Sodium (S)-2-tetradecanamidopropanoate

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Reagent Code: #236507
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CAS Number 67395-95-3

science Other reagents with same CAS 67395-95-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 321.43 g/mol
Formula C₁₇H₃₂NNaO₃
badge Registry Numbers
MDL Number MFCD09751069
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a chiral surfactant in pharmaceutical and cosmetic formulations, this compound enhances the solubility and stability of active ingredients while providing mild cleansing properties. Its enantiomerically pure structure supports improved biodegradability and skin compatibility, making it suitable for sensitive skincare products. It is also employed in chiral separation techniques and asymmetric synthesis due to its ability to form organized micellar structures that influence stereoselective reactions.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,590.00
inventory 250mg
10-20 days ฿3,200.00
inventory 1g
10-20 days ฿8,600.00
Sodium (S)-2-tetradecanamidopropanoate
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Used as a chiral surfactant in pharmaceutical and cosmetic formulations, this compound enhances the solubility and stability of active ingredients while providing mild cleansing properties. Its enantiomerically pure structure supports improved biodegradability and skin compatibility, making it suitable for sensitive skincare products. It is also employed in chiral separation techniques and asymmetric synthesis due to its ability to form organized micellar structures that influence stereoselective reactio

Used as a chiral surfactant in pharmaceutical and cosmetic formulations, this compound enhances the solubility and stability of active ingredients while providing mild cleansing properties. Its enantiomerically pure structure supports improved biodegradability and skin compatibility, making it suitable for sensitive skincare products. It is also employed in chiral separation techniques and asymmetric synthesis due to its ability to form organized micellar structures that influence stereoselective reactions.

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