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Benzoic acid, 4-(hexadecyloxy)-3-methoxy-, also known as 3-methoxy-4-(hexadecyloxy)benzoic acid, is a chemical compound with the molecular formula C25H44O4. It is a derivative of benzoic acid, featuring a hexadecyloxy (C16H33O) group at the 4-position and a methoxy (CH3O) group at the 3-position. Benzoic acid, 4-(hexadecyloxy)-3-methoxy- is characterized by its long hydrocarbon chain, which contributes to its surfactant properties, making it useful in various applications such as emulsifiers, stabilizers, and foaming agents in the pharmaceutical, cosmetic, and industrial sectors. Its amphiphilic nature, with both hydrophilic (polar) and hydrophobic (non-polar) regions, allows it to interact with both water and oil, facilitating the formation of stable emulsions and dispersions.

5693-28-7

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5693-28-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5693-28-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,9 and 3 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5693-28:
(6*5)+(5*6)+(4*9)+(3*3)+(2*2)+(1*8)=117
117 % 10 = 7
So 5693-28-7 is a valid CAS Registry Number.

5693-28-7Downstream Products

5693-28-7Relevant academic research and scientific papers

Synthesis and thermal properties of cholesteryl 4-n-alkoxy-3-methoxybenzoates

Kasuga, Kazuyuki,Hatakeyama, Hyoe,Hatakeyama, Tatsuko

, p. 1 - 14 (2007/10/02)

A homologous series of new liquid crystalline compounds, cholesteryl 4-n-alkoxy-3-methoxybenzoate were synthesized from vanillin and their mesomorphic properties were studied by differential scanning calorimetry, polarizing microscopy and x-ray diffractometry.Each of the homologues from cholesteryl 3,4-dimethoxybenzoate (n=1) to cholesteryl 4-n-hexyloxy-3-methoxybenzoate (n=6) showed a cholesteric-nematic phase (NCh).The other higher homologues (from n=7 to n=18) indicated smectic A (SA) and NCh phases.The temperature region of smectic phases increased with the increase of the chain length of the n-alkoxy group.Transition temperatures in each of the homologues were lower than those in a corresponding non-3-methoxy substituted benzoate ester, due to the destabilizing effect of the lateral methoxy group.The effect was more significant on the homologues having a shorter n-alkoxy chain.It was also found that these esters formed a glassy state by quenching from mesophases and/or the isotropic liquid phase.The change of the glass transition temperature on each homologue (from n=1 to n=6) suggested the effect of the chain length of the n-alkoxyl group on the formation of the glassy state.Keywords: liquid crystals, thermal properties, differential scanning calorimetry, cholesteric phas, smectic A phase, glassy phase.

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