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Merck
CN

H3264

n-Heptyl β-D-thioglucopyranoside

≥99% (GC)

别名:

Heptyl thioglucoside, Heptyl-β-D-1-thioglucopyranoside

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关于此项目

经验公式(希尔记法):
C13H26O5S
化学文摘社编号:
分子量:
294.41
UNSPSC Code:
12352201
NACRES:
NA.25
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
6057483
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产品名称

n-Heptyl β-D-thioglucopyranoside, ≥99% (GC)

InChI key

HPEGNLMTTNTJSP-LBELIVKGSA-N

SMILES string

CCCCCCCS[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O

InChI

1S/C13H26O5S/c1-2-3-4-5-6-7-19-13-12(17)11(16)10(15)9(8-14)18-13/h9-17H,2-8H2,1H3/t9-,10-,11+,12-,13+/m1/s1

description

non-ionic

assay

≥99% (GC)

form

powder

mol wt

294.41 g/mol

technique(s)

gas chromatography (GC): suitable

color

white

CMC

30

mp

98  °C ((208 °F ))

solubility

methanol: 100 mg/mL, clear, colorless

storage temp.

−20°C

Quality Level

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Application

Useful non-ionic detergent for solubilization and reconstitution of membrane proteins.

Other Notes

To gain a comprehensive understanding of our extensive range of Monosaccharides for your research, we encourage you to visit our Carbohydrates Category page.

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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T Shimamoto et al.
Journal of biochemistry, 97(6), 1807-1810 (1985-06-01)
A new nonionic detergent, heptylthioglucoside, was synthesized and found to be more soluble than octylthioglucoside in water at low temperatures. Use of this detergent for solubilization and reconstitution of membrane proteins of Escherichia coli was examined. Heptylthioglucoside was as effective
T Ohyashiki et al.
Biochimica et biophysica acta, 902(1), 46-52 (1987-08-07)
The brush-border membrane from the porcine small intestine possesses Ca2+-dependent ATPase activity. The Ca2+ stimulation of ATP hydrolysis by the membranes is biphasic with a high affinity (Km = 0.38 microM) and a low affinity (Km = 98.3 microM). Treatment
N Sone
Journal of biochemistry, 100(6), 1465-1470 (1986-12-01)
It is possible to prepare liposomal vesicles by solubilization of total bacterial membranes with n-heptyl beta-D-thioglucoside followed by reconstitution into proteoliposomes by a freeze-thaw-sonication procedure with soybean phospholipids. The resulting proteoliposomes from total membrane fraction of sufficiently aerated cells of
K Nagai et al.
Journal of biochemistry, 101(5), 1115-1127 (1987-05-01)
Some properties of the enzyme activity that catalyzes the transfer of N-acetylgalactosamine from UDP-N-acetylgalactosamine to exogenous lactosylceramide-II3-sulfate (SM3) and N-acetylneuraminosyllactosylceramide (GM3) were studied using the enzyme preparation solubilized from the 100,000 X g pellet of 6-day-old rat brain. The products

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