T7567
Tributylphosphine solution
200 mM (in N-methyl-2-pyrrolidinone), liquid
Synonym(s):
TBP
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About This Item
Empirical Formula (Hill Notation):
C12H27P
CAS Number:
Molecular Weight:
202.32
MDL number:
UNSPSC Code:
41105323
PubChem Substance ID:
NACRES:
NA.56
form
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
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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
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Aquatic Chronic 3 - Eye Dam. 1 - Repr. 1B - Skin Corr. 1A - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 2
Flash Point(F)
186.8 °F - closed cup
Flash Point(C)
86 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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
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
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
Claudia Cattoglio et al.
Proceedings of the National Academy of Sciences of the United States of America, 112(18), E2317-E2326 (2015-04-23)
The embryonic stem cell (ESC) state is transcriptionally controlled by OCT4, SOX2, and NANOG with cofactors, chromatin regulators, noncoding RNAs, and other effectors of signaling pathways. Uncovering components of these regulatory circuits and their interplay provides the knowledge base to
Russell J H Ryan et al.
Cancer discovery, 5(10), 1058-1071 (2015-08-01)
B-cell lymphomas frequently contain genomic rearrangements that lead to oncogene activation by heterologous distal regulatory elements. We used a novel approach called "pinpointing enhancer-associated rearrangements by chromatin immunoprecipitation," or PEAR-ChIP, to simultaneously map enhancer activity and proximal rearrangements in lymphoma
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