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76437

Sigma-Aldrich

Pentaethylene glycol monododecyl ether

BioXtra, ≥98.0% (GC)

Synonym(s):

C12E5, Dodecyl pentaethylene glycol ether, Dodecylpentaglycol, Polyoxyethylene (5) lauryl ether

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About This Item

Linear Formula:
CH3(CH2)11(OCH2CH2)5OH
CAS Number:
Molecular Weight:
406.60
Beilstein/REAXYS Number:
1797921
EC Number:
MDL number:
UNSPSC Code:
12161900
PubChem Substance ID:
NACRES:
NA.25

description

non-ionic

Quality Level

product line

BioXtra

assay

≥98.0% (GC)

form

semisolid

mol wt

406.60 g/mol

technique(s)

drug transporter assay: suitable

density

0.963 g/mL at 20 °C (lit.)

cation traces

Ca: ≤50 mg/kg
Cd: ≤50 mg/kg
Co: ≤50 mg/kg
Cr: ≤50 mg/kg
Cu: ≤50 mg/kg
Fe: ≤50 mg/kg
K: ≤50 mg/kg
Mg: ≤50 mg/kg
Mn: ≤50 mg/kg
Na: ≤50 mg/kg
Ni: ≤50 mg/kg
Pb: ≤50 mg/kg
Zn: ≤50 mg/kg

SMILES string

CCCCCCCCCCCCOCCOCCOCCOCCOCCO

InChI

1S/C22H46O6/c1-2-3-4-5-6-7-8-9-10-11-13-24-15-17-26-19-21-28-22-20-27-18-16-25-14-12-23/h23H,2-22H2,1H3

InChI key

LAPRIVJANDLWOK-UHFFFAOYSA-N

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Application

<ul>
<li><strong>Coadsorption of a Monoclonal Antibody and Nonionic Surfactant at the SiO(2)/Water Interface:</strong> This study demonstrates the coadsorption properties of Pentaethylene glycol monododecyl ether with monoclonal antibodies, offering significant implications for biopharmaceutical formulations to improve drug stability and delivery (Lu et al., 2018).</li>
<li><strong>Water-Resistant Surface Modification of Hydrophobic Polymers with Water-Soluble Surfactant Additives:</strong> This research showcases the effectiveness of Pentaethylene glycol monododecyl ether in modifying hydrophobic polymer surfaces to make them water-resistant, pointing to its utility in various industrial and coating applications (Thompson et al., 2021).</li>
<li><strong>Synergistic Role of Temperature and Salinity in Aggregation of Nonionic Surfactant-Coated Silica Nanoparticles:</strong> Highlights the use of Pentaethylene glycol monododecyl ether in nanoparticle stabilization, particularly under varying thermal and saline conditions, beneficial for tailored drug delivery systems and environmental applications (Bharti et al., 2023).</li>
</ul>

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pictograms

CorrosionExclamation mark

signalword

Danger

Hazard Classifications

Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk_germany

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


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Drew R Tietz et al.
Scientific reports, 7(1), 13581-13581 (2017-10-21)
Cytochrome P450 monooxygenases CYP101A1 and MycG catalyze regio- and stereospecific oxidations of their respective substrates, d-camphor and mycinamicin IV. Despite the low sequence homology between the two enzymes (29% identity) and differences in size and hydrophobicity of their substrates, the
D Sato et al.
The Journal of membrane biology, 196(1), 33-39 (2004-01-16)
At 0 to 20 degrees C, the Ca(2+)-ATPase activity of the scallop sarcoplasmic reticulum (SR) was observed to be 7-60% of the peak activity at 30 degrees C, while the ATPase activity of the rabbit SR was 0-7% of its
Anna Bodin et al.
Chemical research in toxicology, 16(5), 575-582 (2003-05-21)
Ethoxylated alcohols, widely used as surfactants, are known to be susceptible to oxidation when exposed to air. At autoxidation, a complex mixture is formed, in which alkyl poly(ethylene glycol) aldehydes, alkyl poly(ethylene glycol) formates, hydroxyaldehydes, and formaldehyde have previously been
Maria Velinova et al.
Langmuir : the ACS journal of surfaces and colloids, 27(23), 14071-14077 (2011-10-11)
Control of the size and agglomeration of micellar systems is important for pharmaceutical applications such as drug delivery. Although shape-related transitions in surfactant solutions are studied experimentally, their molecular mechanisms are still not well understood. In this study, we use
Tiago Mendes Ferreira et al.
Physical chemistry chemical physics : PCCP, 10(39), 6033-6038 (2008-10-01)
A lyotropic nonionic lamellar system composed of pentaethyleneglycol mono n-dodecyl ether and D(2)O was studied using natural abundance (13)C NMR under magic-angle spinning. Applying a two-dimensional recoupling method proposed by Dvinskikh (R-PDLF), (1)H-(13)C dipolar couplings were estimated over a range

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