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Merck
CN

76437

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:
3055-95-6
Molecular Weight:
406.60
UNSPSC Code:
12161900
NACRES:
NA.25
PubChem Substance ID:
57652637
EC Number:
221-281-8
Beilstein/REAXYS Number:
1797921
MDL number:
MFCD00043064

Key Documents

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InChI key

LAPRIVJANDLWOK-UHFFFAOYSA-N

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

SMILES string

CCCCCCCCCCCCOCCOCCOCCOCCOCCO

description

non-ionic

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

Quality Level

100

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Related Categories

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>

pictograms

CorrosionExclamation mark
GHS05,GHS07

signalword

Danger

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
BCCJ8328
BCCG3187
BCBW6635
BCBR1720V
BCBN3596V

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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
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
H Pfeiffer et al.
Chemistry and physics of lipids, 139(1), 54-67 (2005-11-19)
The present paper reports on the phase behaviour of the pseudobinary aqueous mixtures of 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC)/pentaethylene glycol monododecyl ether (C12E5) and 1,2-dimyristoyl-sn-glycero-3-phosphocholine monohydrate (DMPC)/C12E5. Both systems exhibit a variety of mesophases, such as lamellar gel, liquid crystalline and micellar phases.
Su Yong Kwon et al.
Physical review letters, 89(25), 258302-258302 (2002-12-18)
We have studied the topological transition of the nonionic micelles of a penta-ethyleneglycol mono n-dodecyl ether (C12E5)/DL-alpha-phosphatidylcholine Dimyristoyl (DMPC) mixture in water by light scattering and viscosity measurements. The topological transition concentration decreases with an increase of the mixing ratio
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
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