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

21469-16-9

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21469-16-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 21469-16-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,4,6 and 9 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 21469-16:
(7*2)+(6*1)+(5*4)+(4*6)+(3*9)+(2*1)+(1*6)=99
99 % 10 = 9
So 21469-16-9 is a valid CAS Registry Number.
InChI:InChI=1/C24H38N2O/c1-2-3-4-5-6-7-8-9-10-11-12-17-24(27)25-19-18-21-20-26-23-16-14-13-15-22(21)23/h13-16,20,26H,2-12,17-19H2,1H3,(H,25,27)

21469-16-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[2-(1H-indol-3-yl)ethyl]tetradecanamide

1.2 Other means of identification

Product number -
Other names Myristoyl tryptamine

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:21469-16-9 SDS

21469-16-9Downstream Products

21469-16-9Relevant academic research and scientific papers

Fatty acid-indole fluorescent derivatives as probes to measure the polarity of interfaces containing gangliosides

Bagatolli, Luis A.,Montich, Guillermo G.,Ravera, Mario,Perez, Jorge D.,Fidelio, Gerardo D.

, p. 193 - 202 (2007/10/03)

The fluorescence emission properties of three indole derivative probes N-2-(3-indolyl)ethyl-tetradecanoyl carboxamide (N-myrTAM), 2-tetradecanoyl carboxamidyl-3-(3-indolyl)propanoic acid (N-myrTRP) and 11-N(2-[3-indolyl]ethylamino)-9-en-methyloxy carbonyldecenate (11-TAMundec) were studied in solvents of different polarities in pure lysophosphatidylcholine micelles (lysoPC) and in total brain gangliosides (TBG) micelles using steady-state and phase-modulation fluorometry. By comparing the fluorescence emission spectra in solvent mixtures with the spectra in lipid micelles it is concluded that the probes detect a more polar environment in TBG compared to lysoPC micelles. Quenching experiments with acrylamide indicate that the indole group of N-myrTRP and N-myrTAM are more exposed to the aqueous medium than the indole group of 11-TAMundec both in lysoPC and TBG micelles. Quenching of the indole fluorescence with brominated fatty acid at the position 9-10 of the acyl chain is in the following order: 11-TAMundec > N-MyrTAM > N-MyrTRP in lysoPC micelles whereas in TBG micelles only 11-TAMundec fluorescence is quenched. Based on the results of accessibility of the probes to the aqueous quencher and the dielectric constant calculated for their environment, we estimated the surface to core polarity gradient of the micelles. The polarity gradient is higher in TBG micelles compared to lysoPC micelles.

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