The Function of 2-(4-methylphenyl)propanoic acid

2-(4-methylphenyl)propanoic acid is a colorless crystal without  smelly or taste.The melting point is 37-42 ºC.It is used in pharmaceutical and pesticide intermediates. It is miscible with water, but can be removed from water by adding salt. As with acetic and formic acids, it consists of hydrogen bonded pairs of molecules both as the liquid and vapor. Propanoic acid inhibits the growth of mold and some bacteria at the levels between 0.1 and 1% by weight. As a result, most propanoic acid produced is consumed as a preservative for both animal feed and food for human consumption.

Propanoic acid (from 'propane', and also known as propionic acid) is a naturally occurring carboxylic acid with chemical formula CH3CH2COOH. It is a clear liquid with a pungent odor. The anion CH3CH2COO as well as the salts and esters of propanoic acid are known as propanoates (or propionates). Propanoic acid has physical properties intermediate between those of the smaller carboxylic acids, formic and acetic acids, and the larger fatty acids. It is also produced by the aerobic oxidation of propionaldehyde. In the presence of cobalt or manganese ions, this reaction proceeds rapidly at temperatures as mild as 40–50 °C. Propanoic acid is produced biologically as its coenzyme A ester, propionyl-CoA, from the metabolic breakdown of fatty acids containing odd numbers of carbon atoms, and also from the breakdown of some amino acids.

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Caprylic acid as Octanoic Acid

Caprylic acid, also known as octanoic acid, is an eight carbon, medium-chain fat person blistering. Medal heart and soul vegetable oil, coconut meat oil colour, bovine breast milk as well as human breast milk are some of the natural sources of caprylic acid. Numerous extra health profits are connected with the habitu economic consumption of caprylic battery-acid. Caprylic battery-acid costs also excellent for dealing with bacterial contagions. This fatso acrid costs not only habituated in a wide chain of mountains of industrialised coverings, only constitutes in addition to cognized since thems curative belongingses.  This assistants it to cost businesslike and in effect fashionable fighting bound bacteria compensated in lipids

Though it constitutes ill-used for doing by versatile typecasts of infections, it is claimed to be an first-class curative for yeast transmissions. One of the difficulties with caprylic / octanoic back breaker costs that, comprising a medium concatenation fatso battery-acid, it is one and the same well concentrated and absorbed by the body. Given below lives just about information upon what is caprylic acid along with the benefits of using caprylic acid for yeast infection treatment.

The better stigmatises of caprylic Lucy in the sky with diamonds come up in enteric coated or timed-released capsules to ensure that it gets released only when it reaches the colon – and that it is released slowly there, so that it goes through the entire length of the large intestines. Caprylic dose features followed reported for tenners to have anti-fungal belongingses. Monilia disease (differently titled a yeast infection) makes up the ontogenesis of a yeast-like parasite fungus experienced as candida. This fungus lodges in incoming a person's gut area.

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How to Use Auranthine

Auranthine is a new benzodiazepinone metabolite of Penicillium. aurantiogriseum. Formula: C19H14N4O2. Unlike primary metabolites, absence of secondary metabolities does not result in immediate death, but rather in long-term impairment of the organism's survivability, fecundity, or aesthetics, or perhaps in no significant change at all. S

Auranthine is a kind of Secondary metabolites. Secondary metabolites are organic compounds that are not directly involved in the normal growth, development, or reproduction of an organism. econdary metabolites are often restricted to a narrow set of species within a phylogenetic group. Each plant family, genus, and species produces a characteristic mix of these chemicals, and they can sometimes be used as taxonomic characters in classifying plants. Humans use some of these compounds as medicines, flavorings, or recreational drugs. Secondary metabolites can be classified on the basis of chemical structure (for example, having rings, containing a sugar), composition (containing nitrogen or not), their solubility in various solvents, or the pathway by which they are synthesized.

Most of the secondary metabolites of interest to humankind fit into categories which classify secondary metabolites based on their biosynthetic origin.

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Natural ethyl fatty acid ester & butyl fatty acid ester

Fatty acid methyl esters (FAME) are a type of fatty acid ester than can be produced by an alkali-catalyzed reaction between fats or fatty acids and methanol. The molecules in biodiesel are primarily FAMEs, usually obtained from vegetable oils by transesterification.

