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MilliporeSigma

16758

Poly(éthylene glycol)-blocage-poly(propylène glycol)-blocage-poly(éthylene glycol)

purified, non-ionic

Synonyme(s) :

Poly(ethylene glycol)-block-poly(propylene glycol)-block-poly(ethylene glycol)

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A propos de cet article

Numéro CAS:
UNSPSC Code:
12352104
NACRES:
NA.25
MDL number:
Service technique
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Quality Level

form

powder

quality

purified

impurities

≤1.0% water

pH

5.0-7.5

solubility

soluble, clear, colorless

cation traces

Al: ≤5 mg/kg, As: ≤0.05 mg/kg, Ba: ≤5 mg/kg, Bi: ≤5 mg/kg, Ca: ≤50 mg/kg, Cd: ≤5 mg/kg, Co: ≤5 mg/kg, Cr: ≤5 mg/kg, Cu: ≤5 mg/kg, Fe: ≤5 mg/kg, K: ≤1000 mg/kg, Li: ≤5 mg/kg, Mg: ≤5 mg/kg, Mn: ≤5 mg/kg, Mo: ≤5 mg/kg, Na: ≤50 mg/kg, Ni: ≤5 mg/kg, Pb: ≤5 mg/kg, Sr: ≤5 mg/kg, Zn: ≤5 mg/kg

UV absorption

λ: 260 nm Amax: ≤0.3, λ: 280 nm Amax: ≤0..2

suitability

no residue for filter test

storage temp.

2-8°C

SMILES string

O2C(C2)C.O1CC1

InChI

1S/C3H6O.C2H4O/c1-3-2-4-3;1-2-3-1/h3H,2H2,1H3;1-2H2

InChI key

RVGRUAULSDPKGF-UHFFFAOYSA-N

General description

Poloxamer 407 is a water-soluble, non-ionic surfactant with low toxicity and good solubilizing capacity. This triblock copolymer is composed of a hydrophobic residue of polyoxypropylene (POP) flanked by two hydrophilic units of polyoxyethylene (POE).

Application

Poloxamer 407 has been used:
  • as an inhibitor of lipoprotein lipase activity to assess hepatic very-low-density lipoprotein (VLDL)- triglyceride (TG) secretion in mice
  • for VLDL secretion assay in mice
  • to intraperitoneally inject the mice by dissolving in phosphate buffer saline (PBS) for hepatic triglyceride production

Biochem/physiol Actions

Poloxamer 407 (P407) exhibits reversible gelation properties above a particular polymer concentration and temperature. Poloxamer 407-based sterile injectable formulations serve to be a good candidate for drug delivery. P407 thermo-responsive hydrogels are broadly used as mucosal drug delivery systems as they do not irritate the mucosal membranes. P407 is called an “inactive ingredient” by the U.S. Food and Drug Administration (FDA) for several drug products like oral solutions, suspensions, and inhalation formulations.


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Classe de stockage

11 - Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)



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Nae-Gyune Rim et al.
ACS biomaterials science & engineering, 3(8), 1542-1556 (2017-10-03)
Silk is a promising material for biomedical applications, and much research is focused on how application-specific, mechanical properties of silk can be designed synthetically through proper amino acid sequences and processing parameters. This protocol describes an iterative process between research
Camila S Freitas et al.
Parasitology research, 120(1), 321-335 (2020-11-17)
Treatment for visceral leishmaniasis (VL) is hampered mainly by drug toxicity, their high cost, and parasite resistance. Drug development is a long and pricey process, and therefore, drug repositioning may be an alternative worth pursuing. Cardenolides are used to treat
Hua Qing et al.
Cell, 182(2), 372-387 (2020-07-02)
Acute psychological stress has long been known to decrease host fitness to inflammation in a wide variety of diseases, but how this occurs is incompletely understood. Using mouse models, we show that interleukin-6 (IL-6) is the dominant cytokine inducible upon



Numéro d'article de commerce international

RéférenceGTIN
I6758-10G04061835367061
I6758-1G04061835367078
I6758-5G04061835367085
420290-5GM04055977210828
420291-100GM04055977210859
420291-1GM04055977210835
420291-1KG04055977210842
420291-250GM04055977210873
420291-25GM04055977210866
420291-5GM07790788050108
420322-10GM07790788055622
420322-1KG04055977210569
420322-500GM07790788050153
420322-100GM07790788050146
420322-110GM04055977210590
420322-1GM04055977210552
420322-25GM07790788057817
420322-3.5KG04055977210613
420322-5GM04055977210620
420322-85GM04055977210644
70527-307790788052690
70527-500ML04054839556845