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Structure

Sodium Dodecyl Sulfate

CAS
151-21-3
Catalog Number
ACM151213-3
Category
Main Products
Molecular Weight
288.38
Molecular Formula
C12H25NaO4S

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Specification

Description
Sodium dodecyl sulfate, synonymously sodium lauryl sulfate (or laurilsulfate; SDS or SLS, respectively), is a synthetic organic compound with the formula CH3(CH2)11SO4Na. It is an anionic surfactant used in many cleaning and hygiene products. The sodium salt is of an organosulfate class of organics. It consists of a 12-carbon tail attached to a sulfate group,[not verified in body] i.e., it is the sodium salt of dodecyl hydrogen sulfate, the ester of dodecyl alcohol and sulfuric acid. Its hydrocarbon tail combined with a polar "headgroup" give the compound amphiphilic properties and so make it useful as a detergent.[not verified in body] Also derived as a component of mixtures produced from inexpensive coconut and palm oils, SDS is a common component of many domestic cleaning, personal hygiene and cosmetic, pharmaceutical, and food products, as well as of industrial and commercial cleaning and product formulations.[not verified in body]
Synonyms
Aquarexmethyl
IUPAC Name
Sodium;dodecyl sulfate
Canonical SMILES
CCCCCCCCCCCCOS(=O)(=O)[O-].[Na+]
InChI
InChI=1S/C12H26O4S.Na/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
DBMJMQXJHONAFJ-UHFFFAOYSA-M
Boiling Point
216 °C
Melting Point
204-207 °C(lit.)
Flash Point
>100 °C
Density
1.03 g/mL at 20 °C
Solubility
Soluble in water
Appearance
Powder or crystals
Application
Leather assistant, plastic auxiliaries, biocide
Storage
2-8 °C
Active Content
95.0%
Cloud Point
>100 °C
Complexity
249
Covalently-Bonded Unit Count
2
Defined Atom Stereocenter Count
0
EC Number
205-788-1
Exact Mass
288.13712473
Formal Charge
0
Hazard Codes
F
Hazard Statements
F:Flammable
Heavy Atom Count
18
HS Code
3402110000
Hydrogen Bond Acceptor Count
4
Hydrogen Bond Donor Count
0
Isomeric SMILES
CCCCCCCCCCCCOS(=O)(=O)[O-].[Na+]
LogP
4.46490
MDL Number
MFCD00036175
Monoisotopic Mass
288.13712473
pH
6-9
Physical State
Solid
PSA
74.81
RIDADR
UN 2926
Rotatable Bond Count
12
Safety Description
S26-S36/37/39
Stability
Stable under normal temperatures and pressures.
Storage Conditions
Room temperature
Topological Polar Surface Area
74.8 Ų
WGK Germany
2

Sodium Dodecyl Sulfate's Impact on Human Transferrin Structure and Iron-Binding Dynamics

Sodium dodecyl sulfate rearranges the conformation of transferrin and attenuates its iron-binding capacity Liu M, et al. Science of The Total Environment, 2024, 177159.

Sodium dodecyl sulfate (SDS) demonstrates significant effects on human transferrin (HTF), particularly regarding iron-binding capacity and structural integrity. Recent studies highlight SDS's capacity to bind tightly with HTF at a single binding site, characterized by strong binding constants and spontaneous interaction, as confirmed through isothermal titration calorimetry (ITC) data (ΔG = -40.1 kcal·mol⁻¹). This interaction disrupts the secondary structure of HTF and alters its conformation, leading to a dose-dependent release of bound iron ions.
Spectroscopic analysis further revealed that SDS distorts the microenvironment of aromatic amino acids within HTF, resulting in weakened iron-binding. Molecular docking has identified a distinct dual interaction mechanism: SDS's hydrophobic tail engages HTF through hydrophobic forces, while the hydrophilic head forms hydrogen bonds. These findings, aligned with ITC data, indicate that SDS disrupts HTF's stability and iron-carrying function through a concerted hydrophobic and hydrogen bonding process.