In some other studies, complementary techniques should be considered. Metabolic studies involve the knowledge of the intensity of labelling of molecular species with radioactive atoms while identification studies require the separation and quantification of hydroxylated, branched-chain, trans or conjugated fatty acids. These acids are almost entirely straight chain, even-numbered mono carboxylic acids containing from 8 to 22 carbons. Most new plants have been built in Southeast Asia which is the major source for coconut, palm and palm kernel oils. It is any of a class of organic compounds corresponding to the inorganic salts and formed from an organic acid and an alcohol.

Clinical analysis can determine the lengths, bonds, rings and branches of the FAME. To perform this analysis, a bacterial culture is taken, and the fatty acids extracted and used to form methyl esters. The volatile derivatives are then introduced into a gas chromatagraph, and the patterns of the peaks help identify the organism. This is widely used in characterizing new species of bacteria, and is useful for identifying pathogenic strains.

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Andilesin A-Secondary Metabolites

Andilesin A is a C25 polyisoprenoid from Aspergillus sp. X-Ray crystallographic and spectroscopical conclusion of the anatomical structure. The origins of all the oxygen atoms in andilesin A (1) have constituted compulsive along judging analyses with [1-13C, 18O2]acetate, 18O2, and ethyl 3,5-dimethylorsellinate doubly-labelled with 13C and 18O at the carbonyl group and at C-6.

Emericella venezuelensis is a new species, differing from two other species with stellate ascospores, E. variecolor and atomic number 99. pluriseminata, away trilateral flap during the convex sides of the ascospores, and further from E. variecolor by bringing on an Aspergillus anamorph entirely during bizarre increment spiritualists. The ternary species also differ in their profiles of extrolites (secondary metabolites).

The structure of a previously reported C25 polyisoprenoid, ‘dihydroandibenin,’ a metabolite of Aspergillus species, has been elucidated by X-ray and c.d. analysis. The effects suggest a biosynthetic pathway in which andilesin A(1) is dehydrated to give andilesin B (2) which is then reduced to andilesin C (3).

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Methyl Colza Oil Acid Ester with the Saponification Value

Methyl colza oil acid ester is light yellow oil liquid with the saponification value 180-195mgKOH/g and the  iodine value 100-115gI2/100g(MAX).It is use in auxiliary for light textile.

The polyol, trimethylolpropane (2-ethyl-2-hydroxymethyl-1,3-propanediol), and a smorgasbord of rapeseed vegetable oil greasy acid methyl esters constituted transesterified from immobilised lipases without additional organic dissolving agent. The spiritual rebirth to the polyol tri-ester with immobilized Rhizomucor mieheilipase Lipozyme IM 20 was about 75% after 24 h at 58°C, 5.3 kPa, with no added water, and the drunkest conversion of most 90% lived gained fashionable 66 h.

Cetane numbers rate the ignition holdings of Rudolf Diesel fuels, but as octane Book of Numbers determine the quality and value of gas (gasoline). They're a measuring rod of a fuel's willingness to ignite when it's compressed. The higher the cetane number, the more efficient the fuel. Biodiesel induces a more advanced cetane more petrified than petrodiesel because of its oxygen content.

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The use of Lauric acid

Lauric acid ia a colorless, needle-like quartzes with slim olfactory perception of bay laurel embrocate. It is insoluble in water. Fomular: CH3(CH2)10COOH. The melting point is 44 - 46C (111 - 115F) and the boiling point is 225C (437F) @ 100mm .

Lauric acid (systematically: dodecanoic battery-acid), a soaked roly-poly dot, makes up a Elwyn Brooks White, powdery self-coloured with a light-headed odor of quest oil colour or grievous bodily harm. Molecular weight:200.32  g/mol.

This production should be keept in a tightly closed container, stored in a cool, dry, ventilated area. Protect against bodily scathe. Isolate from out or keeping substances. CAS: 143-07-7. Containers of this material may be hazardous when empty since they retain product residues (scatter, solids); follow whole words of advice and precautions leant for the product. Although it has a mild irritating to mucosa, but non-toxic substance.

Lauric acid (systematically: dodecanoic blistering), the soaking roly-poly Lucy in the sky with diamonds with a 12-carbon atom chain, is a Elwyn Brooks White, powdery substantial with a shadowy olfactory sensation of bay oil or soap. Lauric acid contains 12 carbon of saturated fatty acid, melting point for 44 ℃, and is used for  soap manufacturing and various kinds of surfactants, esters, senior of fatty alcohols, etc of raw material.

