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2409-15-6

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2409-15-6 Usage

Physical Appearance

White to off-white solid

Solubility

Insoluble in water, soluble in organic solvents

Industrial Applications

Surfactant
Antistatic agent
Lubricant additive

Use in Cosmetics and Personal Care Products

Emollient
Skin conditioning agent

Pharmaceutical Potential

Treatment of inflammatory and autoimmune diseases

Safety Information

May cause skin and eye irritation, handle with caution.

Check Digit Verification of cas no

The CAS Registry Mumber 2409-15-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,0 and 9 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2409-15:
(6*2)+(5*4)+(4*0)+(3*9)+(2*1)+(1*5)=66
66 % 10 = 6
So 2409-15-6 is a valid CAS Registry Number.
InChI:InChI=1/C17H36N2O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-19-17(18)20/h2-16H2,1H3,(H3,18,19,20)

2409-15-6SDS

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 Hexadecyl-harnstoff

1.2 Other means of identification

Product number -
Other names N-palmitylurea

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:2409-15-6 SDS

2409-15-6Downstream Products

2409-15-6Relevant articles and documents

Hierarchical Self-Assembly of Amphiphilic β-C-Glycosylbarbiturates into Multiresponsive Alginate-Like Supramolecular Hydrogel Fibers and Vesicle Hydrogel

Yao, Shun,Brahmi, Robin,Portier, Fran?ois,Putaux, Jean-Luc,Chen, Jing,Halila, Sami

supporting information, p. 16716 - 16721 (2021/10/19)

Ordered molecular self-assembly of glycoamphiphiles has been regarded as an attractive, practical and bottom-up approach to obtain stable, structurally well-defined, and functional mimics of natural polysaccharides. This study describes a versatile and rational design of carbohydrate-based hydrogelators through N,N’-substituted barbituric acid-mediated Knoevenagel condensation onto unprotected carbohydrates in water. Amphiphilic N-substituted β-C-maltosylbarbiturates self-assembled into pH- and calcium-triggered alginate-like supramolecular hydrogel fibers with a multistimuli responsiveness to temperature, pH and competitive metal chelating agent. In addition, amphiphilic N,N’-disubstituted β-C-maltosylbarbiturates formed vesicle gels in pure water that were scarcely observed for glyco-hydrogelators. Finally, barbituric acid worked as a multitasking group allowing chemoselective ligation onto reducing-end carbohydrates, structural diversity, stimuli-sensitiveness, and supramolecular interactions by hydrogen bonding.

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