Stearyl heptanoate

Last updated
Stearyl heptanoate
Stearyl heptanoate.png
Names
Preferred IUPAC name
Octadecyl heptanoate
Other names
Tegosoft SH
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.060.041 OOjs UI icon edit-ltr-progressive.svg
EC Number
  • 266-065-4
PubChem CID
UNII
  • InChI=1S/C25H50O2/c1-3-5-7-9-10-11-12-13-14-15-16-17-18-19-20-22-24-27-25(26)23-21-8-6-4-2/h3-24H2,1-2H3 X mark.svgN
    Key: ABTZKZVAJTXGNN-UHFFFAOYSA-N X mark.svgN
  • CCCCCCCCCCCCCCCCCCOC(=O)CCCCCC
Properties
C25H50O2
Molar mass 382.673 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Stearyl heptanoate is the ester of stearyl alcohol and heptanoic acid (enanthic acid). It is used in cosmetics, [1] including eyeliner. It is prepared from stearyl alcohol, which may be derived from animal or vegetable sources.

Stearyl heptanoate is added to cosmetics to act as an emollient.

Related Research Articles

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<span class="mw-page-title-main">Oleyl alcohol</span> Chemical compound

Oleyl alcohol, or cis-9-octadecen-1-ol, is an unsaturated fatty alcohol with the molecular formula C18H36O or the condensed structural formula CH3(CH2)7−CH=CH−(CH2)8OH. It is a colorless oil, mainly used in cosmetics.

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Stearyl alcohol, or 1-octadecanol, is an organic compound classified as a saturated fatty alcohol with the formula CH3(CH2)16CH2OH. It takes the form of white granules or flakes, which are insoluble in water. It has a wide range of uses as an ingredient in lubricants, resins, perfumes, and cosmetics. It is used as an emollient, emulsifier, and thickener in ointments, and is widely used as a hair coating in shampoos and hair conditioners. Stearyl heptanoate, the ester of stearyl alcohol and heptanoic acid (enanthic acid), is found in most cosmetic eyeliners. Stearyl alcohol has also found application as an evaporation suppressing monolayer when applied to the surface of water.

Cetyl alcohol, also known as hexadecan-1-ol and palmityl alcohol, is a C-16 fatty alcohol with the formula CH3(CH2)15OH. At room temperature, cetyl alcohol takes the form of a waxy white solid or flakes. The name cetyl derives from the whale oil (cetacea oil, from Latin: cetus, lit. 'whale', from Ancient Greek: κῆτος, romanized: kētos, lit. 'huge fish') from which it was first isolated.

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Rice bran wax is the vegetable wax extracted from the bran oil of rice.

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Panthenol (also called pantothenol) is the alcohol analog of pantothenic acid (vitamin B5), and is thus a provitamin of B5. In organisms, it is quickly oxidized to pantothenic acid. It is a viscous transparent liquid at room temperature. Panthenol is used in pharmaceutical and cosmetic products as a moisturizer and to improve wound healing.

<span class="mw-page-title-main">Toner (skin care)</span> Type of cosmetics

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Ethyl heptanoate is the ester resulting from the condensation of heptanoic acid and ethanol. It is used in the flavor industry because of its odor that is similar to grape.

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Cetostearyl alcohol, cetearyl alcohol or cetylstearyl alcohol is a mixture of fatty alcohols, consisting predominantly of cetyl and stearyl alcohols and is classified as a fatty alcohol. It is used as an emulsion stabilizer, opacifying agent, and foam boosting surfactant, as well as an aqueous and nonaqueous viscosity-increasing agent. It imparts an emollient feel to the skin and can be used in water-in-oil emulsions, oil-in-water emulsions, and anhydrous formulations. It is commonly used in hair conditioners and other hair products.

The INCI names ceteareth-n (where n is a number) refer to polyoxyethylene ethers of a mixture of high molecular mass saturated fatty alcohols, mainly cetyl alcohol (m = 15) and stearyl alcohol (m = 17). The number n indicates the average number of ethylene oxide residues in the polyoxyethylene chain.

<span class="mw-page-title-main">Eye liner</span> Cosmetic applied around the eyes

Eye liner or eyeliner is a cosmetic used to define the eyes. It is applied around the contours of the eye(s). It is often used to create various aesthetic effects.

<span class="mw-page-title-main">Stearyl palmityl tartrate</span> Chemical compound

Stearyl palmityl tartrate is a derivative of tartaric acid used as an emulsifier. It is produced by esterification of tartaric acid with commercial grade stearyl alcohol, which generally consists of a mixture of the fatty alcohols stearyl and palmityl alcohol. Stearyl palmityl tartrate consists mainly of diesters, with minor amounts of monoester and of unchanged starting materials.

Stearalkonium chloride is a type of benzalkonium chloride which is used as an anti-static agent, a surfactant and an antimicrobial. It is an ingredient in some cosmetics and hair care products, particularly conditioners. It was originally designed by the fabric industry for use as a fabric softener.

<span class="mw-page-title-main">Hydroxyprogesterone heptanoate</span> Chemical compound

Hydroxyprogesterone heptanoate (OHPH), also known as hydroxyprogesterone enanthate (OHPE) and sold under the brand names H.O.P., Lutogil A.P., and Lutogyl A.P. among others, is a progestin medication used for progestogenic indications. It has been formulated both alone and in together with estrogens, androgens/anabolic steroids, and other progestogens in several combination preparations. OHPH is given by injection into muscle at regular intervals.

<span class="mw-page-title-main">Hydroxyprogesterone heptanoate benzilic acid hydrazone</span> Chemical compound

Hydroxyprogesterone heptanoate benzilic acid hydrazone (OHPHBH), also known as 17α-hydroxyprogesterone 17α-heptanoate 3-benzilic acid hydrazone, is a progestin medication which was never marketed. It is the C3 benzilic acid hydrazone of hydroxyprogesterone heptanoate (OHPH). The medication has a longer duration of action than OHPH when administered by subcutaneous injection in animals.

The molecular formula C25H50O2 (molar mass: 382.663 g/mol, exact mass: 382.3811 u) may refer to:

References

  1. Fiume, Monice M.; Bergfeld, Wilma F.; Belsito, Donald V.; Hill, Ronald A.; Klaassen, Curtis D.; Liebler, Daniel; Marks, James G.; Shank, Ronald C.; Slaga, Thomas J.; Snyder, Paul W.; Andersen, F. Alan (2012). "Safety Assessment of Stearyl Heptanoate and Related Stearyl Alkanoates as Used in Cosmetics". International Journal of Toxicology. 31 (5_suppl): 141S–146S. doi:10.1177/1091581812460408. PMID   23064772.