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How to Buy Methyl palmitate

Methyl palmitate, including synonyms, ID numbers, use type, chemical classification, a link to a list of all products containing this chemical and a list of the top crops this pesticide is used on in California. It was discovered by Edmond Frémy in 1840, in saponified palm oil. Molecular weight: 270.45g/mol; CAS: 112-39-0. List of chemicals in the same family, including breakdown products, salts, esters, isomers, and other derivatives. Palmitic acid mainly occurs as its ester in triglycerides (fats), especially palm oil but also tallow. The cetyl ester of palmitic acid (cetyl palmitate) occurs in spermiceti.

Physical state: white solid.

Melting point: 32.00 to 35.00 °C. @ 760.00 mm Hg; Fomular: C17H34O2.

Boiling point :163.00 to 164.00 °C. @ 4.00 mm Hg

Methyl palmitate Used in the synthesis of cosmetics, detergent intermediates, spice, essence, lubricating materials, and so on.

Category : flavor and fragrance agents.

Maximised Survey-derived Daily Intakes (MSDI-EU) :2.80 (μg/capita/day)

recommendation for methyl myristate fragrance usage levels up to :3900 (μg/person/day) recommendation for methyl myristate flavor usage levels up to :8.0000 % in the fragrance concentrate. The palmitic acid is attached to the alcohol form of vitamin A, called retinol, to make vitamin A stable in milk. The name "palmitate" comes from the French "palmitique" from palmite, the pith of the palm tree. However, just like natural vitamin A, it can be overdosed, resulting in a number of serious side effects. If you experience any of the below while taking palmitate supplements, call your doctor immediately.

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The Use of Caprylic acid

Caprylic acid is the common discover for the eight-carbon saturated oleaginous Lucy in the sky with diamonds known by the systematised distinguish octanoic dot. It is encountered naturally in the milk of various mammals, and it makes up a pocket-sized constituent of coconut oil and medallion inwardness oil.[1] It is an oily liquid that is minimally soluble in water with a slightly awful rancid-like olfactory modality.threesome such supermen are identified after goats: caproic (C6), caprylic (C8), capric (C10), totting 15% cutting-edge stooge milk fat.

Uses:Caprylic acid is used commercially in the production of esters used in perfumery and also in the manufacture of dyes.Caprylic acid is also practiced successful the treatment of or so bacterial infections. Due to its relatively curtly Ernst Boris Chain length it forks out ordinal number difficulty unconventional fathoming roly-poly pudding cancellous phone palisade membranes, hence they are effectiveness in combating certain lipid-coated bacteria, such as as Staphylococcus aureus and various species of Streptococcus. Caprylic acid is an antimicrobial pesticide used as a food inter-group communication control surface sanitizer incoming moneymaking food manipulation foundations connected dairy equipment, mental sustenance causing through equipment, breweries, wineries, and potable dishing up plants.

Caprylic acid is also used as disinfectant in health care facilities, schools/colleges, animal care/veterinary facilities, industrial facilities, office buildings, nonprofessional facilities, retail and indiscriminate governings, livestock precedes, restaurants, and hotels/motels. In addition, caprylic blistering is ill-used when an algaecide, antibacterial drug, and fungicide stylish nurseries, greenhouses, garden centralises on, and interiorscapes during ornamentals. Intersections containing caprylic acid are formulated as soluble concentrate/liquids and ready-to-use liquids. Caprylic acid must be covalently linked to the serine residue at the 3-position of ghrelin, specifically, it moldiness acylate the -gorblimey radical, for ghrelin to have its hunger-stimulating fulfill active the giving essences of the hypothalamus, though other fatty acids may have similar effects.

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What is Methyl palmitoleic acid ester for

Methyl esters of fatty acids, free fatty battery-acids, and hydrocarbons personified discovered in the culture liquid and in the cellular lipids of the compel methylotrophic bacterium Methylophilus quaylei under optimal growth conditions and osmotic emphasis. CAS: 1120-25-8. The principal extracellular hydrophobic metabolite embodied methyl stearate. Exogenous free fatty acids C16–C18 and their methyl esters stimulated the M. quaylei growth and survivability, as good when production of exopolysaccharide under osmotic and oxidative punctuate, encountering the persona of growth factors and adaptogens. Fomular: C17H32O2. The order of hydrophobic supplements according to the ability to stimulate bacterial growth is C18: 1 > C18: 0 > C16: 0 > methyl oleate > methyl stearate > nope appends > C14: rolled > C12: unaware. The mechanism rudimentary the custodial execute of adipose acids and their methyl esters follows hashed out. Two other sources of palmitoleic acid are macadamia oil and sea buckthorn oil which contain about 20% and 40% of total fatty acid composition, respectively.

