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4-(Phenylthio)benzyl alcohol is a versatile building block used in the synthesis of complex compounds. It has been shown to be an effective reagent for the synthesis of polymers and other organic molecules. 4-(Phenylthio)benzyl alcohol is also a useful intermediate for the preparation of chemical compounds with high quality, such as fine chemicals, speciality chemicals, and research chemicals. This compound can be used as a reaction component in the synthesis of valuable scaffolds.

AMPD, also known as 2-Amino-2-methyl-1,3-propanediol, is a buffer solution with a pH range of 7.8-9.7 and a pKa of 8.8. This chemical buffer is used in molecular biology, protein studies, enzyme assays, and separation techniques such as isatachophoresis (ITP) and SDS-gradient gel electrophoresis.

3β,22E)-29-Fluorostigmasta-5,22-dien-3-ol is a plant growth regulator that belongs to the group of fatty alcohols. It is found in the horticultural and tissue culture industries and is used as an additive in bioassays. 3β,22E)-29-Fluorostigmasta-5,22-dien-3-ol enhances the growth rate of nematodes and has been shown to be a potent inhibitor of benzoate degradation. This compound also has hormone effects that are similar to those of furostanols or steroids.

3-Chloro-4-methylbenzyl alcohol is a building block chemical that is used in the synthesis of a variety of organic compounds. It is a versatile chemical that can be used as a reagent, reaction component, and intermediate. 3-Chloro-4-methylbenzyl alcohol has been found to be useful in the synthesis of complex compounds, such as 4-chloromethoxybenzoic acid and 3-(3,5-dimethoxyphenyl)acetic acid. This chemical can also be used to produce speciality chemicals, such as 3-(2-(2,4-dichlorophenoxy)ethyl)benzonitrile.

Senkyunolide A is a bioactive compound, which is a type of phthalide derived from the roots of Ligusticum chuanxiong, a plant commonly used in traditional Chinese medicine. This compound is notable for its antioxidant and anti-inflammatory properties, which are believed to arise from its ability to scavenge free radicals and modulate inflammatory pathways.

3-Phenethylphenol is a hydrophobic, sterically-interacting compound that binds to molybdenum. It has been shown to inhibit the growth of fungi such as Poria and Coriolus. 3-Phenethylphenol also has functionalities such as peroxide, acetonitrile, and nature. This compound is not soluble in water and must be dissolved in solvents such as acetonitrile or polyvinyl acetate before use. 3-Phenethylphenol has been shown to have chromatographic properties, allowing it to be used as an adsorbent for the separation of organic compounds.

Xylene cyanol is a chemical compound that belongs to the group of phenols. It has been shown to be active in vitro against human skin cancer cells, and induces cell lysis. Xylene cyanol has also been found to bind to the BCR-ABL kinase domain, which is an enzyme that plays a crucial role in the development of leukemia and other autoimmune diseases. Xylene cyanol binds to dna binding domains on the protein surface and forms an adduct with bcr-abl kinase, which inhibits its activity. This inhibition prevents activation of this enzyme and leads to cell death by preventing DNA synthesis.

5-Methyl-2-nitrophenol is a phytotoxic chemical that is used as a synthetic intermediate in organic chemistry. It has been shown to have a high bioconcentration factor and can be found in wastewater. The major use of 5-methyl-2-nitrophenol is the synthesis of 2,4,6-trinitrophenylhydrazine (TNP) which is used as an analytical reagent for the determination of nitrates. The reaction mechanism of 5-methyl-2-nitrophenol involves intramolecular hydrogen transfer from the methylene group to the nitro group and subsequent elimination of HCl. This reaction product can be found by using analytical methods such as gas chromatography, mass spectrometry, or nuclear magnetic resonance spectroscopy. Functional groups on the reactant include phenols and nitro groups with the following endpoints: hydrochloric acid (HCl), kinetic method, and vapor pressure

7-Chloro-4-hydroxyquinoline-3-carboxylic acid is a chemical compound that has antioxidative activity and is used in the production of various organic substances. It is synthesized by reacting ammonium nitrate with a hydroxy group, an organic solvent, and phenoxy. The resulting product can be heated to form 7-chloro-4-hydroxyquinoline, which undergoes a series of reactions to produce 7-chloro-4-(2,2,2,-trichloroethoxy)quinoline. This reaction system produces a quinoline derivative that has been shown to be expressed at high levels in phosphatidylcholine (PC) and alpha-tocopherol (a vitamin E derivative). The final product is then purified by triethyl orthoformate (TEO), which removes the sulfoxide group.

