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1-Octadecanaminium, N,N-dimethyl-N-[6-[[12-[(2-methyl-1-oxo-2-propenyl)oxy]-1-oxododecyl] oxy]hexyl]-, bromide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

87279-14-9

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87279-14-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87279-14-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,2,7 and 9 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 87279-14:
(7*8)+(6*7)+(5*2)+(4*7)+(3*9)+(2*1)+(1*4)=169
169 % 10 = 9
So 87279-14-9 is a valid CAS Registry Number.

87279-14-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Dimethyl-{6-[12-(2-methyl-acryloyloxy)-dodecanoyloxy]-hexyl}-octadecyl-ammonium; bromide

1.2 Other means of identification

Product number -
Other names -

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:87279-14-9 SDS

87279-14-9Downstream Products

87279-14-9Relevant academic research and scientific papers

Permeability Characteristics of Polymeric Bilayer Membranes from Methacryloyl and Butadiene Lipids

Dorn, K.,Klingbiel, R. T.,Specht, D. P.,Tyminski, P. N.,Ringsdorf, H.,O'Brien, D. F.

, p. 1627 - 1633 (2007/10/02)

Four polymerizable lipids were synthesized and used for the formation of synthetic bilayer membranes (vesicles).Two of the lipids were methacryloyl ammonium lipids, one with a methacrylamide at the hydrophilic head group of the lipid (α-MA) and one with a methacrylate group at the hydrophobic tail of the lipid (ω-MA).Thermally initiated polymerization of the monomeric bilayer vesicles gave polymers with retention of vesicles structure.The size distribution of the aqueous suspension was not altered significantly on polymerization, and the membranes continued to entrap glucose.The permeability of poly(α-MA) and poly(ω-MA) membranes is about half that of the unpolymerized bilayers.Previously we reported that about 500 monomer units were found per average polymer chain of poly(α-MA) and poly(ω-MA), which shows that there are several (20 to 100) polymer chains per vesicle (Dorn, K. et al.Makromol.Chem., Rapid Commun. 1983, 4, 513).Two butadiene lipids, one based on a phosphatidylcholine (PC) structure, and one with a taurine head group, also formed bilayer membranes, which could be photopolymerized by exposure to ultraviolet light.These lipids have a sorbate unit (λmax 257 nm) in each of the two hydrocarbon chains, which allows the photopolymerization to proceed with the formation of cross-links.Poly(butadiene PC) membranes effectively entrapped glucose for at least a week and were not disrupted by the use of the surfactant Triton X-100.

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