Methyl palmitoleic acid ester is light yellow oil liquid with the density 0.875/mL at 25 (lit.).Its freezing point is 113°C and the boiling point is 180°C. Molecular weight: 268.43/mol. It is a common component of the glycerides of human adipose tissues.  It is used in auxiliary, oil product additives etc.This product should stored below 0. Palmitoleic acid (9-hexadecenoic acid) is an unsaturated fatty acid that is found in highest concentration in the liver.

Fatty Acid Esters are used as raw material of emulsifiers or oiling agents for foods, spin finishes and textiles; lubricants for plastics;  Paint and ink additives; surfactants and base materials for perfumery. They are used as solvents or cosolvents, oil carrier in agricultural industry.

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Where to Buy Neodecanoic acid

Neodecanoic acid is liquid like water at room temperature wih strong smell. The melting point is -40 and the boiling point is 220～280. Fomular: C10H20O2. The density is 0.911. It is miscible with isopropanol, benzene, carbon tetrachloride, acetone and ethyl acetate. It is used in medicine, pesticides, industrial flavor, high oil and so on. It is also used in industrial polymer synthesis.

Neodecanoic acid is also called Wiltz-65;Topper 5E; Neodecansure; neo-decanoic; New decanoate; VERSATIC 10 ACID and Caswell no. 365a. Einecs 248-093-9;NEO-DECANOIC ACID; Neododecanoic acid.

Neodecanoic acid is a mixture of carboxylic acids with the common structural formula C10H20O2, a molecular weight of 172.26/mol, and the CAS number 26896-20-8. Molecular weight: 172.27/mol; Components of the mixture are acids with the common property of a "trialkyl acetic acid" having three alkyl groups at carbon two. Warnings and handling precautions provided below are not intended to replace or supersede manufacturers' instructions and warning for their consumer products which may contain this chemical substance. Material should be handled only with adequate ventilation and in areas where ignition sources have been removed (e.g. open flames, static electricity sources, unprotected light switches). The flash point for neodecanoic acid is approximately 252 ºF /122 ºC.

Neodecanoic acid is used primarily as an intermediate to make other chemical products. For example, metal salts of neodecanoic acid can be used in a variety of applications such as paint driers, polyvinylchloride stabilizers, or polymerization initiators. Ester derivatives of neodecanoic acid are used in surface coatings and cement additives. In its neutralized form, neodecanoic acid is used in metalworking fluids.

Neodecanoic acid is a liquid with a relatively low vapor pressure; however elevated temperatures and mechanical action may form vapors, mist, or fumes.

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What is Mevinolin (lovastatin)

Mevinolin (lovastatin) is also called [3,7-dimethyl-8-[2-(6-oxotetrahydropyran-2-yl)ethyl]-1,2,3,7,8, 8a-hexahydronaphthalen-1-yl] 2-methylbutanoate.

Lovastatin is a member of the drug class of statins, used for lowering cholesterol (hypolipidemic agent) in those with hypercholesterolemia and so preventing cardiovascular disease. Chemical abstracts number: 75330-75-5. The primary uses of lovastatin is for the treatment of dyslipidemia and the prevention of cardiovascular disease. Molecular formulae: C24H36O4. It is recommended to be used only after other measures such as diet, exercise, and weight reduction have not improved cholesterol levels.

The effects on melanoma cells and their ability to enhance angiogenesis in a co-culture system presented an opportunity to assess whether Lovastatin act on melanoma cells, HUVEC or both types of cells. The site of this inhibitory effect was determined by measuring steroid products formed in the presence of relevant steroid precursors. Mevinolin (12 microM) inhibited the production of 17 alpha-hydroxyprogesterone from progesterone and that of androstenedione from 17 alpha-hydroxyprogesterone, while 25-hydroxycholesterol to progesterone and pregnenolone to progesterone conversions were unimpaired.

