ChemicalBook > CAS DataBase List > gamma-Cyclodextrin

gamma-Cyclodextrin

Product Name
gamma-Cyclodextrin
CAS No.
17465-86-0
Chemical Name
gamma-Cyclodextrin
Synonyms
GAMMA-CYCLODEXTRIN;Resistant Dextrin;gammadex;CYCLOMALTOOCTAOSE;GCD;γ-CycL;gamma-CD;Ringdex C;schardinger;Cavasol? W8
CBNumber
CB9750405
Molecular Formula
C48H80O40
Formula Weight
1297.12
MOL File
17465-86-0.mol
More
Less

gamma-Cyclodextrin Property

Melting point:
≥300 °C
Boiling point:
845.2°C (rough estimate)
alpha 
[α]D25 +174~+179° (c=1, H2O) (After Drying)
Density 
1.2064 (rough estimate)
refractive index 
1.7500 (estimate)
Flash point:
450℃
storage temp. 
room temp
solubility 
1 M NaOH: 25 mg/mL, may be clear to slightly hazy
form 
powder
pka
11.68±0.70(Predicted)
color 
white
Odor
at 100.00?%. odorless
optical activity
[α]/D 174.0 to 180.0°
Water Solubility 
232g/L(25 ºC)
λmax
λ: 420 nm Amax: ≤0.20
Merck 
14,2718
BRN 
5725162
Stability:
Hygroscopic
InChIKey
GDSRMADSINPKSL-HSEONFRVSA-N
LogP
-12.02
EPA Substance Registry System
.gamma.-Cyclodextrin (17465-86-0)
More
Less

Safety

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36-24/25-22
WGK Germany 
2
RTECS 
GU2293080
3
HS Code 
29400000
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

Precautionary statements

P280Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P332+P313IF SKIN irritation occurs: Get medical advice/attention.

P337+P313IF eye irritation persists: Get medical advice/attention.

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
779431
Product name
γ-Cyclodextrin
Purity
produced by Wacker Chemie AG, Burghausen, Germany, ≥90.0% cyclodextrin basis (HPLC)
Packaging
1kg
Price
$386
Updated
2024/03/01
Sigma-Aldrich
Product number
1154591
Product name
Gammacyclodextrin
Purity
United States Pharmacopeia (USP) Reference Standard
Packaging
200mg
Price
$474
Updated
2024/03/01
TCI Chemical
Product number
C0869
Product name
gamma-Cyclodextrin
Purity
>99.0%(HPLC)
Packaging
5g
Price
$66
Updated
2024/03/01
TCI Chemical
Product number
C0869
Product name
gamma-Cyclodextrin
Purity
>99.0%(HPLC)
Packaging
25g
Price
$170
Updated
2024/03/01
Sigma-Aldrich
Product number
C4930
Product name
γ-Cyclodextrin
Purity
powder, BioReagent, suitable for cell culture, ≥98%
Packaging
100mg
Price
$114
Updated
2024/03/01
More
Less

gamma-Cyclodextrin Chemical Properties,Usage,Production

Chemical Properties

White powder or crystal

Chemical Properties

Cyclodextrins occur as white, practically odorless, fine crystalline powders, having a slightly sweet taste. Some cyclodextrin derivatives occur as amorphous powders.

Uses

A molecule used to solublize non-polar molecules such a cholesterol for use in cell culture.

Uses

γ-Cyclodextrin can be used as a precursor for the synthesis of:

  • Octakis-(2,3-di-O-methyl-6-O-carboxymethyl)-γ-cyclodextrin sodium salt (ODMCM). ODMCM is used in capillary electrophoresis as a chiral resolving agent.
  • Water-soluble cyclodextrin thioethers derivatives for the transportation of hydrophobic drugs.

Uses

γ-Cyclodextrin (γ-CD), a water-soluble cyclic oligosaccharide consisting of eight α-(1,4)-linked glucopyranose subunits, can be used in a wide range of applications including:

  • Synthesis of renewable and biocompatible metal-organic frameworks.
  • Formation of inclusion complexes with a variety of guest molecules to increase their solubility in water and other polar solvents.
  • Synthesis of γ-CD based nanogels and dendrimers as carriers and stabilizers for drug delivery applications.

