264 Nach Gebrauch gründlich waschen.
P270 Bei Gebrauch nicht essen, trinken oder rauchen.
P501 Inhalt/Behälter ... (Entsorgungsvorschriften vom Hersteller anzugeben) zuführen.

L-threo-Hexo-2,3-diulosono-1,4-lacton Chemische Eigenschaften,Einsatz,Produktion Methoden

Chemische Eigenschaften

Orange Solid

Verwenden

The reversibly oxidized form of ascorbic acid.

Definition

ChEBI: Dehydroascorbic acid having the L-configuration.

läuterung methode

Crystallise dehydro-L(+)-ascorbic acid from MeOH. The anhydrous acid is formed by heating it in a vacuum at 100o/1hour to give a crisp glassy product which when shaken with absolute EtOH and then kept at 0o for 2days gives microcrystals of the anhydrous acid. This is then washed with absolute EtOH and dried in a vacuum. It has m 225o(dec) and is stable in acidic solution but decomposes rapidly in alkaline solution. A 1% solution of the anhydrous acid when dissolved in phthalate/HCl buffer pH 3.5 at 60o and cooled to 20o has [] 20D +56o(0minutes), +53.5o(2hours), +19o(3days), -2o(5days) and -6o(6days); then it becomes orange in colour. A freshly prepared 1% solution in H2O has [] D +50o(0minutes), +44o(2hours), +16o(3days) and 0o(5days). [Herbert et al. J Chem Soc 1270 1933, Kenyon et al. J Chem Soc 158 1948, Beilstein 18/5 V 411.]

L-threo-Hexo-2,3-diulosono-1,4-lacton Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


L-threo-Hexo-2,3-diulosono-1,4-lacton Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

Global( 159)Lieferanten
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Henan Tianfu Chemical Co.,Ltd.
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490-83-5(L-threo-Hexo-2,3-diulosono-1,4-lacton)Verwandte Suche:


  • (5R)-5β-[(S)-1,2-Dihydroxyethyl]tetrahydrofuran-2,3,4-trione
  • C05422
  • L-Dehydroascorbate
  • L-threo-2,3-Hexodiulosonic Acid γ-Lactone
  • Oxidized Ascorbic Acid
  • L-ASCORBIC ACID OXIDIZED
  • DEHYDROASCORBIC ACID
  • DEHYDRO-L(+)-ASCORBIC ACID, DIMER
  • BIS-DEHYDRO-L-ASCORBIC ACID
  • OXIDIZED VITAMIN C
  • L-(+)-Dehydroascorbic Acid (1.24728)
  • L-threo-hexo-2,3-diulosono-1,4-lactone
  • L-threo-2,3-Hexodiulosonic acid, .gamma.-lactone
  • 5-(1,2-dihydroxyethyl)oxolane-2,3,4-trione
  • DEHYDROASCORBIC ACID(RG)
  • L-(+)-DEHYDROASCORBICACID
  • Ascorbic Acid Impurity 18
  • (5R)-5-[(1S)-12-dihydroxyethyl]oxolane-234-trione
  • L-threo-2,3-Hexodiulosonic acid, g-lactone
  • (R)-5-((S)-1,2-dihydroxyethyl)furan-2,3,4(5H)-trione
  • ehydroascorbicaci
  • DEHYDROASCORBIC ACID USP/EP/BP
  • TIANFUCHEM--High purity 490-83-5 DEHYDROASCORBIC ACID
  • Dehydroascorbate
  • DEHYDRO-L-ASCORBIC ACID
  • BIS-DHA
  • 13C6]-(L)-Dehydroascorbic acid
  • 490-83-5
  • C8H10O6
  • Specialty Synthesis
  • Monosaccharides
  • Carbohydrate Synthesis
  • KETONE
  • Carbohydrates & Derivatives
  • Intermediates & Fine Chemicals
  • Pharmaceuticals
  • Carbohydrate Synthesis
  • Monosaccharides
  • Specialty Synthesis
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