購物車 
-
Decyl D-glucoside
- names：
(3R,4S,5S,6R)-2-(decyloxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol
- CAS號：
54549-25-6
MDL Number： - MF(分子式)： C16H32O6 MW(分子量)： 320.43
- EINECS: Reaxys Number:
- Pubchem ID: Brand:BIOFOUNT
| 貨品編碼 | 規格 | 純度 | 價格 (￥) | 現價(￥) | 特價(￥) | 庫存描述 | 數量 | 總計 (￥) |
|---|
| 中文別名 | Decyl D-glucoside |
| 英文別名 | Decyl D-glucoside; decyl D-glucopyranoside; decyl D-glucoside; decyl dextro-glucoside; D- glucopyranoside, decyl. |
| CAS號 | 54549-25-6 |
| Inchi | InChI=1S/C16H32O6/c1-2-3-4-5-6-7-8-9-10-21-16-15(20)14(19)13(18)12(11-17)22-16/h12-20H,2-11H2,1H3/t12-,13-,14+,15-,16?/m1/s1 |
| InchiKey | JDRSMPFHFNXQRB-IWQYDBTJSA-N |
| 分子式 Formula | C16H32O6 |
| 分子量 Molecular Weight | 320.43 |
| 溶解度Solubility | |
| 性狀 | Solid powder |
| 儲藏條件 Storage conditions | Dry, dark and store at 0-4℃ for short term (days to weeks) or -20℃ for long term (Store correctly 2-3years). |
| 產品說明 | Decyl D-glucoside(CAS:54549-25-6):僅限應用于工業或者科學研究過程中非醫療目的，不應用于人類或動物的臨床診斷以及治過程療，該產品非藥用，非食用。 |
| Introduction | Decyl glucoside or decyl d-glucoside, also named decylbeta- d-glucopyranoside, belongs to the alkyl glucosides family and is obtained by condensation of the fatty alcohol decyl alcohol and a d-glucose polymer. This nonionic surfactant and cleansing agent has been widely used for several years, due to its foaming power and good tolerance in rinse-off products such as shampoos, hair dyes and colors, and soaps. Decyl glucoside is also employed in leave-on products such as no-rinsing cleansing milks, lotions, and several sunscreen agents and is contained as a stabilizing surfactant of organic microparticles in sunscreen agent Tinosorb. |
| Application1 | |
| Application2 | |
| Application3 |
| [1]Feroz H, Kwon H, Peng J, Oh H, Ferlez B, Baker CS, Golbeck JH, Bazan GC, Zydney AL, Kumar M. Improving extraction and post-purification concentration of membrane proteins. Analyst. 2018 Mar 12;143(6):1378-1386. doi: 10.1039/c7an01470h. PubMed PMID: 29220051. |
| [2]Feroz H, Vandervelden C, Ikwuagwu B, Ferlez B, Baker CS, Lugar DJ, Grzelakowski M, Golbeck JH, Zydney AL, Kumar M. Concentrating membrane proteins using ultrafiltration without concentrating detergents. Biotechnol Bioeng. 2016 Oct;113(10):2122-30. doi: 10.1002/bit.25973. Epub 2016 Mar 28. PubMed PMID: 27563851. |
| [3] Varga I, Mészáros R, Stubenrauch C, Gilányi T. Adsorption of sugar surfactants at the air/water interface. J Colloid Interface Sci. 2012 Aug 1;379(1):78-83. doi: 10.1016/j.jcis.2012.04.053. Epub 2012 Apr 27. PubMed PMID: 22609189. |
| [4] Ishibashi A, Nakashima N. Individual dissolution of single-walled carbon nanotubes in aqueous solutions of steroid or sugar compounds and their Raman and near-IR spectral properties. Chemistry. 2006 Oct 10;12(29):7595-602. PubMed PMID: 16927276. |
| [5] Kakehashi R, Shizuma M, Yamamura S, Takeda T. Mixed micelles containing sodium oleate: the effect of the chain length and the polar head group. J Colloid Interface Sci. 2004 Nov 1;279(1):253-8. PubMed PMID: 15380436. |
6: Hasler L, Walz T, Tittmann P, Gross H, Kistler J, Engel A. Purified lens major intrinsic protein (MIP) forms highly ordered tetragonal two-dimensional arrays by reconstitution. J Mol Biol. 1998 Jun 19;279(4):855-64. PubMed PMID: 9642066.7: Stubbs GW, Smith HG Jr, Litman BJ. Alkyl glucosides as effective solubilizing agents for bovine rhodopsin. A comparison with several commonly used detergents. Biochim Biophys Acta. 1976 Feb 19;426(1):46-56. PubMed PMID: 1247624.
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