Definition

ChEBI: Gamma-cyclodextrin is a cycloamylose composed of eight alpha-(1->4) linked D-glucopyranose units.

Production Methods

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.

General Description

Cyclodextrins belongs to the family of cyclic α-1,4-glucans and is made of glucose units. This molecule has a shape of a hollow cone. It possesses a hydrophilic external and hydrophobic internal surface, because of which cyclodextrins can form inclusion complexes. γ-Cyclodextrin is extensively used in food and pharmaceutical industries. Cyclodextrins are obtained by the enzymatic conversion of starch/starch derivatives by cyclodextrin glycosyltransferase.

Flammability and Explosibility

Non flammable

Pharmaceutical Applications

Cyclodextrins are ‘bucketlike’ or ‘conelike’ toroid molecules, with a rigid structure and a central cavity, the size of which varies according to the cyclodextrin type. The internal surface of the cavity is hydrophobic and the outside of the torus is hydrophilic; this is due to the arrangement of hydroxyl groups within the molecule. This arrangement permits the cyclodextrin to accommodate a guest molecule within the cavity, forming an inclusion complex.
Cyclodextrins may be used to form inclusion complexes with a variety of drug molecules, resulting primarily in improvements to dissolution and bioavailability owing to enhanced solubility and improved chemical and physical stability.
Cyclodextrin inclusion complexes have also been used to mask the unpleasant taste of active materials and to convert a liquid substance into a solid material. γ-cyclodextrin has the largest cavity and can be used to form inclusion complexes with large molecules;it has low toxicity and enhanced water solubility.
In parenteral formulations, cyclodextrins have been used to produce stable and soluble preparations of drugs that would otherwise have been formulated using a nonaqueous solvent.
In eye drop formulations, cyclodextrins form water-soluble complexes with lipophilic drugs such as corticosteroids. They have been shown to increase the water solubility of the drug; to enhance drug absorption into the eye; to improve aqueous stability; and to reduce local irritation.
Cyclodextrins have also been used in the formulation of solutions,suppositories, and cosmetics.

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.
γ-Cyclodextrin
LD50 (rat, IP): 4.6 g/kg
LD50 (rat ,IV): 4.0 g/kg
LD50 (rat, oral): 8.0 g/kg

storage

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.

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.

gamma-Cyclodextrin Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

gamma-Cyclodextrin Suppliers

Tocopharm Co., Ltd.
Tel
+86-021-69895597 13776836200 +86-13776836200
Fax
021-61292409
Email
tocopharm@gmail.com
Country
China
ProdList
187
Advantage
55
Shandong Zhiyuan Biotechnology Co., Ltd.
Tel
0543-8128041 13562317646
Fax
0543-2605568
Email
2370211093@qq.com
Country
China
ProdList
48
Advantage
58
Shangqiu Ladybug Network Technology Co., LTD
Tel
0370-2070160 19837086283
Fax
18736733639
Email
298644986@qq.com
Country
China
ProdList
2968
Advantage
58
J & K SCIENTIFIC LTD.
Tel
010-82848833 400-666-7788
Fax
86-10-82849933
Email
jkinfo@jkchemical.com
Country
China
ProdList
96815
Advantage
76
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
4006608290; 18621169109
Fax
86-21-61259102
Email
market03@meryer.com
Country
China
ProdList
40241
Advantage
62
TCI (Shanghai) Development Co., Ltd.
Tel
021-67121386
Fax
021-67121385
Email
Sales-CN@TCIchemicals.com
Country
China
ProdList
24539
Advantage
81
BeiJing Hwrk Chemicals Limted
Tel
0757-86329057 18501085097
Fax
010-89508210
Email
sales3.gd@hwrkchemical.com
Country
China
ProdList
7508
Advantage
55
Energy Chemical
Tel
021-021-58432009 400-005-6266
Fax
021-58436166
Email
sales8178@energy-chemical.com
Country
China
ProdList
44751
Advantage
61
Jia Xing Isenchem Co.,Ltd
Tel
0573-85285100 18627885956
Fax
0573-85285100
Email
isenchem@163.com
Country
China
ProdList
9555
Advantage
66
Adamas Reagent, Ltd.
Tel
400-6009262 16621234537
Fax
021-64823266
Email
zhangsn@titansci.com
Country
China
ProdList
14113
Advantage
59
More
Less