5-Aminoquinoline (5-AQ) is a chemical compound that was originally synthesized in the 1930s. 5-AQ is a trifluoroacetic acid derivative of quinoline, which has been used as a photographic developer and an agent for the removal of silver from photographic film. This molecule also has a fluorescence property, which can be seen when irradiated by light with a wavelength greater than 350 nm. A hydrogen bond exists between the hydroxyl group and the nitrogen atom of the amine group in 5-AQ. The reaction mechanism for 5-AQ is believed to involve the diazonium salt intermediate, which reacts with silver ions to form silver diazonide and free ammonia.
5-AQ is insoluble in water but soluble in organic solvents such as acetone or alcohol. It reacts with trifluoroacetic acid to form a precipitate, which may be removed by filt

2,6-Dichlorophenolindophenol is a redox indicator that can be used as an optical sensor for the measurement of hydrogen peroxide and other reactive oxygen species. It has been shown to inhibit caspase-independent cell death in carcinoma cells and is active against the opportunistic fungus Candida glabrata. The optimum concentration for this compound has been determined to be 1 mM.

2-(3-Methylphenyl)ethanol is a benzene derivative that has been shown to be toxic at high doses. It is used as a solvent in dermatology and as an intermediate in the production of other chemicals. 2-(3-Methylphenyl)ethanol has been shown to have dermatologic effects such as erythema, scaling, and dryness. This compound also has a low degree of acute toxicity from ingestion or inhalation and is safe for use. The chemical structure consists of a benzene ring with two methyl groups on it, making it a primary alcohol.
2-(3-Methylphenyl)ethanol belongs to the class of alcohols. Alcohols are organic compounds containing one hydroxyl group attached to an alkyl or substituted alkyl radical. Alcohols can be classified according to their structure into primary, secondary, and tertiary alcohols, depending on how many carbon atoms are attached to the hydroxyl group

Tretoquinol is a bronchodilator, which is synthesized from specific chemical reactions involving quinoline derivatives. It functions primarily as a beta-adrenergic agonist, stimulating beta-2 adrenergic receptors. This activation leads to the relaxation of bronchial smooth muscle, resulting in widened air passages and improved airflow. Tretoquinol's mechanism of action involves enhancing cyclic adenosine monophosphate (cAMP) levels, which then promotes the relaxation of the bronchial and vascular musculature.

1-Naphthyl ethanol is a chromatographic solvent that is used in the reaction rate of lipase. It consists of two hydroxyl groups, one on each naphthalene ring. The hydroxyl groups are separated by a carbonyl group and a sterically hindered boron nitride. This compound is synthesized using triflic acid in methanol and reacts with carbinols to form functional groups. 1-Naphthyl ethanol has been shown to have stereoselective reactions with alkenes and alkynes, which may be due to its ability to form hydrogen bonds.

1-Palmitoyl-rac-glycerol is a fatty acid that contains nitrogen atoms. It has hypoglycemic effects and is used to treat metabolic disorders. 1-Palmitoyl-rac-glycerol has been shown to have a protective effect on the liver by decreasing the levels of triglycerides in the blood and preventing lipid peroxidation. It also improves glucose metabolism and insulin sensitivity. 1-Palmitoyl-rac-glycerol is an important component of biological membranes, where it forms a hydrophobic region that helps maintain membrane structure. This compound also has hemolytic activity, which may be due to its ability to bind with phospholipids or cell membranes, leading to changes in their permeability or stability. The stability of 1-palmitoyl-rac glycerol can be tested by adding reagents such as sodium nitrite or potassium permanganate, which will cause a color change from yellow to brown if it reacts

3-Bromo-4-chlorophenol (3BCP) is a halogenated phenolic compound that is used as a preservative in the food industry. It is also used in the chemical and pharmaceutical industries for polymerization reactions and to produce other chemicals such as chlorinated hydrocarbons. 3BCP has been shown to inhibit the growth of organisms by binding to their receptors, which can be deformed and thus not function properly. The affinity of 3BCP for these receptors can be rationalized by its chemical nature, which includes chlorine atoms that are nucleophilic and can form hydrogen bonds with other molecules. 3BCP has two isomers: 3-bromo-4-chlorophenol and 4-bromo-3-chlorophenol, each with different effects on organisms.

