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Dimethyldioctadecylammonium bromide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

3700-67-2

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3700-67-2 Usage

Uses

Used in Pharmaceutical Industry:
Dimethyldioctadecylammonium bromide is used as a component in the study of drug delivery systems, particularly for its interaction with DNA. This application is crucial for understanding the behavior of the compound in the development of new pharmaceutical formulations and drug delivery methods.
Used in Veterinary Medicine:
In the veterinary medicine industry, Dimethyldioctadecylammonium bromide is used as a component in the investigation of new adjuvants for kill vaccines, specifically for bovine viral diarrhea virus (BVDV). Its role in these studies is to enhance the effectiveness of vaccines and improve overall animal health.
Used in Surface Science:
Dimethyldioctadecylammonium bromide is also utilized in surface science research, where it is employed to study the properties of monolayers through techniques such as specular neutron reflection, surface pressure-area isotherms, and Brewster angle microscopy. These studies contribute to the understanding of the compound's behavior at the molecular level and its potential applications in various industries.

Biochem/physiol Actions

18:0 DDAB is a surface-active molecule, used as an adjuvant to induce systemic immune response. It is non-toxic.

Purification Methods

Crystallise the bromide from acetone, then MeOH [Lukac J Am Chem Soc 106 4387 1984]. Also purify it by chromatography on alumina by washing with *C6H6 and eluting with Me2CO, evaporating and crystallising from MeCN [Swain & Kreevoy J Am Chem Soc 77 1126 1955]. [Beilstein 4 IV 829.]

Check Digit Verification of cas no

The CAS Registry Mumber 3700-67-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,0 and 0 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3700-67:
(6*3)+(5*7)+(4*0)+(3*0)+(2*6)+(1*7)=72
72 % 10 = 2
So 3700-67-2 is a valid CAS Registry Number.
InChI:InChI=1/C38H80N.BrH/c1-5-7-9-11-13-15-17-19-21-23-25-27-29-31-33-35-37-39(3,4)38-36-34-32-30-28-26-24-22-20-18-16-14-12-10-8-6-2;/h5-38H2,1-4H3;1H/q+1;/p-1

3700-67-2 Well-known Company Product Price

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  • Sigma

  • (40165)  Dimethyldioctadecylammoniumbromide  ≥98.0% (AT)

  • 3700-67-2

  • 40165-5G

  • 1,294.02CNY

  • Detail
  • Sigma

  • (40165)  Dimethyldioctadecylammoniumbromide  ≥98.0% (AT)

  • 3700-67-2

  • 40165-25G

  • 4,733.82CNY

  • Detail

3700-67-2SDS

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 Dimethyldioctadecylammonium bromide

1.2 Other means of identification

Product number -
Other names Dimethyldi-n-octadecylammonium 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:3700-67-2 SDS

3700-67-2Relevant academic research and scientific papers

Capping with multivalent surfactants for zeolite nanocrystal synthesis

Jo, Changbum,Jung, Jinhwan,Shin, Hye Sun,Kim, Jaeheon,Ryoo, Ryong

, p. 10014 - 10017 (2013)

Multiammonium surfactants exhibited a remarkable capping effect for zeolite synthesis in the forms of nanoparticles, nanorods, and nanosponges in cases where common monovalent surfactants failed. A nanorod-shaped mordenite zeolite synthesized in this manner showed significantly enhanced catalytic lifetimes in acid-catalyzed cumene synthesis reactions.

Multicomponent Diffusion of Distearyldimethylammonium Polyelectrolyte Solutions in the Presence of Salt: Coupled Transport of Sodium Chloride

Thies, Michael,Clancy, Shaun F.,Paradies, Henrich H.

, p. 9881 - 9891 (2007/10/03)

A sensitive conductance method has been used to determine binary and ternary diffusion coefficients of distearyldimethylammonium chloride, bromide, and hydroxide (DSDMACl, DSDMABr, and DSDMAOH) in aqueous solutions in the absence and presence of salt.Experiments were conducted above and below the critical micelle concentration (CMC) at 25 deg C, and the concentration of salt, when present, was 0.015 M NaX (X = Cl, OH, Br).The experiments reveal that diffusion of DSDMA chloride, bromide, and especially hydroxide induces concurrent flow of NaCl, NaBr, and NaOH, respectively.Also diffusion of DSDMAX in the presence of NaCl drives countertransport of DSDMACl or DSDMAOH.At pH 7.5 and an ionic strength of 0.015 M, each mole of diffusing DSDMACl (Nagg = 72, α = 0.15), cotransports 9.0 mol of NaCl.However, coupled flow of NaCl decreases as the solution pH approaches 5.2 and is almost zero at pH 4.5.The corresponding value for diffusing DSDMAOH at pH 7.5 is about 120 mol of NaCl.At pH 6.5 only 10 mol of NaCl are cotransported, and the value is almost zero at pH 5.5.However, at pH 4.5, diffusing DSDMAOH generates a counterflow of NaCl due to bound protons and a release of H2O (DSDMAOH + H(1+) DSDMA(1+) + H2O), yielding a net positive charge; hence, the D21 value is negative.The cross-diffusion coefficient D21 of diffusing DSDMACl in the presence of 0.015 M (0.095-0.009) NaOH and 0.015 M NaCl yields a flux density of NaOH and NaCl, which is generated by the DSDMAX (X = Cl + OH) gradient.A similar cross-diffusion coefficient, D21, is revealed when DSDMAOH, is used, instead of DSDMACl, in the presence of 0.015 M NaCl through induced coupled transport of salt.The coupled transport of NaCl or of NaCl and NaOH is primarily driven by the diffusion-induced electric field along the DSDMAOH and DSDMACl concentration gradients.For the DSDMAOH system, the direction and magnitude of the coupled flow of either NaCl or NaOH can be explained through the ionic mobility of DSDMA(1+) and OH(1-), in addition to the charge and degree of dissociation (Nagg = 6400, α = 0.33-0.35) at 25 deg C.The tracer and mutual diffusion coefficients for the DSDMAX system were compared with those from light-scattering measurements of polyelectrolyte solutions of DSDMAX.

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