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Didecyldimethylammonium bromide, also known as DDAB, is an off-white powder and chunks that is a cationic surfactant with two long alkyl chains. It is soluble in water and organic solvents and has a high charge density, making it a versatile compound for various applications.

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  • 2390-68-3 Structure
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    1. Product Name: Didecyldimethylammonium bromide
    2. Synonyms: DI-N-DECYLDIMETHYLAMMONIUM BROMIDE;DIDECYLDIMETHYLAMMONIUM BROMIDE;didecyl dimethyl Ammonium Bromide 70% solution;Di-n-decyl dimethylammonium bromide, 80% aq. soln.;DDAB-75;DDAB-80;1-Decanaminium, N-decyl-N,N-dimethyl-, bromide;DI-N-DECYLDIMETHYLAMMONIUM BROMIDE: 80% AQUEOUS GEL
    3. CAS NO:2390-68-3
    4. Molecular Formula: Br*C22H48N
    5. Molecular Weight: 406.53
    6. EINECS: 219-234-1
    7. Product Categories: Ammonium Bromides (Quaternary);Quaternary Ammonium Compounds
    8. Mol File: 2390-68-3.mol
  • Chemical Properties

    1. Melting Point: 149-151 °C(lit.)
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: off-white powder and chunks
    5. Density: N/A
    6. Refractive Index: 1.4570
    7. Storage Temp.: Sealed in dry,Room Temperature
    8. Solubility: Soluble in methanol.
    9. Stability: Stable. Incompatible with strong oxidizing agents.
    10. BRN: 6492993
    11. CAS DataBase Reference: Didecyldimethylammonium bromide(CAS DataBase Reference)
    12. NIST Chemistry Reference: Didecyldimethylammonium bromide(2390-68-3)
    13. EPA Substance Registry System: Didecyldimethylammonium bromide(2390-68-3)
  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: 36/37/38
    3. Safety Statements: 26-45-36/37/39-28
    4. WGK Germany: 3
    5. RTECS:
    6. F: 3-10
    7. HazardClass: N/A
    8. PackingGroup: N/A
    9. Hazardous Substances Data: 2390-68-3(Hazardous Substances Data)

2390-68-3 Usage

Uses

Used in Surfactant Applications:
Didecyldimethylammonium bromide is used as a surfactant for its ability to reduce surface tension and stabilize emulsions and foams. It is commonly used in the formulation of detergents, cleaners, and personal care products due to its excellent wetting and dispersing properties.
Used in Phase Transfer Catalysis:
Didecyldimethylammonium bromide is used as a phase transfer catalyst to facilitate the transfer of reactants between immiscible phases, such as between an aqueous and organic phase. This property makes it useful in organic synthesis and industrial processes, where efficient mixing and reaction are required.
Used in Ionic Liquids Preparation:
Didecyldimethylammonium bromide is used in the preparation of hydrophobic ammonium-based ionic liquids. These ionic liquids have unique properties, such as low melting points, high thermal stability, and excellent solvation capabilities, making them suitable for applications in catalysis, electrochemistry, and energy storage.
Used in Nanotechnology:
Didecyldimethylammonium bromide can be used in the synthesis of nanoparticles and the formation of self-assembled monolayers on various substrates. Its ability to form stable colloidal dispersions and control the size and shape of nanoparticles makes it a valuable component in nanotechnology research and applications.
Used in Biomedical Applications:
Didecyldimethylammonium bromide has potential applications in the biomedical field, such as in drug delivery systems and gene therapy. Its cationic nature allows it to interact with negatively charged biological molecules, enabling targeted delivery and enhanced therapeutic effects.
Used in Textile Industry:
In the textile industry, Didecyldimethylammonium bromide is used as a softening agent, providing a smooth and silky feel to fabrics. It also acts as an antistatic agent, reducing the buildup of static electricity on textiles and improving their overall performance.
Used in Cosmetics and Personal Care:
Didecyldimethylammonium bromide is used in cosmetics and personal care products, such as shampoos, conditioners, and creams, for its emulsifying and conditioning properties. It helps to create stable emulsions and improve the texture and feel of these products.
Used in Agriculture:
In agriculture, Didecyldimethylammonium bromide can be used as an adjuvant in pesticide formulations to enhance the effectiveness of active ingredients. Its surfactant properties help to improve the wetting and spreading of pesticides on plant surfaces, leading to better coverage and control of pests and diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 2390-68-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,9 and 0 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2390-68:
(6*2)+(5*3)+(4*9)+(3*0)+(2*6)+(1*8)=83
83 % 10 = 3
So 2390-68-3 is a valid CAS Registry Number.
InChI:InChI=1S/C22H48N.BrH/c1-5-7-9-11-13-15-17-19-21-23(3,4)22-20-18-16-14-12-10-8-6-2;/h5-22H2,1-4H3;1H/q+1;/p-1

2390-68-3 Well-known Company Product Price

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  • Alfa Aesar

  • (B24832)  Di-n-decyl dimethylammonium bromide, 80% aq. gel   

  • 2390-68-3

  • 100g

  • 248.0CNY

  • Detail
  • Alfa Aesar

  • (B24832)  Di-n-decyl dimethylammonium bromide, 80% aq. gel   

  • 2390-68-3

  • 500g

  • 987.0CNY

  • Detail
  • Aldrich

  • (382310)  Didecyldimethylammoniumbromide  98%

  • 2390-68-3

  • 382310-1G

  • 828.36CNY

  • Detail
  • Aldrich

  • (382310)  Didecyldimethylammoniumbromide  98%

  • 2390-68-3

  • 382310-5G

  • 2,825.55CNY

  • Detail
  • Aldrich

  • (382310)  Didecyldimethylammoniumbromide  98%

  • 2390-68-3

  • 382310-250G

  • 8,558.55CNY

  • Detail

2390-68-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name didecyl(dimethyl)azanium,bromide

1.2 Other means of identification

Product number -
Other names Didecyldimethylammonium Bromide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2390-68-3 SDS

2390-68-3Relevant articles and documents

Fluorescence Quenching in Double-Chained Surfactants. 1. Theory of Quenching in Micelles and Vesicles

Miller, D. D.,Evans, D. F.

, p. 323 - 333 (1989)

The time-resolved fluorescence quenching technique is used to investigate the aggregation behavior of double-chained surfactants.With a new extension of this technique, surfactant solutions consisting of (1) only vesicles, (2) mixtures of vesicles and micelles, or (3) only micelles can be distinguished.When applied to solutions of didodecyldimethylammonium acetate, the microstructure is determined to be composed of mainly small micelles over a wide concentration range (0.001-0.1 M); the contribution of vesicles to the total surfactant inventory is quite small.In studies of double-chained surfactants, the technique is particularly valuable for following the transformation of liquid crystalline dispersions to micellar solutions upon heating or dilution.

Supramolecular assistance between cyclodextrins and didecyldimethylammonium chloride against enveloped viruses: Toward eco-biocidal formulations

Leclercq, Lo?c,Dewilde, Anny,Aubry, Jean-Marie,Nardello-Rataj, Véronique

, p. 273 - 281 (2016/09/07)

Nosocomial infections have emerged as important causes of morbidity and mortality in immunocompromised individuals. In this respect, biocides are widely used in hospitals leading to resistant microorganisms. We show here that cyclodextrins can remarkably boost the virucidal activity of di-n-decyldimethylammonium chloride. These oligosaccharides synergistically work with the biocide affording a noticeable reduction of the active virucide concentration between 40 and 85%. Partial replacement of a significant amount of the biocide by eco- and bio-compatible cyclodextrins whilst maintaining the same activity is of great interest as it allows the reduction of the toxicological drawbacks of classical biocide mixtures.

Acidic three-liquid-phase microemulsion systems based on balanced catalytic surfactant for epoxidation and sulfide oxidation under mild conditions

Fressancourt-Collinet, Marion,Hong, Bing,Leclercq, Loic,Alsters, Paul L.,Aubry, Jean-Marie,Nardello-Rataj, Veronique

supporting information, p. 409 - 420 (2013/05/22)

Didecyldimethylammonium tungstate has been designed as a balanced catalytic surfactant to form acidic three-liquid-phase microemulsion systems at room temperature in the presence of water, a non-chlorinated solvent and dimethyldioctylammonium salts (hydrogen sulfate and dihydrogen phosphate). The triphasic system is efficient for the oxidation of olefins, sulfides and thiophenes under mild conditions. Moreover, the recovery and reusability of the catalyst, the straightforward separation of products and catalysts in two distinct phases as well as the possible use of environmentally friendly solvents such as tert-butyl acetate, make this system particularly attractive for catalytic oxidation reactions involving hydrogen peroxide as the primary oxidant under acidic or neutral conditions.

Modeling of multiple equilibria in the self-aggregation of di- n -decyldimethylammonium chloride/octaethylene glycol monododecyl ether/cyclodextrin ternary systems

Leclercq, Loic,Lubart, Quentin,Aubry, Jean-Marie,Nardello-Rataj, Veronique

, p. 6242 - 6252 (2013/07/27)

The surface tension equations of binary surfactant mixtures (di-n-decyldimethylammonium chloride and octaethylene glycol monododecyl ether) are established by combining the Szyszkowski equation of surfactant solutions, the ideal or nonideal mixing theory, and the phase separation model. For surfactant mixtures, the surface tension at the air-water interface is calculated using nonideal theory due to synergism between the two adsorbed surfactant types. The incorporation of cyclodextrin complexation model to the surface tension equations gives a robust model for the description of the surface tension isotherms of binary, ternary, and more complex systems involving numerous inclusion complexes. The surface tension data obtained experimentally shows excellent agreement with the theoretical model below and above the formation of micelles. The strong synergistic effect observed between the two surfactants is disrupted by the presence of CDs, leading to ideal behavior of ternary systems. Indeed, depending on the nature of the cyclodextrin (i.e., α, β, or γ), which allows a tuning of the cavity size, the binding constants with the surfactants are modified as well as the surface properties due to strong modification of equilibria involved in the ternary mixture.

METHODS OF EXCHANGING ANIONS OF TETRAALKYLAMMONIUM SALTS

-

Page/Page column 6, (2009/04/25)

Methods are provided for producing tetra-C1 -C20 alkyl or aryl-substituted Alkyl quaternary ammonium carbonates and bicarbonates. In methods of this invention, at least a tetra-C-1 -C20 alkyl or aryl-substituted alkyl quaternary ammonium bromide, a metal hydroxide, and a suitable solvent are combined, said metal hydroxide being present in a stoichiometric excess as to the quaternary ammonium bromide

METHOD FOR THE SYNTHESIS OF QUATERNARY AMMONIUM COMPOUNDS AND COMPOSITIONS THEREOF

-

Page/Page column 49-50; 55-59, (2008/06/13)

A novel manufacturing process is described for producing quaternary ammonium compounds having a selected anion, which may be useful in wood preservative formulations. The process involves reacting a trialkylamine with an alkyl bromide to form a quaternary tetraalkylammonium bromide salt, converting the quaternary tetraalkylammonium bromide salt to a quaternary tetraalkylammonium hydroxide salt by using an ion exchange resin, and converting the quaternary tetraalkylammonium hydroxide salt to the quaternary tetraalkylammonium salt of the selected anion.

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