T7567
Tributylphosphine solution
200 mM (in N-methyl-2-pyrrolidinone), liquid
Synonyme(s) :
TBP
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A propos de cet article
Formule empirique (notation de Hill) :
C12H27P
Numéro CAS:
Poids moléculaire :
202.32
NACRES:
NA.56
PubChem Substance ID:
UNSPSC Code:
41105323
MDL number:
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liquid
Quality Level
concentration
200 mM (in N-methyl-2-pyrrolidinone)
SMILES string
CCCCP(CCCC)CCCC
InChI
1S/C12H27P/c1-4-7-10-13(11-8-5-2)12-9-6-3/h4-12H2,1-3H3
InChI key
TUQOTMZNTHZOKS-UHFFFAOYSA-N
Application
TBP is an uncharged reducing agent for disulfide bonds of cysteine residues. This reagent is ideally suited for preparation of protein samples prior to IEF and 2D electrophoresis. Reduction with TBP and subsequent alkylation with iodoacetamide improves resolution, allows greater sample loads, and therefore, improves visualization of low abundance proteins
Packaging
Sealed ampule of 0.5 mL
signalword
Danger
hcodes
Hazard Classifications
Aquatic Chronic 3 - Eye Dam. 1 - Repr. 1B - Skin Corr. 1A - STOT SE 3
target_organs
Respiratory system
Classe de stockage
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
flash_point_f
186.8 °F - closed cup
flash_point_c
86 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
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Stuart Thomson et al.
Clinical & experimental metastasis, 25(8), 843-854 (2008-08-13)
NSCLC cells with a mesenchymal phenotype have shown a marked reduction in sensitivity to EGFR inhibitors, though the molecular rationale has remained obscure. Here we find that in mesenchymal-like tumor cells both tyrosine phosphorylation of EGFR, ErbB2, and ErbB3 signaling
Tien Q Pham et al.
The Journal of organic chemistry, 70(16), 6369-6377 (2005-07-30)
The phosphine-catalyzed [3 + 2]-cycloaddition of 5-methylenehydantoins 4 with the ylides 5, derived from addition of tributylphosphine to the 2-butynoic acid derivatives, 6a-d, gives spiro-heterocyclic products. The camphor sultam derivative 6b gives optically active products. Noteable was that the ylides
T Oe et al.
Journal of chromatography. B, Biomedical sciences and applications, 708(1-2), 285-289 (1998-07-08)
A method was developed for the simultaneous determination of gamma-glutamylglutathione (gamma-GluGSH) and other low-molecular-mass thiol compounds (cysteine, cysteamine, homocysteine, cysteinylglycine, gamma-glutamylcysteine, glutathione and N-acetylcysteine) using high-performance liquid chromatography combined with precolumn fluorescence labeling with ammonium 7-fluorobenzo-2-oxa-1,3-diazole-4-sulphonate (SBD-F). These SBD-labeled thiol
Numéro d'article de commerce international
| Référence | GTIN |
|---|---|
| T7567-1VL | 04061823927284 |
| T7567-10VL | 04061837378430 |
| T7567-5VL | 04061833298305 |