View Lastest Price from gamma-Cyclodextrin manufacturers

Henan Fengda Chemical Co., Ltd
Product
gamma-Cyclodextrin 17465-86-0
Price
US $5.00-0.10/KG
Min. Order
1KG
Purity
98%
Supply Ability
g-kg-tons, free sample is available
Release date
2024-03-26
Shandong Juchuang Chemical Co., LTD
Product
Cyclooctapentylose 17465-86-0
Price
US $51.00-25.00/kg
Min. Order
500kg
Purity
99.9
Supply Ability
200tons
Release date
2024-03-12
Hebei Jingbo New Material Technology Co., Ltd
Product
Cyclooctapentylose 17465-86-0
Price
US $0.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
10000
Release date
2023-12-25

17465-86-0, gamma-Cyclodextrin Related Search:


  • CYCLOFLO(TM) 42
  • CYCLOOCTAOSE
  • CYCLOOCTAAMYLOSE
  • CYCLOMALTOOCTAOSE
  • GAMMA-CYCLODEXTRIN
  • SCHARDINGER GAMMA-DEXTRIN
  • cyclooctapentylose
  • gamma-Cyclodextrin Produced by Wacker Chemie AG, Burghausen, Germany, Life Science, 98.0-102.0% cyclodextrin basis
  • Sugammadex Impurity 1 (Cyclooctapentylose)
  • gamma-CD
  • gammadex
  • GCD
  • Resistant Dextrin
  • GAMMA-CYCLODEXTRIN CELL CULTURE TESTED
  • schardinger
  • Cyclomaltooctaose, Cyclooctaamylose, Schardinger γ-Dextrin
  • γ-CD:Cyclooctaamylose
  • GAMMA-CYCLODEXTRIN, MIN 90%
  • gaMMa-Cyclodextrin >=98%
  • g-Cyclodextrin hydrate
  • g-Cyclodextrin standard
  • Methyl g-cyclodextrin
  • Cavasol? W8
  • Cavamax? W8
  • Cavamax(R) W8
  • ^y-Cyclodextrin hydrate
  • Gamma Cyclodextrin (200 mg)
  • Schardinger gamma-Dextrin Cyclooctaamylose
  • Alpha and gaMMa Cyclodextrin
  • gamma-Cyclodextrin produced by Wacker Chemie AG, Burghausen, Germany, >=90.0% cyclodextrin basis (HPLC)
  • Sugammadex Sodium Impurity 34
  • Cyclooctapentylose/gamma cyclodextrin
  • Gammacyclodextrin CRS
  • γ-Cyclodextrin, 98%, reagent grade
  • γ-CycL
  • Cyclooctapentylose USP/EP/BP
  • Gamma Cyclodextrien
  • Gamma yclodextrin
  • γ-Cyclodextrin, ≥98%
  • Gamma Cyclodextrin (1154591)
  • cyclooclapentylose
  • gamma-Dextrin
  • Ringdex C
  • γ-Cyclodextrin (8CI, 9CI, ACI)
  • Betadex EP Impurity B
  • Y-Cyclodextrin
  • 17465-86-0
  • C48H80O40
  • C6H10O58
  • Macrocycles for Host-Guest Chemistry
  • Cyclodextrins
  • Sugars
  • Oligosaccharides
  • BioChemical
  • Chelation/Complexation Compounds
  • Cell Signaling and Neuroscience
  • Cell Biology
  • Signal Transduction Research Tools