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Tetradecyl 2-hydroxypropanoate
"Descrizione"
by Whiz35 (11828 pt)
2023-Jul-27 12:42

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Tetradecyl 2-hydroxypropanoate (Myristyl lactate) is the ester produced by a catalyzed reaction of either natural or synthetic myristyl alcohol and lactic acid. The ester produced by the reaction is washed to remove any catalyst and unreacted lactic acid. The final product is further washed with alkali and neutralized.

The name describes the structure of the molecule

  • Tetradecyl - Refers to tetradecyl alcohol, a long-chain fatty alcohol.
  • 2-Hydroxypropanoate - Another name for lactic acid.

Description of raw materials used in production

  • Tetradecyl alcohol - A long-chain fatty alcohol that can be obtained from plant or animal sources.
  • Lactic acid (2-hydroxypropanoic acid) - Can be produced synthetically or derived from bacterial fermentation of carbohydrates.

Synthesis process

  • Esterification reaction - Tetradecyl alcohol reacts with lactic acid in the presence of an acid catalyst to form Tetradecyl 2-Hydroxypropanoate.

It appears as a clear to yellowish liquid or in solid form as a white powder. In liquid form at room temperature and in solid form below room temperature.

What it is used for and where

Cosmetics

It acts as an emollient, lubricating, texturising agent with properties of imparting shine and silkiness to hair and skin. Has a degree of water repellency.

Skin conditioning agent - Emollient. Emollients have the characteristic of enhancing the skin barrier through a source of exogenous lipids that adhere to the skin, improving barrier properties by filling gaps in intercorneocyte clusters to improve hydration while protecting against inflammation. In practice, they have the ability to create a barrier that prevents transepidermal water loss.  Emollients are described as degreasing or refreshing additives that improve the lipid content of the upper layers of the skin by preventing degreasing and drying of the skin. The problem with emollients is that many have a strong lipophilic character and are identified as occlusive ingredients; they are oily and fatty materials that remain on the skin surface and reduce transepidermal water loss. In cosmetics, emollients and moisturisers are often considered synonymous with humectants and occlusives.

Skin conditioning agent. It is the mainstay of topical skin treatment as it has the function of restoring, increasing or improving skin tolerance to external factors, including melanocyte tolerance. The most important function of the conditioning agent is to prevent skin dehydration, but the subject is rather complex and involves emollients and humectants that can be added in the formulation.

Dosage: at 0.5-2% levels and maximum concentration 25%.

Applications

  • Emollient - Tetradecyl 2-hydroxypropanoate acts as an emollient, helping to keep the skin soft and smooth.
  • Skin Conditioning - Can enhance the appearance and feel of the skin, making it look more moisturized and supple.
  • Solvent - It can act as a solvent in some cosmetic products, helping to solubilize other ingredients.
  • Texture Enhancers - Can be used to adjust the texture and viscosity of creams, lotions, and other skincare products.
  • Partially Natural Origin - Since it's derived from tetradecyl alcohol and lactic acid, it can be considered of partially natural origin.

Safety

It has not demonstrated toxicity, irritation or sensitisation at doses formulated as safe in cosmetic products.

Myristyl lactate studies

Typical commercial product characteristics Myristyl lactate

AppearanceWhite powder
Boiling Point    330ºC at 760 mmHg
Flash Point    147.1ºC
Density0.922 g/cm3
Vapor Pressure1.26E-05mmHg at 25°C
Refraction Index1.453
PSA46.53000
LogP4.61150
Purity99.8%
Assay99.8%
Dryness0.19%
Heavy Metal
<10ppm
Sulfated Ash
0.009%
Residue On Ignition
0.03%
Specific Gravity0.892-0.904
Titer11°C-14°C
Acid value3 max
Ester value166-185
Saponification value166-185
Iodine value1.0 max




  • Molecular Formula     C17H34O3
  • Molecular Weight      286.4
  • Exact Mass   286.25100
  • CAS  1323-03-1
  • UNII    1D822OC34X
  • EC Number   215-350-1
  • DSSTox Substance ID  DTXSID50862630
  • IUPAC  tetradecyl 2-hydroxypropanoate
  • InChl=1S/C17H34O3/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-20-17(19)16(2)18/h16,18H,3-15H2,1-2H3
  • InChl Key      BORJONZPSTVSFP-UHFFFAOYSA-N
  • SMILES  CCCCCCCCCCCCCCOC(=O)C(C)O
  • MDL number  
  • PubChem Substance ID    
  • RXCUI      1363720
  • HS Code     2918110000

Synonyms:

  • Tetradecyl lactate
  • Myristyl lactate




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