Sodium Dodecyl Sulfate as a Surface Modifier in PVDF-ZFO Composites for Enhanced Energy Storage

Effect of sodium dodecyl sulfate on the dielectric and electrical properties of poly (vinylidene fluoride)-zinc ferrite composites Sethy M, et al. Journal of Molecular Structure, 2025, 1321, 139782.

A polymer composite material with polyvinylidene fluoride (PVDF) as the matrix, zinc ferrite (ZnFe₂O₄, ZFO) as the ceramic filler, and sodium dodecyl sulfate (SDS) as a surface modifier was synthesized via a straightforward solvent-casting method for use in energy storage devices.
Synthesis of Zinc Ferrite (ZnFe₂O₄, ZFO) Nanoparticles
Zinc nitrate (Zn(NO₃)₂·6H₂O) and ferric nitrate (Fe(NO₃)₃·9H₂O) were combined at a molar ratio of 1:2 and dissolved in distilled water. Ethylenediaminetetraacetic acid (EDTA) was then added in molar ratios ranging from 1:1 to 1:5 with respect to the metal nitrates. The solution was mixed for 1 hour at room temperature using a magnetic stirrer. The mixture was heated to approximately 110°C until a black powder formed, which was then calcined at 750°C for 4 hours to obtain the ZFO nanopowder.
Synthesis of PVDF-ZFO-SDS Composite Film
First, PVDF was dissolved in DMF and stirred for 30 minutes. Separately, a designated amount of the synthesized ZFO nanopowder was dispersed in DMF, subjected to 1 hour of ultrasonic treatment to ensure uniform dispersion of the nanoparticles, and stirred for an additional 30 minutes. The PVDF and ZFO-DMF solutions were then combined and stirred for another 30 minutes to achieve a homogeneous solution. SDS was added to ZFO dispersed in DMF at various concentrations and stirred for 1 hour. In a separate flask, a PVDF-DMF mixture was stirred for 1 hour until a uniform, transparent solution formed. Finally, the solution containing SDS and ZFO was added to the PVDF solution. The complete mixture was sonicated and stirred for another 30 minutes before being poured into petri dishes and dried in a hot-air oven for 6 hours to produce the PVDF-ZFO-SDS composite film.

Sodium Dodecyl Sulfate in Protein Removal from Industrial Chitosan

Sodium dodecyl sulfate assisted electric field treatment for deproteinization of chitosan Zhao Z, et al. Colloids and Surfaces A: Physicochemical and Engineering Aspects, 2024, 703, 135187.

Sodium Dodecyl Sulfate (SDS) demonstrates significant promise in biomedical applications, particularly as a surfactant for effective protein removal from industrial-grade chitosan. The study under review explores a novel method utilizing an electric field in an SDS medium to achieve high-efficiency deproteinization of chitosan, producing material with a residual protein content as low as 0.151 wt%.
Using orthogonal experimental design, key parameters were optimized, including electric field intensity, SDS concentration, and electrophoresis duration. This design matrix (L9 (3^4)), with three factors-voltage (100 V, 300 V, 500 V), SDS concentration (0.1 wt%, 0.5 wt%, 1 wt%), and electrophoresis time (0.5 h, 1 h, 2 h)-determined that an optimal condition of 300 V, 1 wt% SDS, and a 2-hour treatment time yielded the highest protein removal efficiency. The efficiency is attributed to the strong electrostatic interaction between SDS molecules and residual proteins. SDS forms complexes with the proteins, imparting a negative charge that enables the migration of the SDS-protein complex under the electric field, thereby effectively separating it from the chitosan matrix.
The study highlights the potential of SDS in facilitating an effective, low-cost, and scalable method for chitosan deproteinization, positioning SDS as an essential reagent in enhancing the biomedical compatibility of industrial chitosan.

What is the molecular weight of Sodium Dodecyl Sulfate?

The molecular weight of Sodium Dodecyl Sulfate is 288.38 g/mol.

What is the role of Sodium Dodecyl Sulfate?

Sodium Dodecyl Sulfate has a role as a detergent and a protein denaturant.

What are some synonyms for Sodium Dodecyl Sulfate?