4-Hydroxy-3-nitrophenylacetic acid (4ONPA) is an organic compound that is the product of the reaction between hydroxylamine and nitrobenzaldehyde. It has been shown to have cytotoxicity in breast cancer cells and has been used as a probe for optical imaging studies. 4ONPA has also been shown to be able to inhibit the activity of enzymes such as catalase, peroxidase, and lipoxygenase. The uptake of 4ONPA into cells is dependent on its concentration and the cell type. This drug can be useful for treating degenerative diseases because it inhibits microglia activation by blocking the enzyme phospholipase A2. Clinical trials are currently being conducted for 4ONPA’s potential use in treating herpes simplex virus infections and cancerous lesions associated with Alzheimer's disease.

Amodiaquine is a drug that belongs to the class of antimalarial agents. It is used for the treatment and prevention of malaria caused by erythrocytic forms of Plasmodium falciparum. Amodiaquine has shown synergistic effects with other drugs, such as sulfadoxine and pyrimethamine, for the treatment of malaria due to P. falciparum. The mechanism of action of amodiaquine is not well understood, but it may involve inhibition of the Toll-like receptor. Amodiaquine has been shown to inhibit polymerase chain reaction in a concentration-dependent manner and also inhibits polymorphonuclear leucocytes, which are important in innate immunity. In addition, amodiaquine is a hypoglycemic agent and can be used for the treatment of bowel disease.

3-Hydoxy-2-nitrobenzyl alcohol is a high quality reagent that can be used as a complex building block, useful scaffold, and versatile building block for the synthesis of speciality chemicals. It is also used as a reaction component in the preparation of 3-hydroxy-2-nitrobenzyl chloride, which is an intermediate for the production of various pharmaceuticals. This chemical has a CAS number of 34112-74-8 and is classified as a research chemical.

3,4-Dimethyl-1H-pyrazol-5-ol is a fine chemical that belongs to the category of research chemicals. It has many uses as a reagent and as a speciality chemical. 3,4-Dimethyl-1H-pyrazol-5-ol is also a versatile building block and can be used as an intermediate or scaffold in complex reactions. The CAS number for this compound is 4344-72-3.

Carboxyethylsilanetriol sodium salt - 25% in water is a reagent that is used to form complex compounds. It can be used as a reaction component or a building block to create more complex compounds, such as new medicines. Carboxyethylsilanetriol sodium salt - 25% in water has been shown to be an efficient and versatile scaffold for the production of fine chemicals and research chemicals. CAS No. 18191-40-7 is a speciality chemical that can react with other organic compounds to form new compounds for research purposes. Carboxyethylsilanetriol sodium salt - 25% in water is a useful intermediate and building block for various synthetic reactions because it can easily react with other organics to form new compounds which are useful in pharmaceuticals, agrochemicals, and other industries.

4-Amino isoquinoline is a synthetic chemical that has a pyridine ring and chlorine atom. It can be synthesized by reacting 2,4-dichlorobenzene with acetaldehyde and hydrochloric acid. 4-Amino isoquinoline binds to the receptor that it interacts with, such as the ligand, dimethyl acetylenedicarboxylate, or taraxasterol acetate. This binding process can be used for treatment purposes. The ligand is usually introduced into the body through injection or ingestion of a drug. The ligand can also be attached to an antibody in order to target specific cells. The ligand has shown efficacy in treating cancerous tumors and other diseases like Parkinson's disease and Alzheimer's disease.

1,7-Heptanediol is a fatty acid that is used as a solvent and coating agent. It has been shown to inhibit leukemia cells in vitro. 1,7-Heptanediol has been shown to bind to the dna binding domains of transcription factors in vitro and may act as an anticancer agent by inhibiting the synthesis of proteins involved in biochemical pathways. 1,7-Heptanediol also inhibits tumor xenografts in vivo and induces apoptosis through hydrogen bond formation with DNA. It has been demonstrated to have detergent properties and can be used for biochemical reactions, such as the synthesis of chemical substances.

a-[2-(Methylamino)ethyl]benzyl alcohol is a zwitterion that forms an imine when reacted with piperazine. It has been shown to have antibacterial activity in subcritical water extraction and HPLC analysis. This compound also has a profile of impurities, including β-unsaturated aldehydes and pseudoephedrine.

