Solvent

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Benzyl alcohol is used as a bacteriostatic preservative at low concentration in intravenous medications, cosmetics and topical drugs. The use of benzyl alcohol as a 5% solution has been approved by the U.S. FDA for the treatment of head lice in children older than 6 months and in adults.

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Diethylene glycol is used in the manufacture of unsaturated polyester resins, polyurethanes, and plasticizers. DEG is used as a building block in organic synthesis, e.g. of morpholine and 1,4-dioxane. It is a solvent for nitrocellulose, resins, dyes, oils, and other organic compounds.

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The compound is classified as heterocyclic compound, specifically a cyclic ether. It is a colorless, water-miscible organic liquid with low viscosity. It is mainly used as a precursor to polymers. Being polar and having a wide liquid range, THF is a versatile solvent.

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Butyl Cellosolve (Butyl Glycol) cellThis colorless liquid has a sweet, ether-like odor, as it derives from the family of glycol ethers, and is a butyl ether of ethylene glycol. As a relatively nonvolatile, inexpensive solvent of low toxicity, it is used in many domestic and industrial products because of its properties as a surfactant.

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Methyl acetoacetate is used as a chemical reagent used in the synthesis of pharmaceuticals.

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2 Ethylhexanol Price List


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2 E.H ( OCTANOL ) is used such as or as a raw material in various applications: flavors and fragrances, paints and coatings, inks, adhesives, home care, lubricants and fuels. 2-Octanol can be a biobased alternative of 2-ethylhexanol and its derivates in numerous applications. Get Best price of >99% pure 25 litres can of 2 Ethylhexanol CAS No. 104-76-7, C8H18O. For Certificate of Analysis (COA) & MSDS, kindly contact us.

2-Ethylhexanol (abbreviated 2-EH) is a branched, eight-carbon chiral alcohol. It is a colorless liquid that is poorly soluble in water but soluble in most organic solvents. It is produced on a massive scale (>2,000,000,000 kg/y) for use in numerous applications such as solvents. It is encountered in natural plant fragrances, and the odor has been reported as "heavy, earthy, and slightly floral" for the R enantiomer and "a light, sweet floral fragrance" for the S enantiomer

Uses:

• Used in solvents
• Used as flavouring agents
• Used in fragrances
• As a precursor for plasticizers

Hazards:

• It has low toxicity
• Causes respiratory tract irritation
• Harmful if swallowed
• Inhalation of vapours is harmful

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Iso Propyl Alcohol Price List

Get Best price of >99% pure 25 litre bottle of Isopropyl Alcohol CAS No. 63-67-0, C3H8O. For Certificate of Analysis (COA) & MSDS, kindly contact us.

Uses:

• Used in paint industry
• Used for making perfumes
• Pharmaceutical applications
• lacquer formulations, dye solutions, antifreezes, soaps, window cleaners
• Used for making sanitizers
• Major component in household cleaners

Isopropyl alcohol (IUPAC name propan-2-ol; also called isopropyl, isopropanol, or 2-propanol) is a colorless, flammable chemical compound (chemical formula CH3CHOHCH3) with a strong odor. As an isopropyl group linked to a hydroxyl group, it is the simplest example of a secondary alcohol, where the alcohol carbon atom is attached to two other carbon atoms. It is a structural isomer of 1-propanol and ethyl methyl ether. Isopropyl Alcohol is an isomer of propyl alcohol with antibacterial properties.

Isopropyl alcohol, particularly in solutions between 60% and 90% alcohol with 10 – 40% purified water, is rapidly antimicrobial against bacteria, fungi, and viruses. Once alcohol concentrations drop below 50%, usefulness for disinfection drops sharply. Notably, higher concentrations of alcohol don’t generate more desirable bactericidal, virucidal, or fungicidal properties. Alcohol-based versions typically contain some combination of isopropyl alcohol, ethanol (ethyl alcohol), or n-propanol, with versions containing 60% to 95% alcohol the most effective. Care should be taken as they are flammable. Alcohol-based hand sanitizer works against a wide variety of microorganisms but not spores. Compounds such as glycerol may be added to prevent drying of the skin. Some versions contain fragrances; however, these are discouraged due to the risk of allergic reactions. Non-alcohol based versions typically contain benzalkonium chloride or triclosan; but are less effective than alcohol-based ones.
Isopropyl alcohol is effective against viruses such as FCV at 40% – 60% concentrations. Ethanol however, is more effective at 70% – 90% concentrations against FCV. In other cases, isopropyl alcohol is more effective than ethanol at lower percentage concentrations.

Methods of Manufacturing:
Indirect hydration process is based on a two-step reaction of propylene and sulfuric acid; in the first step, mixed sulfate esters, primarily isopropyl hydrogen sulfate, but also diisopropyl sulfate, form; these are then hydrolyzed, forming isopropanol and sulfuric acid.

Health Hazards:
Vapors cause mild irritation of eyes and upper respiratory tract; high concentrations may be anesthetic. Liquid irritates eyes and may cause injury; harmless to skin; if ingested causes drunkenness and vomiting.

Fire Hazards:
Highly flammable. Vapour/air mixtures are explosive. Risk of explosion on contact with strong oxidants. 

First Aid:
EYES: First check the victim for contact lenses and remove if present. Flush victim's eyes with water or normal saline solution for 20 to 30 minutes while simultaneously calling a hospital or poison control center. Do not put any ointments, oils, or medication in the victim's eyes without specific instructions from a physician.