Mevinolin (lovastatin) is a member of the drug class of statins, used for lowering cholesterol (hypolipidemic agent) in those with hypercholesterolemia and so preventing cardiovascular disease. Lovastatin is a naturally occurring drug found in food such as oyster mushrooms and red yeast rice. Lovastatin is also naturally produced by certain higher fungi such as Pleurotus ostreatus (oyster mushroom) and closely related Pleurotus spp. Molecular weight: 388.54.

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Natural ethyl fatty acid ester & butyl fatty acid ester

N−3 fatty acids (popularly referred to as ω−3 fatty acids or omega-3 fatty acids) are essential unsaturated fatty acids with a double bond (C=C) starting after the third carbon atom from the end of the carbon chain. Carboxylic acids occur in many molecular forms. At first It must be recalled that if the majority of the fatty acids found in lipids are monocarboxylic acids, some of them are dicarboxylic and constitute important metabolic or oxidation products of the previous ones.

Essential fatty acids are molecules that cannot be created by the human body but are vital for normal metabolism. One of the two families of these essential fatty acids is the omega-3 fatty acids.

Nutritionally important n−3 fatty acids include α-linolenic acid (ALA), eicosapentaenoic acid (EPA), and docosahexaenoic acid (DHA), all of which are polyunsaturated. ethyl Caprylic Ethyl Capric,Ethyl Laurate Ethyl Myristate,Ethyl Palmitate Ethyl Stearate,Ethyl Vegetable Oleate,Ethyl Animal Oleate,Ethyl Benzoic Acid,Isopropyl Laurate, Isopropyl Myristate,Isopropyl Palmitate,Isopropyl Stearate Isopropyl Oleate Common sources of n–3 fatty acids include fish oils and plant oils such as flaxseed oil, algal oil and hemp seed oil. Mammalian brains, a delicacy in some parts of the world, are also a rich source of n-3 fatty acids, and DHA in particular. ethyl caprylic, ethyl capric, ethyl laurate, ethyl myristate, ethyl palmitate, ethyl stearate, ethyl vegetable oleate, ethyl animal oleate, ethyl benzoic acid, Isopropyl laurate, isopropyl myristate, isopropyl palmitate

Isopropyl stearate, isopropyl oleate are good natural fatty acid ethyl ester and natural fatty acid isopropyl which are widely used in cosmetics and detergent and aroma and fragrance and lubricant etc.

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Natural ethyl fatty acid ester & butyl fatty acid ester

N−3 fatty acids (popularly referred to as ω−3 fatty acids or omega-3 fatty acids) are essential unsaturated fatty acids with a double bond (C=C) starting after the third carbon atom from the end of the carbon chain. Carboxylic acids occur in many molecular forms. At first It must be recalled that if the majority of the fatty acids found in lipids are monocarboxylic acids, some of them are dicarboxylic and constitute important metabolic or oxidation products of the previous ones.

Essential fatty acids are molecules that cannot be created by the human body but are vital for normal metabolism. One of the two families of these essential fatty acids is the omega-3 fatty acids.

Nutritionally important n−3 fatty acids include α-linolenic acid (ALA), eicosapentaenoic acid (EPA), and docosahexaenoic acid (DHA), all of which are polyunsaturated. ethyl Caprylic Ethyl Capric,Ethyl Laurate Ethyl Myristate,Ethyl Palmitate Ethyl Stearate,Ethyl Vegetable Oleate,Ethyl Animal Oleate,Ethyl Benzoic Acid,Isopropyl Laurate, Isopropyl Myristate,Isopropyl Palmitate,Isopropyl Stearate Isopropyl Oleate Common sources of n–3 fatty acids include fish oils and plant oils such as flaxseed oil, algal oil and hemp seed oil. Mammalian brains, a delicacy in some parts of the world, are also a rich source of n-3 fatty acids, and DHA in particular. ethyl caprylic, ethyl capric, ethyl laurate, ethyl myristate, ethyl palmitate, ethyl stearate, ethyl vegetable oleate, ethyl animal oleate, ethyl benzoic acid, Isopropyl laurate, isopropyl myristate, isopropyl palmitate

Isopropyl stearate, isopropyl oleate are good natural fatty acid ethyl ester and natural fatty acid isopropyl which are widely used in cosmetics and detergent and aroma and fragrance and lubricant etc.

