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18451-85-9

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18451-85-9 Usage

General Description

Hexadecanedioic acid 1-methyl ester is a chemical compound primarily identified as an ester derivative of hexadecanedioic acid. This substance is known for its vital role in various scientific research and studies due to its intricate chemical structure and properties. Despite its chemical complexities, it is generally considered safe for handling and usage. However, like most chemicals, protective measures and caution are advised to minimize potential exposure and risks. It exhibits varied characteristics and reactivity based on different conditions and can be manipulated or combined with other compounds for a wide array of chemical reactions, making it a versatile tool in different fields of chemistry and biochemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 18451-85-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,4,5 and 1 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 18451-85:
(7*1)+(6*8)+(5*4)+(4*5)+(3*1)+(2*8)+(1*5)=119
119 % 10 = 9
So 18451-85-9 is a valid CAS Registry Number.

18451-85-9SDS

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 15-(methoxycarbonyl)pentadecanoic acid

1.2 Other means of identification

Product number -
Other names hexadecanedioic acid monomethyl ester

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:18451-85-9 SDS

18451-85-9Relevant articles and documents

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Adams,K.R.,Bonnett,R.

, p. 1885 - 1890 (1971)

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LIPID-MODIFIED NUCLEIC ACID COMPOUNDS AND METHODS

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Paragraph 0550; 0555; 0563, (2019/12/25)

Disclosed herein, inter alia, are lipid-modified nucleic acid compounds of the following structure, their preparation, and their use: (I).

NMR-based molecular ruler for determining the depth of intercalants within the lipid bilayer. Part III: Studies on keto esters and acids

Afri, Michal,Alexenberg, Carmit,Aped, Pinchas,Bodner, Efrat,Cohen, Sarit,Ejgenburg, Michal,Eliyahu, Shlomi,Gilinsky-Sharon, Pessia,Harel, Yifat,Naqqash, Miriam E.,Porat, Hani,Ranz, Ayala,Frimer, Aryeh A.

, p. 105 - 118 (2015/02/19)

The development of "molecular rulers" would allow one to quantitatively locate the penetration depth of intercalants within lipid bilayers. To this end, an attempt was made to correlate the 13C NMR chemical shift of polarizable "reporter" carbons (e.g., carbonyls) of intercalants within DMPC liposomal bilayers - with the polarity it experiences, and with its Angstrom distance from the interface. This requires families of molecules with two "reporter carbons" separated by a known distance, residing at various depths/polarities within the bilayer. For this purpose, two homologous series of dicarbonyl compounds, methyl n-oxooctadecanoates and the corresponding n-oxooctadecanoic acids (n = 4-16), were synthesized. To assist in assignment and detection several homologs in each system were prepared 13C-enriched in both carbonyls. Within each family, the number of carbons and functional groups remains the same, with the only difference being the location of the second ketone carbonyl along the fatty acid chain. Surprisingly, the head groups within each family are not anchored near the lipid-water interface, nor are they even all located at the same depth. Nevertheless, using an iterative best fit analysis of the data points enables one to obtain an exponential curve. The latter gives substantial insight into the correlation between polarity (measured in terms of the Reichardt polarity parameter, ET(30)) and penetration depth into the liposomal bilayer. Still missing from this curve are data points in the moderate polarity range.

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