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Merck

C4805

Sigma-Aldrich

β-环糊精

powder, BioReagent, suitable for cell culture, ≥97%

别名:

Schardinger β-Dextrin, 环七淀粉, 环糊精, 环麦芽七糖

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About This Item

经验公式(希尔记法):
C42H70O35
CAS号:
分子量:
1134.98
Beilstein:
78623
EC號碼:
MDL號碼:
分類程式碼代碼:
12352201
PubChem物質ID:
NACRES:
NA.77

無菌

non-sterile

品質等級

產品線

BioReagent

化驗

≥97%

形狀

powder

光學活性

[α]20/D +162±3°, c = 1.5% in H2O

技術

cell culture | mammalian: suitable

mp

290-300 °C (dec.) (lit.)

溶解度

1 M NaOH: 50 mg/mL

運輸包裝

ambient

儲存溫度

room temp

SMILES 字串

OC[C@H]1O[C@@H]2O[C@H]3[C@H](O)[C@@H](O)[C@H](O[C@@H]3CO)O[C@H]4[C@H](O)[C@@H](O)[C@H](O[C@@H]4CO)O[C@H]5[C@H](O)[C@@H](O)[C@H](O[C@@H]5CO)O[C@H]6[C@H](O)[C@@H](O)[C@H](O[C@@H]6CO)O[C@H]7[C@H](O)[C@@H](O)[C@H](O[C@@H]7CO)O[C@H]8[C@H](O)[C@@H](O)[C@H](O[C@@H]8CO)O[C@H]1[C@H](O)[C@H]2O

InChI

1S/C42H70O35/c43-1-8-29-15(50)22(57)36(64-8)72-30-9(2-44)66-38(24(59)17(30)52)74-32-11(4-46)68-40(26(61)19(32)54)76-34-13(6-48)70-42(28(63)21(34)56)77-35-14(7-49)69-41(27(62)20(35)55)75-33-12(5-47)67-39(25(60)18(33)53)73-31-10(3-45)65-37(71-29)23(58)16(31)51/h8-63H,1-7H2/t8-,9-,10-,11-,12-,13-,14-,15-,16-,17-,18-,19-,20-,21-,22-,23-,24-,25-,26-,27-,28-,29-,30-,31-,32-,33-,34-,35-,36-,37-,38-,39-,40-,41-,42-/m1/s1

InChI 密鑰

WHGYBXFWUBPSRW-FOUAGVGXSA-N

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相关类别

應用

ββ-环糊精(β-CD)已用于合成单-6-对甲苯磺酰-CD。它还作为无血清培养基组分,用于评估大鼠嗜碱性白血病细胞吞噬纳米颗粒涉及的(细胞膜)胆固醇依赖机制。

生化/生理作用

ββ-环糊精是葡萄糖的环状α七聚物。它可形成包合物容纳多种组分,包括苯衍生物、环己烷、金刚烷、其他脂环族以及无机分子或离子。它常用于溶解非极性化合物,如脂肪酸、脂质和胆固醇。

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 1

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)


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Synthesis of mono-6-tosyl-beta-cyclodextrin, a key intermediate for the functional cyclodextrin derivatives
Tan T, et al.
Protocol Exchange (2011)
Labeling and exocytosis of secretory compartments in RBL mastocytes by polystyrene and mesoporous silica nanoparticles
Ekkapongpisit M, et al.
International journal of nanomedicine, 7, 1829-1829 (2012)
Space filling of beta-cyclodextrin and beta-cyclodextrin derivatives by volatile hydrophobic guests
Fourmentin S, et al.
Beilstein Journal of Organic Chemistry, 9(1), 1185-1191 (2013)
Mayur Sangwai et al.
International journal of pharmaceutics, 453(2), 423-432 (2012-09-01)
Despite of advancements in dosage form design and use of multifunctional excipients, improvement in dissolution characteristics of molecules like Telmisartan (TEL) having exceedingly pH dependent and poor solubility profile is still challenging. The present research work explores an innovative particle
Shuye Wang et al.
Journal of chromatography. A, 1277, 84-92 (2013-01-12)
Methoxyethylamine monosubstituted β-cyclodextrin, mono-6(A)-(2-methoxyethyl-1-ammonium)-6(A)-β-cyclodextrin chloride (MEtAMCD), is synthesized and analytically characterized. Bearing a methoxy group in cyclodextrin rim, MEtAMCD exhibits outstanding enantioselectivities toward ampholytic and acidic racemates in capillary electrophoresis. Driven by inclusion complexation, electrostatic interactions and/or hydrogen bonding, the

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