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3-(hexadecyloxy)propylamine is a chemical compound that possesses surfactant properties, allowing it to lower the surface tension between two liquids or a liquid and a solid. It is a member of the fatty amine ether family, with a structure that includes a long hydrocarbon chain for lipid solubility and an amine functional group for water solubility. 3-(hexadecyloxy)propylamine can be synthesized from hexadecanol and 3-bromopropylamine under specific conditions, and it requires careful handling due to safety concerns. While information on its toxicity, environmental impact, and specific uses or benefits may not be widely available or well-studied, its surfactant nature suggests potential applications in various industries.

4673-33-0

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4673-33-0 Usage

Uses

Used in Detergent Industry:
3-(hexadecyloxy)propylamine is used as a surfactant for its ability to reduce surface tension, which is essential in the formulation of detergents and soaps. This property helps in the dispersion of dirt and grease, making it easier to clean various surfaces.
Used in Soap Industry:
In the soap industry, 3-(hexadecyloxy)propylamine is used as a surfactant to facilitate the formation of lather and improve the cleaning efficiency of soap products. Its surfactant properties aid in the emulsification of oils and dirt, enhancing the soap's ability to clean.
Used in Cosmetics Industry:
3-(hexadecyloxy)propylamine is used as an ingredient in cosmetic products for its surfactant properties, which can help in the formulation of creams, lotions, and other skincare products. Its ability to reduce surface tension can improve the spreadability and absorption of these products on the skin.
Used in Industrial Cleaning:
3-(hexadecyloxy)propylamine is used as a surfactant in industrial cleaning applications, where its ability to lower surface tension can enhance the effectiveness of cleaning agents in removing dirt, grease, and other contaminants from various surfaces.
Used in Textile Industry:
In the textile industry, 3-(hexadecyloxy)propylamine is used as a surfactant to improve the wetting and cleaning properties of dye baths and other processing solutions. This can lead to more even dyeing and better overall fabric quality.

Check Digit Verification of cas no

The CAS Registry Mumber 4673-33-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,7 and 3 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4673-33:
(6*4)+(5*6)+(4*7)+(3*3)+(2*3)+(1*3)=100
100 % 10 = 0
So 4673-33-0 is a valid CAS Registry Number.
InChI:InChI=1/C19H41NO/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-18-21-19-16-17-20/h2-20H2,1H3

4673-33-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-hexadecoxypropan-1-amine

1.2 Other means of identification

Product number -
Other names EINECS 225-123-9

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:4673-33-0 SDS

4673-33-0Downstream Products

4673-33-0Relevant academic research and scientific papers

Lipophilic amines as potent inhibitors of N-acylethanolamine-hydrolyzing acid amidase

Yamano, Yumiko,Tsuboi, Kazuhito,Hozaki, Yuki,Takahashi, Kiyohiro,Jin, Xing-Hua,Ueda, Natsuo,Wada, Akimori

, p. 3658 - 3665 (2012/07/28)

N-Acylethanolamines (NAEs) including N-arachidonoylethanolamine (anandamide) and N-palmitoylethanolamine are endogenous lipid mediators. These molecules are degraded to the corresponding fatty acids and ethanolamine by fatty acid amide hydrolase (FAAH) or NAE-hydrolyzing acid amidase (NAAA). Lipophilic amines, especially pentadecylamine (2c) and tridecyl 2-aminoacetate (11b), were found to exhibit potent NAAA inhibitory activities (IC50 = 5.7 and 11.8 μM), with much weaker effects on FAAH. These simple structures would provide a scaffold for further improvement in NAAA inhibitory activity.

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