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Merck
CN

X305

Triton X-305 solution

70% in H2O

Synonym(s):

Polyethylene glycol mono(4-tert-octylphenyl) ether, Polyethylene glycol p-octylphenol ether

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About This Item

CAS Number:
UNSPSC Code:
12161900
NACRES:
NA.21
MDL number:
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Product Name

Triton X-305 solution, 70% in H2O

SMILES string

O(CCO)c1ccc(cc1)C(CC(C)(C)C)(C)C

InChI

1S/C16H26O2/c1-15(2,3)12-16(4,5)13-6-8-14(9-7-13)18-11-10-17/h6-9,17H,10-12H2,1-5H3

InChI key

JYCQQPHGFMYQCF-UHFFFAOYSA-N

description

non-ionic

mol wt

~1526.0 g/mol

concentration

70% in H2O

technique(s)

blocking: suitable
cell culture | mammalian: suitable
hybridization: suitable
immunohistochemistry: suitable
protein purification: suitable

CMC

0.65 mM

transition temp

cloud point >100 °C

HLB

17.3

Quality Level

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Legal Information

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

Application

Triton X-305 has been used:
  • In the treatment of cells for immunocytochemistry
  • Along with peroxotungstic acid in the preparation of tungsten trioxide films by sol-gel method
  • In the dispersion polymerization of styrene with activated poly(N-vinylpyrrolidone) (PVP) for the synthesis of lanthanide-encoded polystyrene particles

General description

Triton X-305 is a non-ionic surfactant. This octylphenol ethoxylate has higher number of ethylene oxide units, increased cmc (Critical micelle concentration) and hydrophile/lipophile balance when compared to Triton X-100. Triton X-305 is compatible with anionic, cationic, and other nonionic surfactants and chemically stable in most acidic and alkaline solutions.

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Skin Irrit. 2

Storage Class

10 - Combustible liquids

wgk

WGK 2

flash_point_f

483.8 °F - closed cup

flash_point_c

251 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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Solubilization of phospholipid bilayers by surfactants belonging to the Triton X series: Effect of polar group size.
Partearroyo M A, et al.
Journal of Colloid and Interface Science, 178(1), 156-159 (1996)
Controlling particle size and photoelectrochemical properties of nanostructured WO3 with surfactants.
Memar A, et al.
Applied Surface Science, 305, 760-767 (2014)
Surface functionalization methods to enhance bioconjugation in metal-labeled polystyrene particles.
Macromolecules, 44(12), 4801-4813 (2011)
Thangavel Ponrasu et al.
Polymers, 13(2) (2021-01-16)
The fast-dissolving drug delivery systems (FDDDSs) are developed as nanofibers using food-grade water-soluble hydrophilic biopolymers that can disintegrate fast in the oral cavity and deliver drugs. Jelly fig polysaccharide (JFP) and pullulan were blended to prepare fast-dissolving nanofiber by electrospinning.
Hirokazu Yokoyama et al.
Langmuir : the ACS journal of surfaces and colloids, 29(3), 857-860 (2012-12-29)
In this report, we present a novel approach for the elucidation of the physicochemical properties of lipid membranes by isothermal titration calorimetry (ITC) to quantify the heat absorbed during the solubilization of vesicles into TritonX-100 micelles. By using large and

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