Some synonyms for Sodium Dodecyl Sulfate include Sodium lauryl sulfate, Sodium dodecylsulfate, and Sodium lauryl sulphate.

What is the IUPAC Name of Sodium Dodecyl Sulfate?

The IUPAC Name of Sodium Dodecyl Sulfate is sodium;dodecyl sulfate.

What is the Canonical SMILES of Sodium Dodecyl Sulfate?

The Canonical SMILES of Sodium Dodecyl Sulfate is CCCCCCCCCCCCOS(=O)(=O)[O-].[Na+].

What is the CAS number for Sodium Dodecyl Sulfate?

The CAS number for Sodium Dodecyl Sulfate is 151-21-3.

How does Sodium Dodecyl Sulfate appear physically?

Sodium Dodecyl Sulfate appears as white to pale yellow paste or liquid with a mild odor.

Where can Sodium Dodecyl Sulfate be used?

Sodium Dodecyl Sulfate is used as a fat emulsifier, wetting agent, and detergent in cosmetics, pharmaceuticals, and toothpastes.

What is the molecular formula of Sodium Dodecyl Sulfate?

The molecular formula of Sodium Dodecyl Sulfate can be NaSO4C12H25, C12H25O4S.Na, or C12H25NaO4S.

What is the role of Sodium Dodecyl Sulfate in protein biochemistry?

Sodium Dodecyl Sulfate is used as a research tool in protein biochemistry.

What is the CAS number of Sodium Dodecyl Sulfate?

The CAS number of Sodium Dodecyl Sulfate is 151-21-3.

Where is Sodium Dodecyl Sulfate used?

Sodium Dodecyl Sulfate is used in cosmetics, pharmaceuticals, toothpastes, and as a research tool in protein biochemistry.

What is the description of Sodium Dodecyl Sulfate according to the U.S. Coast Guard?

Sodium Dodecyl Sulfate appears as a white to pale yellow paste or liquid with a mild odor, and sinks and mixes with water.

What is the parent compound and component compounds of Sodium Dodecyl Sulfate?

The parent compound of Sodium Dodecyl Sulfate is Lauryl sulfate (CID 8778), and the component compounds are Lauryl sulfate (CID 8778) and Sodium (CID 5360545).

Upstream Synthesis Route 1

  • 112-53-8
  • 151-21-3

Reference: [1] Journal of Physical Chemistry, 1991, vol. 95, # 4, p. 1671 - 1676
[2] Journal of Physical Chemistry, 1983, vol. 87, # 7, p. 1264 - 1277
[3] Journal of the Chemical Society, Perkin Transactions 2, 2001, # 9, p. 1489 - 1495
[4] Patent: US4973686, 1990, A,

Upstream Synthesis Route 2

  • 2467-15-4
  • 151-21-3

Reference: [1] Patent: EP2851362, 2015, A1, . Location in patent: Paragraph 0036

Downstream Synthesis Route 1

  • 16110-09-1
  • 151-21-3
  • 109-89-7
  • 1066-54-2
  • 86873-60-1

Reference: [1] Patent: US5380861, 1995, A,

Downstream Synthesis Route 2

  • 1119-94-4
  • 151-21-3
  • 15830-42-9

Reference: [1]Jokela, Paeivi; Joensson, Bengt; Khan, Ali
[Journal of Physical Chemistry, 1987, vol. 91, # 12, p. 3291 - 3298]
[2]Location in patent: experimental part
Huang, Zheng-Lin; Hong, Jhen-Yi; Chang, Chien-Hsiang; Yang, Yu-Min
[Langmuir, 2010, vol. 26, # 4, p. 2374 - 2382]
[3]Location in patent: experimental part
Wu, Fu-Gen; Yu, Ji-Sheng; Sun, Shu-Feng; Yu, Zhi-Wu
[Langmuir, 2011, vol. 27, # 24, p. 14740 - 14747]
[4]Mihelj, Tea; Popović, Jasminka; Skoko, Željko; Tomašić, Vlasta
[Thermochimica Acta, 2014, vol. 591, p. 119 - 129]

* For details of the synthesis route, please refer to the original source to ensure accuracy.

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