JavaScript seems to be disabled in your browser. For the best experience on our site, be sure to turn on Javascript in your browser.

This is a demo store. No orders will be fulfilled.

Account

Settings

Language

྾

Home
Chemistry & Biochemicals
Catalysts
Organocatalysts
Dodecylethyldimethylammonium bromide - 99%, high purity , CAS No.68207-00-1

Skip to the end of the images gallery

Skip to the beginning of the images gallery

Dodecylethyldimethylammonium bromide - 99%, high purity , CAS No.68207-00-1

2 Citations

COA

Grade & Purity:

≥99%

Cas Number: 68207-00-1
Molecular Weight: 322.37
Beilstein Registry Number: 6007021
EC Number: 269-249-2
MDL number: MFCD00043170
PubChem CID: 9880197

In stock

Item Number

D113032

Grouped product items
SKU	Size	Availability	Price
D113032-5g	5g	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$19.90
D113032-25g	25g	3	$77.90
D113032-100g	100g	2	$223.90

Basic Description

Synonyms	EDDAB \| 1-Dodecanaminium, N-ethyl-N,N-dimethyl-, bromide \| N-Ethyl-N,N-dimethyldodecan-1-aminium bromide \| N-Dodecyl-N,N-dimethyl-N-ethylammonium bromide \| Q27274290 \| DODECYL-N,N-DIMETHYL-N-ETHYLAMMONIUM BROMIDE \| MFCD00043170 \| B2YOU5667H \| DODECYL(ETHY
Specifications & Purity	≥99%
Storage Temp	Room temperature,Desiccated
Shipped In	Normal
Product Description	Application： Dodecylethyldimethylammonium bromide (C12EDMAB) can be used: As a growth-directing surfactant in the synthesis of monodisperse gold nanorods. As a surfactant in the synthesis of poly(methyl methacrylate)-poly(N-isopropylacrylamide) core-shell particles via emulsion polymerization. As an additive in the synthesis of mesoporous nanocrystalline TiO2 microspheres to increasing the degree of crystallization and modification in the texture of TiO2.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organic nitrogen compounds
  - Class Organonitrogen compounds
    - Subclass Quaternary ammonium salts

Kingdom	Organic compounds
Superclass	Organic nitrogen compounds
Class	Organonitrogen compounds
Subclass	Quaternary ammonium salts
Intermediate Tree Nodes	Not available
Direct Parent	Tetraalkylammonium salts
Alternative Parents	Organic bromide salts Hydrocarbon derivatives Amines Organic cations
Molecular Framework	Aliphatic acyclic compounds
Substituents	Tetraalkylammonium salt - Hydrocarbon derivative - Organic bromide salt - Organic salt - Amine - Organic cation - Aliphatic acyclic compound
Description	This compound belongs to the class of organic compounds known as tetraalkylammonium salts. These are organonitrogen compounds containing a quaternary ammonium substituted with four alkyl chains.
External Descriptors	Not available
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Associated Targets(Human)

DNM1 Tbio Dynamin-1 (215 Activities)

Discover Target: DNM1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mechanisms of Action

Mechanism of Action	Action Type	target ID	Target Name	Target Type	Target Organism	Binding Site Name	References

Names and Identifiers

IUPAC Name	dodecyl-ethyl-dimethylazanium;bromide
INCHI	InChI=1S/C16H36N.BrH/c1-5-7-8-9-10-11-12-13-14-15-16-17(3,4)6-2;/h5-16H2,1-4H3;1H/q+1;/p-1
InChIKey	FFGSPQDSOUPWGY-UHFFFAOYSA-M
Smiles	CCCCCCCCCCCC[N+](C)(C)CC.[Br-]
Isomeric SMILES	CCCCCCCCCCCC[N+](C)(C)CC.[Br-]
WGK Germany	3
Molecular Weight	322.37
Beilstein	6007021
Reaxy-Rn	6007021
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=6007021&ln=

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

6 results found

Lot Number	Certificate Type	Date	Item
F2315742	Certificate of Analysis	Mar 04, 2025	D113032
F2315747	Certificate of Analysis	Mar 04, 2025	D113032
J2431667	Certificate of Analysis	Apr 01, 2024	D113032
C2308589	Certificate of Analysis	Mar 24, 2023	D113032
I1515166	Certificate of Analysis	Jan 05, 2023	D113032
K2208100	Certificate of Analysis	Nov 10, 2022	D113032

Chemical and Physical Properties

Sensitivity	Moisture sensitive
Melt Point(°C)	185-188°C
Molecular Weight	322.370 g/mol
XLogP3
Hydrogen Bond Donor Count	0
Hydrogen Bond Acceptor Count	1
Rotatable Bond Count	12
Exact Mass	321.203 Da
Monoisotopic Mass	321.203 Da
Topological Polar Surface Area	0.000 Å²
Heavy Atom Count	18
Formal Charge	0
Complexity	152.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	2

Citations of This Product

How to Cite Aladdin Scientific Products?

1. Haofei Li, Zhuojun Cai, Yilin Wang. (2020) Impact Behaviors on Superhydrophobic Surfaces for Water Droplets of Asymmetric Double-Chain Quaternary Ammonium Surfactants. LANGMUIR, 36 (46): (14113–14122).
2. Jinghui Wang, Renliang Huang, Wei Qi, Rongxin Su, Zhimin He. (2017) Oriented Enzyme Immobilization at the Oil/Water Interface Enhances Catalytic Activity and Recyclability in a Pickering Emulsion. LANGMUIR, 33 (43): (12317–12325).

Solution Calculators

Molarity Calculator

Determine the necessary mass, volume, or concentration for preparing a solution.

Mass

Concentration

Volume

M. Wt*

g/mol

*When preparing stock solutions, always use the batch-specific molecular weight of the product found on the vial label and the Certificate of Analysis (available online).

Dilution Calculator

Determine the dilution needed to prepare a stock solution.

Concentration 1 (C1)

Volume 1 (V1)

Concentration 2 (C2)

Volume 2 (V2)

Reconstitution Calculator

The reconstitution calculator enables you to quickly determine the volume of a reagent needed to reconstitute your vial. Just enter the mass of the reagent and the target concentration, and the calculator will do the rest.

Volume (to add to vial)

Mass (in vial)

Desired Reconstitution Concentration

Reviews

Shall we send you a message when we have discounts available?

Remind me later

Thank you! Please check your email inbox to confirm.

Oops! Notifications are disabled.