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282103

Sigma-Aldrich

Triton X-100 reduced

Sinônimo(s):

Polyoxyethylene (10) isooctylcyclohexyl ether

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5 G
R$ 1.088,00
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About This Item

Fórmula linear:
4-(C8H17)C6H10(OCH2CH2)nOH, n~10
Número CAS:
Número MDL:
Código UNSPSC:
12162002
NACRES:
NA.23

R$ 1.088,00


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Nível de qualidade

índice de refração

n20/D 1.473 (lit.)

densidade

1.029 g/mL at 25 °C (lit.)

cadeia de caracteres SMILES

CC(C)(C)CC(C)(C)C1CCC(CC1)OCCOCCOCCOCCOCCOCCOCCO

InChI

1S/C28H56O8/c1-27(2,3)24-28(4,5)25-6-8-26(9-7-25)36-23-22-35-21-20-34-19-18-33-17-16-32-15-14-31-13-12-30-11-10-29/h25-26,29H,6-24H2,1-5H3

chave InChI

QQJNBKDKLMCALZ-UHFFFAOYSA-N

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Descrição geral

Triton X-100 reduced (RTX-100) is formed when the benzene moiety of TX-100 is fully hydrogenated to a cyclohexane derivative. RTX-100 might enhance enzyme digestion and is also known to exhibit some effects on the photoisomerization of bacteriorhodopsin.[1]
Triton X-100 reduced is a versatile nonionic surfactant with a hydrophilic polyethylene oxide chain, widely utilized as a laboratory detergent. Its applications span various areas, including cell biology and biochemical research. This detergent is commonly employed for tasks such as cell lysis to extract proteins or organelles, permeabilizing the membranes of living cells, and serving as a crucial component in lysis buffers. Triton X-100 plays a key role in the isolation of lipid rafts, contributing to enhanced solubility and dispersibility of substances. With a reduced polyoxyethylene content of approximately 10, Triton X-100 exhibits excellent wetting properties and facilitates emulsification.

In biochemical and cell biology research, Triton X-100 is instrumental in solubilizing membrane-bound proteins and isolating lipid rafts. Its unique properties allow for the preservation of the native conformation of proteins obtained from cellular membranes in solution. Triton X-100 reduced is derived from the full hydrogenation of the benzene moiety of TX-100 to a cyclohexane derivative. This modified version, RTX-100, has demonstrated potential in enhancing enzyme digestion and influencing the photoisomerization of bacteriorhodopsin, showcasing its versatility and utility in advanced research applications.

Aplicação

Triton X-100 reduced has been used:
  • as a component of LB-TT for the extraction of total protein from rat brains[2]
  • in ADP-Glo assay and Cytophos adenosine triphosphatase (ATPase) assay[3]
  • in phosphate-buffered saline (PBS) solution for the permeabilization of fibroblasts in 5′ ethynyl uridine staining, immunofluorescence, and immunolabeling[4]

Características e benefícios

  • Non-ionic surfactant
  • Reduced polyoxyethylene content (~10)
  • Improves solubility and dispersibility of substances
  • Excellent wetting properties
  • Enhances emulsification
  • High purity product for research applications

Outras notas

For additional information on our range of Biochemicals, please complete this form.

Informações legais

Triton is a trademark of The Dow Chemical Company or an affiliated company of Dow

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Palavra indicadora

Warning

Frases de perigo

Classificações de perigo

Aquatic Chronic 2 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Órgãos-alvo

Respiratory system

Código de classe de armazenamento

10 - Combustible liquids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

235.4 °F - closed cup

Ponto de fulgor (°C)

113 °C - closed cup

Equipamento de proteção individual

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


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J Fernandez et al.
Analytical biochemistry, 218(1), 112-117 (1994-04-01)
An improved and simplified procedure for enzymatic digestion of proteins bound to polyvinylidene difluoride (PVDF) membranes for obtaining internal protein sequence data is presented. This improved procedure is compatible with various enzymes (trypsin, endoproteinase Lys-C, endoproteinase Glu-C, and clostripain) and
S J Milder et al.
Biochemistry, 30(7), 1751-1761 (1991-02-19)
Time-resolved difference spectra have been obtained for the photocycle of delipidated bacteriorhodopsin monomers (d-BR) in six different detergent micelle environments that were prepared by two new detergent-exchange techniques. A global kinetic analysis of the photocycle spectra for d-BR in each
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