4-[2-(4-Aminophenyl)ethyl]phenol belongs to the class of organogelators. It is an organic compound that has been used in various studies on supramolecular chemistry and catalytic rate research. 4-[2-(4-Aminophenyl)ethyl]phenol has been shown to form gels with a variety of solvents, including water, ethanol, and acetone. The compounds have also been studied for their ability to act as heterogeneously catalysts in the synthesis of polymers. These compounds are polymorphs, meaning they can exist in different crystal structures. Structural studies have revealed that these polymorphs display different architectures and reactivities.

4-Bromo-2,6-difluorobenzyl alcohol (4BDFA) is a molecule that has been shown to be able to produce magnetic resonance images. It can be used in tumor diagnosis as well as in the imaging of tumors. 4BDFA is synthesized by coupling 2,6-difluoroaniline with bromoacetaldehyde diethyl acetal. The syntheses are carried out under phase transfer catalysis conditions and the reaction is monitored by thin layer chromatography.
The synthesis of 4BDFA starts with the preparation of 2,6-difluoroaniline via a Grignard reaction between aniline and magnesium metal. The Grignard reagent is then added to bromoacetaldehyde diethyl acetal in dichloromethane followed by addition of triethylamine dropwise to maintain pH neutrality. The product is then extracted from the organic solution using ethyl ether

2-Phenyl-4-quinolinecarboxylic acid is a nonsteroidal anti-inflammatory drug that is commonly used to treat bronchoconstrictor response and inflammatory bowel disease. It is also an antimicrobial agent, which can be used to treat infectious diseases. The compound was found to have structural similarity to other nonsteroidal anti-inflammatory drugs, such as ibuprofen and naproxen. 2-Phenyl-4-quinolinecarboxylic acid has shown the ability to inhibit leukemia inhibitory factor (LIF) production by lymphocytes, which may have a role in the development of leukemia. This drug also possesses antioxidative properties and has been shown to have high values in group P2 polymerase chain reactions.

Triglycerides are a type of lipid that is composed of glycerol and three fatty acids. They are the main component of animal fats, vegetable oils, and butter. Triglycerids can be made by the reaction of glycerol with three molecules of fatty acid in the presence or absence of a catalyst. Triglycerols are also found naturally in many foods such as milk, meat, and eggs. The toxicity studies on triglycerides have shown that they are not toxic when ingested orally or intravenously at doses up to 500 mg/kg body weight. The reaction mechanism for the production of monolaurate from triglycerides is not well understood but it may involve the addition of hydroxyl groups to the fatty acid chains. This reaction is catalyzed by enzymes such as lipase, esterase, and alcohol oxidase. Triglycerides serve as an important source of energy for humans because they contain more than twice as much energy per gram than carbohydrates or proteins

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1-(3-Methylphenyl)ethanol is an organic compound that has a hydroxyl group, homochiral carbonyl group, and aromatic hydrocarbon. It is a product of the catalysed reaction between a hydroxyl compound and an alkyne molecule. The reaction mechanism begins with the formation of an imine intermediate. This intermediate then undergoes a double displacement to form the desired product and regenerate the catalyst. 1-(3-Methylphenyl)ethanol can be used as a building block for other organic compounds, such as epoxides or esters.

2,6-Dimethoxybenzyl alcohol is a synthetic compound that is a peroxidase substrate. It is used as an alternative for papaverine in the synthesis of penicillin and cephalosporin antibiotics. 2,6-Dimethoxybenzyl alcohol reacts with Mn2+ ions to form hydronium and hydrogen peroxide. This reaction has been shown to be more efficient than the decomposition of hydrogen peroxide by catalases or superoxide dismutases. 2,6-Dimethoxybenzyl alcohol also forms a reactive congener with erythrocytes and plasma proteins that can cause vasoconstriction in the blood vessels. The dimethoxybenzyl group (DMB) is a monosubstituted phenol group that binds to the active site of enzymes such as cytochrome P450s and glutathione reductase.

1,4-Dibromo-2,3-butandiol is a halogenated butandiol.

