推荐产品
化驗
99%
mp
155-158 °C (lit.)
SMILES 字串
OC(=O)CCSSCCC(O)=O
InChI
1S/C6H10O4S2/c7-5(8)1-3-11-12-4-2-6(9)10/h1-4H2,(H,7,8)(H,9,10)
InChI 密鑰
YCLSOMLVSHPPFV-UHFFFAOYSA-N
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一般說明
3,3′-二硫代二丙酸通过自组装程序在多晶金电极上形成单层,以形成金3,3′-二硫代二丙酸自组装单层修饰电极。它是合成含3-巯基丙酸的聚硫酯的前体物质。它作为主要碳补充剂被添加到新型β变形杆菌菌株DPN7的培养基中。
應用
使用3,3′-二硫代二丙酸可作为封端剂,用于在金纳米颗粒表面上引入电荷。
訊號詞
Warning
危險聲明
危險分類
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
11 - Combustible Solids
水污染物質分類(WGK)
WGK 3
閃點(°F)
Not applicable
閃點(°C)
Not applicable
個人防護裝備
dust mask type N95 (US), Eyeshields, Gloves
其他客户在看
Journal of chromatography. A, 1167(1), 35-41 (2007-09-07)
We employed agarose gel preparative electrophoresis to separate gold nanoparticles based on size, shape, and charge. The separating technique was first demonstrated by size separation of 5 nm, 15 nm, and 20 nm spherical gold nanoclusters; and further evidenced through
Talanta, 72(2), 427-433 (2007-04-30)
Monolayers of 3,3'-dithiodipropionic acid (DTDPA) were prepared on a polycrystalline gold electrode through a self-assembly procedure to produce a gold 3,3'-dithiodipropionic acid self-assembled monolayer (AuDTDPA) modified electrode. The characterization of the AuDTDPA electrode was investigated by cyclic voltammetry and ac
Macromolecular bioscience, 16(3), 420-431 (2015-12-10)
In this article, the low-molecular weight biodegradable methoxy poly (ethylene glycol)-poly (D,L-lactide-co-glycolide) (PP) is chosen as polymeric skeleton to be conjugated with docetaxel (DTX) by disulfide bond (PP-SS-DTX) to construct the reduction-sensitive drug delivery system. The conjugates are synthesized via
International journal of pharmaceutics, 534(1-2), 368-377 (2017-10-21)
P-glycoprotein (P-gp) is a major efflux transporter overexpressed on multidrug resistant tumor cells and responsible for pumping drugs out. If anti-tumor drugs are given when P-gp level is low, satisfactory treatment efficiency may be achieved. Thus, a P-gp down-regulating siRNA
Colloids and surfaces. B, Biointerfaces, 155, 41-50 (2017-04-14)
Stimuli-responsive nanocarriers for anticancer drug and gene co-delivery are promising strategy in cancer therapy. The ultimate goal is to deliver high local concentration of therapeutic agents with no premature release and result in synergistic effects for combination therapies. In this
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