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18375-63-8

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18375-63-8 Usage

General Description

N-dodecyl-D-gluconamide is a chemical compound derived from glucose and dodecanol. It is a non-ionic surfactant and is commonly used as an ingredient in cleaning, personal care, and cosmetic products. Due to its surfactant properties, it helps to lower the surface tension of water, allowing it to spread more easily and penetrate surfaces to remove dirt and oil. It is also known for its mildness on the skin, making it suitable for use in products such as shampoos, hand soaps, and body washes. Additionally, N-dodecyl-D-gluconamide is considered biodegradable and environmentally friendly, making it an attractive ingredient for use in various consumer products.

Check Digit Verification of cas no

The CAS Registry Mumber 18375-63-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,3,7 and 5 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 18375-63:
(7*1)+(6*8)+(5*3)+(4*7)+(3*5)+(2*6)+(1*3)=128
128 % 10 = 8
So 18375-63-8 is a valid CAS Registry Number.
InChI:InChI=1/C18H37NO6/c1-2-3-4-5-6-7-8-9-10-11-12-19-18(25)17(24)16(23)15(22)14(21)13-20/h14-17,20-24H,2-13H2,1H3,(H,19,25)/t14-,15-,16+,17-/m1/s1

18375-63-8SDS

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-dodecyl-D-gluconamide

1.2 Other means of identification

Product number -
Other names D-Gluconsaeure-dodecylamid

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:18375-63-8 SDS

18375-63-8Downstream Products

18375-63-8Related news

Research paperEnhancing water solubility of N-dodecyl-D-gluconamide (cas 18375-63-8) surfactant using borax08/27/2019

The N-dodecyl gluconamide surfactant (C12GA) was synthesized and characterized by infrared and 1H NMR spectroscopy. The solubility, surface activity and rheology in aqueous solution of mixed C12GA and borax were investigated by surface tension measurements, transmission electron microscopy and r...detailed

18375-63-8Relevant articles and documents

Synthesis and interfacial properties of new 6-sulfate sugar-based anionic surfactants

Abdellahi, Bemba,Bois, Rémy,Chagnault, Vincent,Drelich, Audrey,Golonu, Sema,Lesur, David,Nesterenko, Alla,Pezron, Isabelle,Pourceau, Gwladys,Wadouachi, Anne

supporting information, (2021/05/31)

Three families of anionic sugar-based surfactants bearing a sulfate functional group on the primary position of a monosaccharide were synthesized and their physicochemical properties were compared. The first family corresponds to 6-sulfate derivatives of commercially available octa- and dodecyl β-D-gluco- and galactopyranosides. The second and the third families contain an amide linker between the sulfated monosaccharide (galactose, glucose or xylose) and the hydrophobic alkyl chain. Twelve of the as-synthesized anionic glycolipids, including nine novel sulfated compounds, were investigated for their surface activity at the air/liquid interface and for their self-assembling properties. These sugar-based surfactants show surface properties similar to those of commercial anionic surfactants (SDS and SLES) with good ability to reduce surface tension. The obtained results confirm the interest in these new bio-based molecules for potential substitution of anionic surfactants in various formulations.

A New Family of Liquid Crystals: N-Substituted Aldonamides II: Relationship Between Chemical Structure and the Formation of Mesophases

Baeyens-Volant, D.,Fornasier, R.,Szalai, E.,David, C.

, p. 93 - 110 (2007/10/02)

A series of N-substituted aldonamodes has been synthesized.Some of these compounds form a thermotropic lamellar mesophase in which molecules in the trans-configuration are arranged in monolayers stabilized by hydrogen bonding and hydrophobic interactions.X-ray diffraction studies have shown that a molecular arrangement of this type exists in the crystalline solid of N-decylribonamide.The relationship between the mesogenic properties and the molecular structures of these compounds is discussed (with reference to the length, branching and cyclisation of the aldonic residue and of the hydrocarbon chain). Keywords: N-aldonamides, lamellar thermotropic phase, crystal structure determination

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