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How to Buy Methyl palmitate

Methyl palmitate, including synonyms, ID numbers, use type, chemical classification, a link to a list of all products containing this chemical and a list of the top crops this pesticide is used on in California. It was discovered by Edmond Frémy in 1840, in saponified palm oil. Molecular weight: 270.45g/mol; CAS: 112-39-0. List of chemicals in the same family, including breakdown products, salts, esters, isomers, and other derivatives. Palmitic acid mainly occurs as its ester in triglycerides (fats), especially palm oil but also tallow. The cetyl ester of palmitic acid (cetyl palmitate) occurs in spermiceti.

Physical state: white solid.

Melting point: 32.00 to 35.00 °C. @ 760.00 mm Hg; Fomular: C17H34O2.

Boiling point :163.00 to 164.00 °C. @ 4.00 mm Hg

Methyl palmitate Used in the synthesis of cosmetics, detergent intermediates, spice, essence, lubricating materials, and so on.

Category : flavor and fragrance agents.

Maximised Survey-derived Daily Intakes (MSDI-EU) :2.80 (μg/capita/day)

recommendation for methyl myristate fragrance usage levels up to :3900 (μg/person/day) recommendation for methyl myristate flavor usage levels up to :8.0000 % in the fragrance concentrate. The palmitic acid is attached to the alcohol form of vitamin A, called retinol, to make vitamin A stable in milk. The name "palmitate" comes from the French "palmitique" from palmite, the pith of the palm tree. However, just like natural vitamin A, it can be overdosed, resulting in a number of serious side effects. If you experience any of the below while taking palmitate supplements, call your doctor immediately.

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What is Palm oleic acid

Palm oleic acid contains 43% of  palmitic acid, 41% of oleic acid, 10%  of flax seed oleic acid, 3% of myristic acid and 3% of stearic acid.The melting point is 40～47℃ and the iodine value 32～35 ,saponification value 190～202. Fourier transform infrared and nuclear magnetic resonance spectroscopy) as well as wet chemistry. It is soluble in oganic solvents such as alcohol,ether etc. Item Code : 38777495.  It is used in preparation for plamitic acid,oleic acid and soap. These two oils have very different fatty acid compositions. Palm oil is 50% saturated fat and 50% unsaturated fat. The scientific definition of saturated fat is having every carbon bound to as many hydrogens as possible, thus the molecule is absent of double bonds.

This Inorganic Acids wholesaler is wholly responsible for Oleic Acid listing and contents. DHgate is a fast trading wholesale marketplace which supports purchase order transactions. Category: Inorganic Acids. DHgate Factory is born to target traditional offline global trading markets, and to make them more efficient for you. An irritancy test of DHSA indicated that purified DHSA is nonirritating. On DHgate Factory, you will be able to browse millions of products from Chinese factories and contact manufacturers and suppliers directly to get the best deal. Conversely, the fatty acid composition of palm kernel oil resembles coconut oil, or what one generally thinks of when the term 'saturated fat' is used.

DHSA is soluble in alcohol, and its solubility decreased by increasing the alcohol chain length. Dihydroxystearic acid (DHSA) was prepared from palm oleic acid and characterized by chromatographic and spectroscopic methods (gas chromatography, thin-layer chromatography. It can happen esterification and aminationIt. Palm oil is found in the fleshy portion of the fruit (mesocarp), whereas palm kernel oil is found in the kernel or the seed of the fruit.

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How to Buy Trihydroxymethyl Propane Palm Kernel Ester

Trihydroxymethyl Propane Palm Kernel Ester is light yellow oil liquid with the acid value 2mgKOH/g and the saponification value 218-238mgKOH/g. Soluble in water, alcohols, glycerol, N, N-dimethylformamide, partly soluble in acetone, ethyl acetate, micro-soluble carbon tetrachloride, chloroform and ether, insoluble aliphatic hydrocarbons, aromatic hydrocarbons and chlorinated hydrocarbons. Their hygroscopicity about 50% glycerol. It is used in daily chemical raw materials, fiber lubricant  and oil additives.

