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Hexadecanoic acid, 10-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

17001-26-2

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17001-26-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17001-26-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,0,0 and 1 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 17001-26:
(7*1)+(6*7)+(5*0)+(4*0)+(3*1)+(2*2)+(1*6)=62
62 % 10 = 2
So 17001-26-2 is a valid CAS Registry Number.

17001-26-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 10-methylhexadecanoic acid

1.2 Other means of identification

Product number -
Other names 10Me16:0 fatty acid

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:17001-26-2 SDS

17001-26-2Downstream Products

17001-26-2Relevant academic research and scientific papers

Isolation of Five-Membered Cyclitol Glycolipids, Crasserides: Unique Glycerides from the Sponge Pseudoceratina crassa

Constantino, Valeria,Fattorusso, Ernesto,Mangoni, Alfonso

, p. 186 - 191 (1993)

Crasserides 1a-6a, six new glycolipid analogues in which the sugar moiety is replaced by an unprecedented five-membered cyclitol, were isolated as a mixture from the sponge Pseudoceratina crassa (Hyatt), and their structures were determined by spectroscopic and chemical analysis.Compounds 1a-6a showed a high antifeedant activity on the fish Carassius auratus, which suggests their potential role as natural feeding deterrents.

Synthesis of specific deuterated derivatives of the long chained stratum corneum lipids [EOS] and [EOP] and characterization using neutron scattering

Sonnenberger, Stefan,Eichner, Adina,Schmitt, Thomas,Hau?, Thomas,Lange, Stefan,Langner, Andreas,Neubert, Reinhard H.H.,Dobner, Bodo

, p. 316 - 330 (2017/06/08)

The synthesis of specific deuterated derivatives of the long chained ceramides [EOS] and [EOP] is described. The structural differences with respect to the natural compounds are founded in the substitution of the 2 double bonds containing linoleic acid by a palmitic acid branched with a methyl group in 10-position. The specific deuteration is introduced both in the branched and in the terminal methyl group, which was realized by common methods of successive deuteration of carboxylic groups in 3 steps. These modified fatty acids resp. the corresponding ceramides [EOS] and [EOP] were prepared for neutron scattering investigations. First results of these investigations were presented in this manuscript showing that the deuterated compounds could be detected in the stratum corneum lipid model membranes. The deuterated ceramides [EOS] and [EOP] are valuable tools to investigate the influence of these long chained ceramide species on the nanostructure of stratum corneum lipid model membranes.

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