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76437

Sigma-Aldrich

Pentaethylene glycol monododecyl ether

BioXtra, ≥98.0% (GC)

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Synonym(s):
C12E5, Dodecyl pentaethylene glycol ether, Dodecylpentaglycol, Polyoxyethylene (5) lauryl ether
Linear Formula:
CH3(CH2)11(OCH2CH2)5OH
CAS Number:
Molecular Weight:
406.60
Beilstein:
1797921
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.25

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

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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Pentaethylene glycol monododecyl ether BioXtra, ≥98.0% (GC)

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Pentaethylene glycol monodecyl ether BioXtra, ≥97.0% (GC)

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Hexaethylene glycol monododecyl ether BioXtra, ≥98.0% (TLC)

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52044

Hexaethylene glycol monododecyl ether

Premium Grade
product line

BioXtra

product line

BioXtra

product line

BioXtra

product line

BioXtra

assay

≥98.0% (GC)

assay

≥98.0% (GC)

assay

≥97.0% (GC)

assay

≥98.0% (TLC)

form

semisolid

form

solid

form

liquid

form

solid

mol wt

406.60 g/mol

mol wt

538.75 g/mol

mol wt

378.54 g/mol

mol wt

450.65 g/mol

technique(s)

drug transporter assay: suitable

technique(s)

-

technique(s)

-

technique(s)

-

Pictograms

CorrosionExclamation mark

Signal Word

Danger

Hazard Statements

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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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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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

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