Cycloheptapentylose

β-Cyclodextrin Struktur
7585-39-9
CAS-Nr.
7585-39-9
Bezeichnung:
Cycloheptapentylose
Englisch Name:
β-Cyclodextrin
Synonyma:
β-Cyclodextrin;betadex;B-Cyclodextrin;Cyclodextrins;CARAWAY;BCD;BETA BYCLODEXTRIN;CYCLOMALTOHEPTAOSE;Β-CycIodextrin;Beta Chitosan
CBNumber:
CB8289713
Summenformel:
C42H70O35
Molgewicht:
1134.99
MOL-Datei:
7585-39-9.mol

Cycloheptapentylose Eigenschaften

Schmelzpunkt:
290-300 °C (dec.) (lit.)
alpha 
[α]D25 +159~+165° (c=1, H2O) (After Drying)
Siedepunkt:
844.96°C (rough estimate)
Dichte
1.2296 (rough estimate)
Brechungsindex
1.7500 (estimate)
FEMA 
4028 | BETA-CYCLODEXTRIN
storage temp. 
room temp
Löslichkeit
1 M NaOH: 50 mg/mL
Aggregatzustand
powder
pka
11.73±0.70(Predicted)
Farbe
white
PH
5.0-8.0 (1% in solution, Ph Eur)
Geruch (Odor)
at 100.00 %. odorless
Geruchsart
odorless
Optische Aktivität
[α]20/D +162±3°, c = 1.5% in H2O
Wasserlöslichkeit
Soluble in water and ammonium hydroxide.
Merck 
14,2718
BRN 
78623
Stabilität:
Stable. Incompatible with strong oxidizing agents.
LogP
-9.06
EPA chemische Informationen
.beta.-Cyclodextrin (7585-39-9)
Sicherheit
  • Risiko- und Sicherheitserklärung
  • Gefahreninformationscode (GHS)
Kennzeichnung gefährlicher Xi
R-Sätze: 36/37/38-20
S-Sätze: 26-36-24/25
WGK Germany  2
RTECS-Nr. GU2293000
TSCA  Yes
HS Code  29400000
Bildanzeige (GHS) GHS hazard pictograms
Alarmwort Warnung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H332 Gesundheitsschädlich bei Einatmen. Akute Toxizität inhalativ Kategorie 4 Warnung P261, P271, P304+P340, P312
Sicherheit
P261 Einatmen von Staub vermeiden.
P304+P340 BEI EINATMEN: Die Person an die frische Luft bringen und für ungehinderte Atmung sorgen.

Cycloheptapentylose Chemische Eigenschaften,Einsatz,Produktion Methoden

R-Sätze Betriebsanweisung:

R36/37/38:Reizt die Augen, die Atmungsorgane und die Haut.

S-Sätze Betriebsanweisung:

S26:Bei Berührung mit den Augen sofort gründlich mit Wasser abspülen und Arzt konsultieren.
S36:DE: Bei der Arbeit geeignete Schutzkleidung tragen.

Chemische Eigenschaften

white powder

Occurrence

A derivative of naturally occurring starch.

Verwenden

β-Cyclodextrin is a cyclic oligosaccharide produced from starch via enzymatic conversion. β-Cyclodextrin is commonly used to produce HPLC columns allowing chiral enantiomers separation.

synthetische

Usually produced commercially from Bacillus macerans or B. circulans fermentation of starch or starch hydrolysate.

Vorbereitung Methode

Cyclodextrins are manufactured by the enzymatic degradation of starch using specialized bacteria. For example, β-cyclodextrin is produced by the action of the enzyme cyclodextrin glucosyltransferase upon starch or a starch hydrolysate. An organic solvent is used to direct the reaction that produces β-cyclodextrin, and to prevent the growth of microorganisms during the enzymatic reaction. The insoluble complex of β-cyclodextrin and organic solvent is separated from the noncyclic starch, and the organic solvent is removed in vacuo so that less than 1 ppm of solvent remains in the β-cyclodextrin. The β-cyclodextrin is then carbon treated and crystallized from water, dried, and collected.

Essential oil composition

In addition to carvone, the oil contains d-limonene, carveol, diacetyl furfural, methyl alcohol, acetic aldehyde and other substances. Caraway oil consists of 3.5 to 7% volatile and fatty oils; resin, sugar, tannin, mucilage.

Allgemeine Beschreibung

Beta-Cyclodextrin is the most abundant and cheap cyclic oligosaccharide that forms inclusion complexes with several drug molecules. Its main application is in tablet and capsule formulations.
Pharmaceutical secondary standards for application in quality control, provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards.

Sicherheit(Safety)

Cyclodextrins are starch derivatives and are mainly used in oral and parenteral pharmaceutical formulations. They are also used in topical and ophthalmic formulations.
Cyclodextrins are also used in cosmetics and food products, and are generally regarded as essentially nontoxic and nonirritant materials. However, when administered parenterally, β-cyclodextrin is not metabolized but accumulates in the kidneys as insoluble cholesterol complexes, resulting in severe nephrotoxicity.
Cyclodextrin administered orally is metabolized by microflora in the colon, forming the metabolites maltodextrin, maltose, and glucose; these are themselves further metabolized before being finally excreted as carbon dioxide and water. Although a study published in 1957 suggested that orally administered cyclodextrins were highly toxic, more recent animal toxicity studies in rats and dogs have shown this not to be the case, and cyclodextrins are now approved for use in food products and orally administered pharmaceuticals in a number of countries.
Cyclodextrins are not irritant to the skin and eyes, or upon inhalation. There is also no evidence to suggest that cyclodextrins are mutagenic or teratogenic.
β-Cyclodextrin
LD50 (mouse, IP): 0.33 g/kg(16)
LD50 (mouse, SC): 0.41 g/kg
LD50 (rat, IP): 0.36 g/kg
LD50 (rat, IV): 1.0 g/kg
LD50 (rat, oral): 18.8 g/kg
LD50 (rat, SC): 3.7 g/kg

Lager

Cyclodextrins should be stored in a tightly sealed container, in a cool, dry place.Cyclodextrins are stable in the solid state if protected from high humidity.

läuterung methode

Recrystallise β-cyclodextrin from water and dry it for 12hours in a vacuum at 110o, or 24hours in a vacuum at 70o. The purity is assessed by TLC on cellulose containing a fluorescent indicator. [Taguchi, J Am Chem Soc 108 2705 1986, Tabushi et al. J Am Chem Soc 108 4514 1986, Orstam & Ross J Phys Chem 91 2739 1987.] [Beilstein 19 IV 6287, 19/12 V 801.]

Regulatory Status

Included in the FDA Inactive Ingredients Database: α-cyclodextrin (injection preparations); β-cyclodextrin (oral tablets, topical gels); γ-cyclodextrin (IV injections).
Included in the Canadian List of Acceptable Non-medicinal Ingredients (stabilizing agent; solubilizing agent ); and in oral and rectal pharmaceutical formulations licensed in Europe, Japan, and the USA.

Cycloheptapentylose Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


Cycloheptapentylose Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

Global( 606)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
Hefei TNJ Chemical Industry Co.,Ltd.
0551-65418684 +8618949823763
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Henan Allgreen Chemical Co.,LTD
+86-37155567971 +86-13633837469
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Sigma Audley
+86-18336680971 +86-18126314766
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7585-39-9(Cycloheptapentylose)Verwandte Suche:


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