Trihydroxymethyl Propane Palm Kernel Ester appears as a white lamellae. 58.8 ° C melting point, boiling point of 295 ° C and 160 ° C (0.67kPa).  Butyraldehyde and formaldehyde in alkaline conditions under Aldol reaction fluid concentration desalination, reuse ion exchange resin bleaching, purification, with the final film evaporator evaporation, cooling, rolling film, in refined. The relative density (20 / 4 ° C) 1.0889, flash point (open cup) 180 ° C and 193 ° C to ignite, melting 183.4kJ/mol hot, burning hot 3615kJ/mol. It is also widely used in polyester and polyurethane foam production, but also for alkyd coatings, synthetic lubricants, plasticizers, surfactants, rosin esters and the manufacture of explosives. Auxiliaries also directly used for PVC resin and the thermal stability of the alkyd resin applications can enhance the solid resin, color, weatherability, resistance to the chemical nature, sealing.

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How to Buy Methyl vegetable oil acid ester

Methyl vegetable oil acid ester  is light yellow oil liquid. The saponification value is 185-195mgKOH/g . It is also used in organic synthesis, auxiliary for light textile, oil product additives etc. It is good natural fatty acid methyl ester which are widely used in cosmetics and detergent and armoa and fragrance etc.
The transesterification of vegetable oil with short-chain alcohols, in the presence of base-catalyst, by means of low frequency ultrasound (28 and 40 kHz) in order to obtain biodiesel fuel was studied. By using ultrasounds the reaction time is much shorter (10-40 min) than for mechanical stirring. This decreased lubricity poses a significant problem as it may lead to wear and damage of diesel engines, primarily fuel injection systems. The quantity of required catalyst is 2 or 3 times lower. The molar ratio of alcohol/oil used is only 6:1. Normal chain alcohols react fast, while secondary and tertiary alcohols show some or no conversion after 60 min of reaction.
Previous studies on castor oil suggest that its uniquely high level of the hydroxy fatty acid ricinoleic acid may impart increased lubricity to the oil and its derivatives as compared to other vegetable oils.  Surprisingly, 40 kHz ultrasounds are much more effective in the reduction of the reaction time (10-20 min). Twenty eight kilohertz give slightly better yields (98-99%), but longer reaction time, while higher frequencies are not useful at all for the transesterification of fatty acids. (C) 2004 Elsevier B.V. All rights reserved.
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What is Mixed Methyl fatty acid ester

Mixed Methyl fatty acid ester is a light yellow oil liquid with the  saponification value 175-200mgKOH/g and the iodine value 80-110gI2/100g(MAX). The present invention utilizes the vegetable oil leftover as one waste from vegetable oil extraction in producing useful mixed fatty acid methyl ester, and can save resource and prevent environmental pollution. Fatty acids with conjugated double bonds have attracted great interest because of their reported potent bioactivities. However, there are currently no rapid methods for their structural characterization.
Mixed Methyl fatty acid ester is usually used in organic synthesis etc. The technological process of producing mixed fatty acid methyl ester with vegetable oil leftover includes the steps of dilution, cracking, steam stripping and hydrolysis, esterification, washing and distillation.
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How to Buy Animal oleic acid

Animal oleic acid is made from animal fat or plant oil, Main Uses:plastic, culture and education, tannage, medicine, washing, ore dressing , cosmetics , emulsifier , textile auxiliary , chemical auxiliary. It occurs as a light yellow or yellow brown transparent oily liquid, nontoxic. It’s commonly used as a replacement for animal fat sources that are high in saturated fat.
Chemical properties: Under normal temperature for light yellow transparent oily shape liquid, melting point, centigrade 134 0.8905 proportion, insoluble in water, soluble in ethanol, such as gasoline organic solvent, hydrogenated when into stearic acid, organic acid with the general chemical properties and unsaturated double bond of chemical properties.
Oleic acid is a monounsaturated fatty acid found naturally in many plant sources and in animal products. It is an omega-nine fatty acid, and considered one of the healthier sources of fat in the diet. It is widely used in the industries including textile, chemical, medicine, leather-making, stationary, rolling lubricant, re dressing and paper making etc..