Xylenol orange tetrasodium salt is a fluorescent dye that can be used to measure the degree of mineralization in animal tissue. The dye is composed of xylenol, which is a fatty acid, and sodium chloride. Xylenol orange tetrasodium salt is used for measuring the rate of enzyme reactions by incubating it with the enzyme and measuring the formation rate. It has been shown to have damaging effects on mitochondria and tissues when exposed to an acidic environment. Xylenol orange tetrasodium salt binds to the membrane potential of cells in order to measure reactive oxygen species (ROS) production. This dye can also be used as a marker for autofluorescence of mitochondria and lipase activity.

3-Buten-3-ethyl-1-ol is a versatile building block that can be used as a reagent for chemical synthesis. It is a complex compound that can be used as a reaction component or intermediate in organic synthesis. 3-Buten-3-ethyl-1-ol has been shown to have antiinflammatory properties, which may be due to the inhibition of prostaglandin synthesis.

4-Methoxy propranolol is an intermediate in the synthesis of propranolol, a beta blocker.

The asymmetric synthesis of 4-chlorodiphenylcarbinol is an efficient method that uses a simple, inexpensive, and environmentally friendly reagent. The reaction proceeds in the presence of hydrochloric acid and sodium hydroxide solution. The reaction mechanism is the same as for the preparation of other chiral alcohols. The stereoselective preparation method is based on the use of glycol esters or trifluoroacetic acid to produce enantiomerically pure 4-chlorodiphenylcarbinol, which can be used as a precursor for pharmaceuticals, pesticides, and dyes.

Phenol red is a pH indicator that finds broad applications from chemistry to microbiology. Colour varies from yellow at pH<6.8 (lmax 443nm) through to light red/pink at 6.8<pH<8.2 (lmax 570 nm) to vivid purple/red at pH>8.2. It is widely used in cell culture to monitor pH and for colorimetric titration. For example, phenol red can be used to quantify Br- content in sea or fresh water. It is added to VTM as pH indicator, at the concentration of 10mg/ml, maintaining a pink colour at neutral pH.

(1-Methylpiperidin-2-yl)methanol is a gaseous organic acid that belongs to the piperazine class of compounds. It is used as an intermediate in the synthesis of various pharmaceuticals, including antipsychotics and antidepressants. (1-Methylpiperidin-2-yl)methanol has been shown to be an agonist of ganglion cells and can be used for the treatment of glaucoma. This compound also has shown to have anti-inflammatory properties, which may be due to its ability to inhibit nitric oxide production. Furthermore, (1-methylpiperidin-2-yl)methanol has been shown to inhibit 13c nuclear magnetic resonance spectroscopy with epoxides and hydroxyl groups. The reaction product is a crystalline solid with a molecular formula of C6H14O3N2, which corresponds to the molecular formula of 2-(dimethylam

Biotinyl-6-aminoquinoline is a synthetic chemical that has been shown to inhibit the growth of cancer cells in laboratory mice. It was synthesized to be a substrate for the enzyme quinolinate synthase, which is involved in the synthesis of nicotinic acid. Biotinyl-6-aminoquinoline is an analytical method that has been used in urinary samples from patients with bladder cancer as well as healthy individuals. The sequences of each individual were determined and analyzed using an algorithm that performs logistic regression, which can predict whether or not the patient has bladder cancer.

2-(4-Nitrophenoxy)ethanol (NPEO) is a water soluble, synthetic compound that has been shown to have anti-tumor properties. NPEO was found to be toxic to tumor cells in vitro and inhibits the growth of tumor cells in vivo. NPEO also inhibits the synthesis of DNA and RNA, which are important for cell division. This inhibitory effect may lead to the death of cancer cells by interfering with their ability to grow and divide.

2,4,6-Tribromo-3-methoxyphenol is a high quality reagent that is used as an intermediate in the production of many fine chemicals. It is also a useful building block for the synthesis of speciality chemicals and research chemicals. This chemical can be used as a versatile building block for reactions with other compounds. 2,4,6-Tribromo-3-methoxyphenol has CAS number 24967-79-1 and can be found at Chemical & Laboratory Equipment.

