Glycolic acid ethoxylate lauryl ether

Product Information

Molecular Formula:
C43H94O8
Molecular Weight:
739.2
Description
Surfactant. Stabilizer for microemulsions.
Synonyms
dodecan-1-ol,ethane-1,2-diol,2-hydroxyacetic acid,tetradecan-1-ol,tridecan-1-ol; Laureth-4 carboxylic acid; Laureth-6 carboxylic acid; Laureth-11 carboxylic acid
IUPAC Name
2-(2-ethoxyethoxy)acetic acid
Canonical SMILES
OCCO.OCC(O)=O.CCCCCCCCCCCCO.CCCCCCCCCCCCCO.CCCCCCCCCCCCCCO
InChI
InChI=1S/C6H12O4/c1-2-9-3-4-10-5-6(7)8/h2-5H2,1H3,(H,7,8)
InChI Key
LVLQKFRSMSHJIE-UHFFFAOYSA-N
Flash Point
>235.4 °F
Density
1 g/mL at 25 °C
Appearance
Powder
Application
Anionic surfactant.
Refractive Index
1.45

Safety Information

Precautionary Statement
P264, P264+P265, P273, P280, P302+P352, P305+P354+P338, P317, P321, P332+P317, P362+P364, P391, and P501
Signal Word
Danger

Computed Properties

XLogP3
-0.1
Hydrogen Bond Donor Count
1
Hydrogen Bond Acceptor Count
4
Rotatable Bond Count
6
Exact Mass
148.07355886 g/mol
Monoisotopic Mass
148.07355886 g/mol
Topological Polar Surface Area
55.8Ų
Heavy Atom Count
10
Formal Charge
0
Complexity
91.7
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
1
Compound Is Canonicalized
Yes

Patents

Publication Number Title Priority Date
WO-2021254979-A1 Chemokine-selective cxcr4 ectodomain-derived (poly)peptide 2020-06-16
WO-2021221084-A1 Blocked isocyanate composition, heat-curable resin composition, cured product, production method therefor, amidate compound, and catalyst for dissociation of blocking agent for blocked isocyanates 2020-04-30
WO-2021221090-A1 Blocked polyisocyanate composition, heat-curable resin composition, cured product, and production method therefor 2020-04-30
WO-2021200783-A1 Amidate compound, production method therefor, blocking-agent dissociation catalyst, and thermally curable resin composition 2020-03-30
WO-2021177267-A1 Prevention or treatment of aneurysms using mir-33b inhibitor 2020-03-02
WO-2021157587-A1 Method for producing carboxylate compound and method for producing amidate compound 2020-02-03
TW-202136217-A Method for producing carboxylate compound and method for producing amide salt compound 2020-02-03
US-2021238472-A1 Methods for clay swelling inhibition using gemini surfactants containing a saturated linker 2020-01-30
US-2021222052-A1 Gemini surfactants containing an arylene linker for clay swelling inhibition 2020-01-21
US-2021189222-A1 Gemini surfactants containing an unsaturated linker for clay swelling inhibition 2019-12-18

Literatures

PMID Publication Date Title Journal
21705463 2012-01-01 Urinary biomarkers of exposure to glycol ethers and chlorinated solvents during pregnancy: determinants of exposure and comparison with indirect methods of exposure assessment Occupational and environmental medicine
20812373 2011-01-01 Peptide vaccine candidates against classical swine fever virus: T cell and neutralizing antibody responses of dendrimers displaying E2 and NS2-3 epitopes Journal of peptide science : an official publication of the European Peptide Society
15705492 2005-03-28 Biomonitoring of 2-(2-alkoxyethoxy)ethanols by analysing urinary 2-(2-alkoxyethoxy)acetic acids Toxicology letters
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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