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How to Get Capric acid

Carboxylic acid is an organic compound whose molecules contain carboxyl group and have the condensed chemical formula R-C(=O)-OH in which a carbon atom is bonded to an oxygen atom by a solid bond and to a hydroxyl group by a single bond), where R is a hydrogen atom, an alkyl group, or an aryl group. Capric acid is a white crystal with nasty smell.The melting point is 31.5℃ and the boiling point is 270℃，148-150℃(1.46kPa). It is soluble in alcohol, ether, benzene, chloroform and carbon disulfide, but insoluble in water. Molecular Weight: 172.27g/mol.
 Carboxylic acids can be synthesized if aldehyde is oxidized. Aldehyde can be obtained by oxidation of primary alcohol. Accordingly, carboxylic acid can be obtained by complete oxidation of primary alcohol. Molecular fomular: C10H20O2. It is one of three similar acids whose names are derived from the Latin word caper, meaning goat. Caproic (C6), caprylic (C8), and capric (C10) acids are present in significantly higher proportions in goat milk than in cow milk and are responsible for the characteristic goat-like smell that goat milk can develop. A variety of Carboxylic acids are abundant in nature and many carboxylic acids have their own trivial names. Examples are shown in table. It is also used in perfume,wetting agents, plasticizers, and food additives. In substitutive nomenclature, their names are formed by adding -oic acid' as the suffix to the name of the parent compound. The first character of carboxylic acid is acidity due to dissociation into H+ cations and RCOO- anions in aqueous solution. It is used in preparation for decanoate products.
Manufacturing of esters for artificial fruit flavors and perfumes. Also as an intermediate in chemical syntheses. CAS: 334-48-5. The almost infinite esters provide a wide range of viscosity, specific gravity, vapor pressure, boiling point, and other physical and chemical properties for the proper application selections.
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How to Get Capric acid

Carboxylic acid is an organic compound whose molecules contain carboxyl group and have the condensed chemical formula R-C(=O)-OH in which a carbon atom is bonded to an oxygen atom by a solid bond and to a hydroxyl group by a single bond), where R is a hydrogen atom, an alkyl group, or an aryl group. Capric acid is a white crystal with nasty smell.The melting point is 31.5℃ and the boiling point is 270℃，148-150℃(1.46kPa). It is soluble in alcohol, ether, benzene, chloroform and carbon disulfide, but insoluble in water. Molecular Weight: 172.27g/mol.
 Carboxylic acids can be synthesized if aldehyde is oxidized. Aldehyde can be obtained by oxidation of primary alcohol. Accordingly, carboxylic acid can be obtained by complete oxidation of primary alcohol. Molecular fomular: C10H20O2. It is one of three similar acids whose names are derived from the Latin word caper, meaning goat. Caproic (C6), caprylic (C8), and capric (C10) acids are present in significantly higher proportions in goat milk than in cow milk and are responsible for the characteristic goat-like smell that goat milk can develop. A variety of Carboxylic acids are abundant in nature and many carboxylic acids have their own trivial names. Examples are shown in table. It is also used in perfume,wetting agents, plasticizers, and food additives. In substitutive nomenclature, their names are formed by adding -oic acid' as the suffix to the name of the parent compound. The first character of carboxylic acid is acidity due to dissociation into H+ cations and RCOO- anions in aqueous solution. It is used in preparation for decanoate products.
Manufacturing of esters for artificial fruit flavors and perfumes. Also as an intermediate in chemical syntheses. CAS: 334-48-5. The almost infinite esters provide a wide range of viscosity, specific gravity, vapor pressure, boiling point, and other physical and chemical properties for the proper application selections.
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Lauric acid for Sale

Lauric acid is a colorless, needle-like crystals with slight odor of bay oil. It is insoluble in water. Containers of this material may be hazardous when empty since they retain product residues (dust, solids); observe all warnings and precautions listed for the product. The melting point is 44 - 46C (111 - 115F) and the boiling point is 225C (437F) @ 100mm. Thus, it is often used in laboratory investigations of freezing-point depression. Like many other fatty acids, lauric acid is inexpensive, has a long shelf-life, and is non-toxic and safe to handle.
Lauric acid (systematically: dodecanoic acid), a saturated fatty acid, is a white, powdery solid with a faint odor of bay oil or soap. Lauric acid is inexpensive, has a long shelf-life, and is non-toxic and safe to handle. Protect against physical damage. Isolate from incompatible substances. It is mainly used for the production of soaps and cosmetics. For these purposes, lauric acid is neutralized with sodium hydroxide to give sodium laurate, which is a soap. Lauric acid is a medium chain fatty acid, which has the additional beneficial function of being formed into monolaurin in the human or animal body.
Lauric acid is a solid at room temperature but melts easily in boiling water, so liquid lauric acid can be treated with various solutes and used to determine their molecular masses. This product should be keept in a tightly closed container, stored in a cool, dry, ventilated area. Most commonly, sodium laurate is obtained by saponification of various oils, such as coconut oil.
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