2,5-Dimethylresorcinol is a natural organic compound that has been shown to have the ability to inhibit the formation of reactive oxygen species. It is used in wastewater treatment and as an antioxidant. 2,5-Dimethylresorcinol has been shown to exhibit an inhibitory effect on lipid hydroperoxides and hydroxyl group binding. This compound can also be used as a substrate or product in catalytic domains. 2,5-Dimethylresorcinol is found in the form of usnic acid and orsellinic acid. The use of this compound as a catalyst for oxidation reactions has been studied extensively. It has also been shown to be an effective inhibitor for catalytic domains with a range of different metal ions.

Allopurinol is a drug that is used in the treatment of gout and other disorders caused by excessive production of uric acid. It functions as an inhibitor of xanthine oxidase, which is the enzyme responsible for converting hypoxanthine to xanthine, and xanthine to uric acid. Allopurinol blocks the conversion of these compounds, thereby reducing the formation of uric acid. Allopurinol has been shown to be effective for treating inflammatory bowel disease such as ulcerative colitis and Crohn's disease. This drug also inhibits nuclear DNA synthesis, antioxidant vitamins (e.g., vitamin E), and brain functions. Allopurinol has been shown to be effective in protecting neurons against oxidative injury that may lead to neurodegenerative diseases such as Parkinson's disease.

5α-Pregnan-3β-ol-20-one 3β-acetate is a synthetic steroid that is used to treat various neurological disorders, including dystonias, depression, and dyskinesias. It is an agonist of the GABA receptor and has been shown to have antidepressant effects in hamsters. 5α-Pregnan-3β-ol-20-one 3β-acetate has also been shown to have antiaggressive effects in mice and to decrease hormone levels in animals. The drug has been found to be safe for use in humans and does not affect fertility. 5α-Pregnan-3β-ol-20-one 3βacetate has been shown to be effective only when administered at high doses, which may be due to its poor oral bioavailability.

PEP is a "high-energy phosphate" compound playing a vital role in enzymatic phosphate-transfer reactions involved in ATP synthesis. It is used in conjunction with pyruvate kinase as a phosphorylating agent for ATP generation. Substrate for phosphoenolpyruvate carboxylase. Reagent for determination of glycerol.

20S-Protopanaxatriol is a drug that has been shown to have anticancer effects in human HL60 cells. It inhibits the expression of cytokines and inflammatory mediators, such as tumor necrosis factor-α (TNF-α), interleukin-6 (IL-6), and IL-8. 20S-protopanaxatriol also has anti-inflammatory properties due to its ability to inhibit toll-like receptor 4 (TLR4) activity. The drug may also be used for the treatment of chronic inflammation, arthritis, and other diseases related to TLR4 activation. This compound is an active ingredient found in ginseng and ginsenosides. These natural compounds are thought to work by binding to a response element on DNA and regulating the transcription of genes involved in immune responses or cell growth.

2-Aminophenol is a water soluble redox catalyst that is used in wastewater treatment. It has been shown to be a potent antimicrobial agent against bacteria, fungi, and viruses. 2-Aminophenol is active against the Gram-positive bacteria Staphylococcus aureus and Enterococcus faecalis. The mechanism of the reaction of 2-aminophenol with picolinic acid is believed to be due to intramolecular hydrogen bonding between nitrogen atoms (N) and amines (NH). The binding site for this reaction is not well understood, but it may involve an electrochemical mechanism such as constant pressure or electrochemical impedance spectroscopy. 2-Aminophenol also participates in electron transfer reactions involving NAD+/NADH or cytochrome c/cytochrome c oxidase.

4-Benzyl-5-(2-thienyl)-1,2,4-triazole-3-thiol (BTT) is a molecule that belongs to the class of thiourea derivatives. It has been used as an anti-inflammatory agent in animal models and has shown promising results for the treatment of human inflammatory diseases. BTT is a thiol which can reversibly bind to proteins by forming a covalent bond with the sulfur atom. This interaction inhibits the production of proinflammatory cytokines such as IL-6 and TNFα by inhibiting NFκB activation. The functional theory for BTT is based on its ability to prevent the formation of reactive oxygen species by inhibiting lipid peroxidation induced by ROS. In addition, BTT may suppress inflammation through inhibition of histamine release from mast cells.

Cetearyl alcohol is a type of fatty alcohol, which is derived from natural sources like coconut oil or palm kernel oil. It is a combination of cetyl and stearyl alcohols. This compound functions primarily through its emulsifying properties, allowing oil and water to mix effectively and form stable emulsions. It does this by reducing surface tension, thus facilitating the blending of disparate ingredients.