Formulation and evalution of herbal vanishing cream was written by Krishnan, Nived;Afsal, V. T. Ibrahim;Jamal, Farisha;Rasheed, Rinsha;Shahana, Sherin P. P.. And the article was included in World Journal of Pharmaceutical Research in 2022.Application In Synthesis of Glyceryl monostearate The following contents are mentioned in the article:
The skin is the largest organ of the body. There are three structural layers for skin-epidermis, dermis, and subcutis. Hair, nails, sebaceous gland, sweat gland and apocrine glands are regarded as derivatives of skin. There are different types of skin problems and the surge for discovering natural products. skin problem is one of the major problems in both mens and women. It may be due to certain hereditary factors, stress, alc. consumption, environmental factors etc This study aims to determine the potent skin care activity of herbal plant material, their extraction and to select the safest and effective formulation for their related problem. Crude drugs were obtained from local vendors. plant Curcuma longa (turmeric), Azadirachta indica (Neem) was collected and were carried out and formulated. The present work aimed to formulate herbal vanishing cream having antibacterial properties. Herbal vanishing cream is an o/w type emulsion formulated by using neem and turmeric. Then it is evaluated by using various parameters like appearance, pH, irritancy, smear test, spreadability etc. Antibacterial property of herbal vanishing cream was proved by using microbial assay. Hence it is confirmed that the formulated herbal vanishing cream shows better antibacterial properties, skin moisturizer, sheen effect, daily day creams, moisture locking power etc. This study involved multiple reactions and reactants, such as Glyceryl monostearate (cas: 31566-31-1Application In Synthesis of Glyceryl monostearate).
Glyceryl monostearate (cas: 31566-31-1) belongs to esters. Carboxylic acid esters of low molecular weight are colourless, volatile liquids with pleasant odours, slightly soluble in water. Many esters have the potential for conformational isomerism, but they tend to adopt an s-cis (or Z) conformation rather than the s-trans (or E) alternative, due to a combination of hyperconjugation and dipole minimization effects. The preference for the Z conformation is influenced by the nature of the substituents and solvent, if present. Lactones with small rings are restricted to the s-trans (i.e. E) conformation due to their cyclic structure.Application In Synthesis of Glyceryl monostearate
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics