Lithium dodecyl sulfate

Product Information

Molecular Formula:
C12H25LiO4S
Molecular Weight:
272.33
Description
Lithium dodecyl sulfate is a versatile compound extensively utilized in the biomedical sector. It showcases remarkable prowess as a surfactant agent. Its paramount significance lies within the realm of drug formulation, predominantly in the efficacious delivery of hydrophobic pharmaceuticals. Moreover, this compound assumes a pivotal role in the progression of analytical approaches for disease identification, exemplified by its profound implication in the identification of cancer-associated biomarkers.
Synonyms
Dodecyl lithium sulfate, Dodecyl sulfate lithium salt, Lauryl sulfate lithium salt, Lithium lauryl sulfate
IUPAC Name
lithiumdodecyl sulfate
Canonical SMILES
[Li+].CCCCCCCCCCCCOS(=O)(=O)[O-]
InChI
InChI=1S/C12H26O4S.Li/c1-2-3-4-5-6-7-8-9-10-11-12-16-17(13,14)15/h2-12H2,1H3,(H,13,14,15)/q+1/p-1
InChI Key
YFVGRULMIQXYNE-UHFFFAOYSA-M
Purity
>98.0%(T)
Appearance
White to Almost white powder to crystal
Application
Used to formulate washing-cleaning products and as a laboratory reagent.

Safety Information

Hazards
H315:
Causes skin irritation.
H319:
Causes serious eye irritation.
Precautionary Statement
P264:
Wash thoroughly after handling.
P280:
Wear protective gloves/protective clothing/eye protection/face protection.
P302+P352:
IF ON SKIN:
Wash with plenty of soap and water.
P332+P313:
If skin irritation occurs:
Get medical advice/attention.
P337+P313:
If eye irritation persists:
Get medical advice/attention.
P362+P364:
Take off contaminated clothing. [As modified by IV ATP].
And wash it before reuse. [Added by IV ATP].

Computed Properties

Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
4
Rotatable Bond Count
12
Exact Mass
272.16335888 g/mol
Monoisotopic Mass
272.16335888 g/mol
Topological Polar Surface Area
74.8Ų
Heavy Atom Count
18
Formal Charge
0
Complexity
249
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
2
Compound Is Canonicalized
Yes

Patents

Publication Number Title Priority Date
CN-114181932-A Nucleic acid releasing agent and its application 2021-12-03
JP-2022017429-A Electrode complexes, batteries, electronic devices 2021-10-29
CN-113991073-A Preparation method of lithium sulfide electrode material 2021-09-27
CN-113528295-A Microfluidic chip capable of carrying out multi-step time sequence reaction, microfluidic method and application thereof 2021-09-10
CN-113528295-B Microfluidic chip capable of carrying out multi-step time sequence reaction, microfluidic method and application thereof 2021-09-10
CN-113667744-A Gene polymorphism detection kit for rocuronium bromide metabolic marker and detection method and application thereof 2021-09-10
CN-113667745-A Gene polymorphism detection kit for drug effect prediction of tumor necrosis factor alpha inhibitor, detection method and application thereof 2021-09-10
CN-113736874-A Gene polymorphism detection kit for salbutamol metabolic marker, detection method and application thereof 2021-09-10
CN-113755579-A Gene polymorphism detection kit for tacrolimus metabolic marker and detection method and application thereof 2021-09-10
CN-113755589-A Gene polymorphism detection kit for platinum drug metabolic markers and detection method and application thereof 2021-09-10

Literatures

PMID Publication Date Title Journal
22614027 2012-07-30 Organo/LDH nanocomposite as an adsorbent of polycyclic aromatic hydrocarbons in water and soil-water systems Journal of hazardous materials
22498503 2012-05-01 Structure and dynamics of β-lactoglobulin in complex with dodecyl sulfate and laurate: a molecular dynamics study Biophysical chemistry
22172289 2012-02-27 Low frequency sonophoresis mediated transdermal and intradermal delivery of ketoprofen International journal of pharmaceutics
22309403 2012-02-01 E. coli o157:H7 population reduction from alfalfa seeds with malic acid and thiamine dilauryl sulfate and quality evaluation of the resulting sprouts Journal of food science
22060013 2011-12-20 Comparative studies on the crystalline to fluid phase transitions of two equimolar cationic/anionic surfactant mixtures containing dodecylsulfonate and dodecylsulfate Langmuir : the ACS journal of surfaces and colloids
22022703 2011-12-14 Integrative and intermediate self-assembly of multi-walled hybrid nanotubes for catanionic biomimetics Chemical communications (Cambridge, England)
21924540 2011-12-01 Interaction of a two-transmembrane-helix peptide with lipid bilayers and dodecyl sulfate micelles Biophysical chemistry
21978582 2011-11-30 Organo/layered double hydroxide nanohybrids used to remove non ionic pesticides Journal of hazardous materials
21939262 2011-11-09 Complexes of native ubiquitin and dodecyl sulfate illustrate the nature of hydrophobic and electrostatic interactions in the binding of proteins and surfactants Journal of the American Chemical Society
21913555 2011-08-01 [Comparison of mtDNA extracting methods for common sarcosaphagous insects] Fa yi xue za zhi
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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