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| | トリス(2-カルボキシエチル)ホスフィン塩酸塩 製品概要 |
| | トリス(2-カルボキシエチル)ホスフィン塩酸塩 物理性質 |
| 融点 | 177 °C | | 比重(密度) | 1.041 g/mL at 25 °C | | 屈折率 | n20/D 1.367 | | 貯蔵温度 | 2-8°C | | 溶解性 | H2O: 50 mg/mL | | 外見 | powder | | 酸解離定数(Pka) | 7.66(at 25℃) | | 色 | white | | PH | 7.0(aqueous solution; pH was adjusted with ammonium hydroxide) | | 水溶解度 | Soluble in water and methanol. | | Sensitive | Moisture Sensitive | | 極大吸収波長 (λmax) | λ: 260 nm Amax: 0.05
λ: 280 nm Amax: 0.03 | | Merck | 14,9085 | | BRN | 3724376 | | 安定性： | Stable for 1 year from date of purchase as supplied. Solutions in distilled water may be stored at -20°C for up to 1 month. | | InChIKey | PBVAJRFEEOIAGW-UHFFFAOYSA-N | | CAS データベース | 51805-45-9(CAS DataBase Reference) |
| | トリス(2-カルボキシエチル)ホスフィン塩酸塩 Usage And Synthesis |
| 外観 | 液体 | | 使用上の注意 | 窒素封入。 | | 使用上の注意 | 不活性ガス封入 | | 説明 | TCEP HCl (51805-45-9) is a reagent for selective reduction of disulfides in aqueous solutions1-3?with distinct advantages over DTT which are application specific3. For example, spin labels are more stable with TCEP than DTT, Ni2+?(leached from affinity columns) causes rapid oxidation of DTT with no effect on TCEP and for long term storage of proteins TCEP is more stable than DTT with no metal chelator (EGTA) present but DTT is more stable in the presence of metal chelators.3 | | 化学的特性 | White Crystalline Solid | | 使用 | Reducing agent, specific for disulfidesTris(2-carboxyethyl)phosphine hydrochloride is widely used as a reducing agent to reduce disulfide bonds in proteins and trans-4,5-dihydroxy-1,2-dithiane. It is involved in the reduction of sulfoxides, sulfonyl chlorides, N-oxides, and azides. It plays an important role in the tissue homogenization process for RNA isolation. It acts as a chelating agent and forms complexes with various heavy metal ions such as Zn(II), Cd(II), Pb(II), and Ni(II). Furthermore, it is useful in the labeling of cysteine residues with maleimides. | | 使用 | TCEP (Tris(2-carboxyethyl)phosphine hydrochloride) is an alternative which is not pungent, more stable and works even at low pH. It is more selective, i.e. do not reduce metals and buried disulfides. | | 使用 | Biochemical tool for selective reduction of disulfide bridges at low pH; reductant for redox assays. | | 製造方法 | The preparation of Tris(2-carboxyethyl)phosphine hydrochloride is as follows:Trimethyl 3,3 ', 3 "-phosphine triphenylpropionate (92.5g, 0.28mol) prepared as described above was added to a 250 ml reaction flask under mechanical stirring conditions and a molar ratio of 12mol/(120ml, 1.44mol), the mixture was heated to 90°C, the solid gradually dissolved, continue to heat the reaction 4h, stirring and cooling with ice water, precipitation of white solid, filter, filter cake with distilled water to get white (2-carboxyethyl) phosphine hydrochloride, dried, weighing 61.3g, yield 82.4% | | 一般的な説明 | Tris (2-carboxyethyl) phosphine (TCEP) is very effective in cleaving disulfide bonds in aqueous solution. It dissolves in water and is odorless, unlike other trialkylphosphines (tributylphosphine). It is also less toxic than 2-mercaptoethanol. These advantages make it better than the other reducing agents. | | 反応プロフィール | Nucleophilic Substitution by the Phosphorus Atom of TCEP. 1. The phosphorus atom attacks one sulfur atom along the S-S bond. 2. A thioalkoxyphosphonium cation and a sulfhydryl anion are formed. 3. A rapid hydrolysis releases the second sulfhydryl molecule and the phosphine oxide. There are two main steps in the breaking of disulfide bridges and forming a free sulfhydryl using TCEP: cleavage of the S-S bond; oxidation of the phosphine and release of sulfhydryl.
| | Biochem/physiol Actions | Tris(2-carboxyethyl)phosphine hydrochloride solution reduces the disulfide bonds and leaves other functional groups intact in proteins. | | 貯蔵 | Following reconstitution, aliquot and freeze (-20°C). TCEP retains stability when stored at an acidic or alkaline pH; avoid storage at pH 7.0-8.0. Also avoid exposure to high concentrations of phosphate ions (>150 mM). Stock solutions are stable for up to 3 months at -20°C. | | 参考文献 | 1) Fischer?et al.?(1993),?In situ reduction suitable for matrix-assisted laser desorption/ionization and liquid secondary ionization using tris(2-carboxyethyl)phosphine; Rapid Commun. Mass Spectrom.,?7?225
2) Kirley?et al.?(1989),?Reduction and fluorescent labeling of cyst(e)ine-containing proteins for subsequent structural analysis; Anal. Biochem.,?180?231
3) Getz?et al. (1999),?A comparison between the sulfhydryl reductants tris(2-carboxyethyl)phosphine and dithiothreitol for use in protein biochemistry; Anal. Biochem.,?273?73 |
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