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25054-76-6

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25054-76-6 Usage

General Description

"(Z)-(Carboxymethyl)dimethyl-3-[(1-oxo-9-octadecenyl)amino]propylammonium hydroxide" is a chemical compound known for its lengthy name and complex structure. It's a synthetic compound which doesn't naturally occur. It contains several different functional groups and a lengthy carbon chain. It comprises of a carboxymethyl group (a moiety derived from carboxylic acid), a dimethylammonium group, a propylammonium group, and an octadecenyl group joined together through a number of chemical bonds. (Z)-(carboxymethyl)dimethyl-3-[(1-oxo-9-octadecenyl)amino]propylammonium hydroxide follows the stereochemistry where the two principal groups have the Z configuration, meaning they are on the same side of the molecule. It is an acidic compound due to the presence of a hydroxide (OH-) ion. Details about its uses and properties might not be widely available, as such complex compounds are often the focus of research studies for potential applications in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 25054-76-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,0,5 and 4 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 25054-76:
(7*2)+(6*5)+(5*0)+(4*5)+(3*4)+(2*7)+(1*6)=96
96 % 10 = 6
So 25054-76-6 is a valid CAS Registry Number.
InChI:InChI=1/C25H48N2O3/c1-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-20-24(28)26-21-19-22-27(2,3)23-25(29)30/h11-12H,4-10,13-23H2,1-3H3,(H-,26,28,29,30)/b12-11-

25054-76-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[dimethyl-[3-[[(Z)-octadec-9-enoyl]amino]propyl]azaniumyl]acetate

1.2 Other means of identification

Product number -
Other names Oleamidopropyl betaine

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:25054-76-6 SDS

25054-76-6Synthetic route

(9Z)-N-[3-(dimethylamino)propyl]octadec-9-enamide
109-28-4

(9Z)-N-[3-(dimethylamino)propyl]octadec-9-enamide

sodium monochloroacetic acid
3926-62-3

sodium monochloroacetic acid

oleamidopropyl betaine
25054-76-6

oleamidopropyl betaine

Conditions
ConditionsYield
In ethanol; water at 79℃; for 12h;
cis-Octadecenoic acid
112-80-1

cis-Octadecenoic acid

1-amino-3-(dimethylamino)propane
109-55-7

1-amino-3-(dimethylamino)propane

oleamidopropyl betaine
25054-76-6

oleamidopropyl betaine

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: sodium fluoride; aluminum oxide / neat (no solvent) / 10 h / 155 - 160 °C / Inert atmosphere
2: water; ethanol / 12 h / 79 °C
View Scheme

25054-76-6Downstream Products

25054-76-6Relevant articles and documents

Synthesis and surface activities of amidobetaine surfactants with ultra-long unsaturated hydrophobic chains

Feng, Dan,Zhang, Yongmin,Chen, Quansheng,Wang, Jiyu,Li, Bin,Feng, Yujun

, p. 657 - 661 (2012/11/07)

Recent studies have shown that the surfactants bearing an ultra-long hydrophobic chain (>C18) exhibit unique self-assembly properties. However, their synthesis and surface activities have been less documented. In this work, monounsaturated alkyl dimethyl amidopropyl betaines, UCnDAB (n = 18, 22, and 24), were prepared by the reaction of the corresponding fatty acids with N,N-dimethyl-1,3-propanediamine, followed by quaternization with sodium choloroacetate of the obtained intermediates. The intermediates and final surfactants were characterized by 1H NMR and ESI-HRMS, respectively. Krafft temperature (TK) and surface activities of the surfactants were also examined. It was found that TK of all these surfactants is lower than 0°C, and their critical micellar concentration (CMC) is within the range of 10-3 mmol/L. In addition, the linear relationship between lg CMC and n is still in evidence.

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