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Methylene chloride is used in paint and varnish remover formulations, solvent vapor depressent in aerosol applications, general cleaning solvent and as a foam blowing agent for flexible polyurethane foams. It is also called as Dichloromethane.

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Formaldehyde is a colorless, flammable, strong-smelling chemical widely used by industry to make home building products. It is a colorless gas at room temperature, or available as a liquid called formalin. Formaldehyde is widely used to manufacture building materials and household products.

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Xylene - It is primarily used as a solvent (a liquid that can dissolve other substances) in the printing, rubber, and leather industries. Along with other solvents, xylene is also widely used as a cleaning agent, a thinner for paint, and in varnishes.

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n-Butanol or n-butyl alcohol or normal butanol is a primary alcohol with a 4-carbon structure and the chemical formula C₄H₉OH. Its isomers include isobutanol, 2-butanol, and tert-butanol. Butanol is one of the group of "fusel alcohols" (from the German for "bad liquor"), which have more than two carbon atoms and have significant solubility in water.^[6]

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Benzene is used mainly as an intermediate to make other chemicals, above all ethylbenzene, cumene, cyclohexane, nitrobenzene, and alkylbenzene. More than half of the entire benzene production is processed into ethylbenzene, a precursor to styrene, which is used to make polymers and plastics like polystyrene and EPS. Some 20% of the benzene production is used to manufacture cumene, which is needed to produce phenol and acetone for resins and adhesives. Cyclohexane consumes c.

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• Item Code: 71-43-2
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monomers it can be used to prepare various copolymers such as ethylene-vinyl acetate (EVA), vinyl acetate-acrylic acid (VA/AA), polyvinyl chloride acetate (PVCA), and polyvinylpyrrolidone (Vp/Va Copolymer, used in hair gels.

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DMSO is frequently used as a solvent for chemical reactions involving salts, most notably Finkelstein reactions and other nucleophilic substitutions. It is also extensively used as an extractant in biochemistry and cell biology.^[9]Because DMSO is only weakly acidic, it tolerates relatively strong bases and as such has been extensively used in the study of carbanions.

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• Item Code: 67-68-5
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The racemic 2-ethylhexyl acrylate can be prepared with a high yield by esterification of acrylic acid with racemic 2-ethylhexanol in the presence of hydroquinone as a polymerization inhibitor and a strong acid such as methanesulfonic acid by reactive distillation using toluene as azeotroping agent.^[1]

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which used to make polycarbonate plastic and 21% going into epoxy resins.^[9] In the  less than 5% of the BPA produced is used in food contact applications,^[10] but remains in the canned food industry and printing applications such as sales receipts.

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hexanes are used in the formulation of glues for shoes, leather products, and roofing. They are also used to extract cooking oils (such as canola oil or soy oil) from seeds, for cleansing and degreasing a variety of items, and in textile manufacturing. They are commonly used in food based soybean oil extraction in the United States, and are potentially present as contaminants in all soy food products in which the technique is used; the lack of regulation by the FDA of this contaminant is a matter of some controversy.

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• Item Code: 110-54-3
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Nonylphenol is used in manufacturing antioxidants, lubricating oil additives, laundry and dish detergents, emulsifiers, and solubilizers.^[2] It can also be used to produce tris(4-nonyl-phenyl) phosphite (TNPP), which is an antioxidant used to protect polymers, such as rubber, Vinyl polymers, polyolefins, and polystyrenics in addition to being a stabilizer in plastic food packaging. Barium and calcium salts of nonylphenol are also used as heat stabilizers for polyvinyl chloride (PVC).^[15] Nonylphenol is also often used an intermediate in the manufacture of the non-ionic surfactants nonylphenol exthoxylates, which are used in detergents, paints, pesticides, personal care products, and plastics.

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2 MERCAPTOETHANOL is commonly abbreviated, is used to reduce disulfide bonds and can act as a biological antioxidant by scavenging hydroxyl radicals (amongst others). It is widely used because the hydroxyl group confers solubility in water and lowers the volatility. Due to its diminished vapor pressure, its odor, while unpleasant, is less objectionable than related thiols.

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Ethylene dichloride (EDC), is a chlorinated hydrocarbon, mainly used to produce vinyl chloride monomer (VCM, chloroethene), the major precursor for PVC production. It is a colorless liquid with a chloroform-like odor.It is a precursor to TCE which is used in dry cleaning.It was used as degreaser and paint remover and as an anti knock additive in leaded fuels to scavenge lead from cylinders and valves preventing buildup.As a useful building block reagent it is used in making ethylene diamine and in laboratory used as a source of chlorine.

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Chloroform, or trichloromethane, is an organic compound with formula CHCl₃. It is a colorless, sweet-smelling, dense liquid that is produced on a large scale as a precursor to PTFE.

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2-Ethylhexanoic acid is the organic compound. It is a carboxylic acid that is widely used to prepare lipophilic metal derivatives that are soluble in nonpolar organic solvents. 2-Ethylhexanoic acid is a colorless viscous oil.They fare used as catalyst in polymerizations as well as for oxidation reactions as oil drying agents.

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coli has the capacity to use lignocellulose (waste plant matter left over from agriculture) in the synthesis of isobutanol. The use of lignocellulose prevents E. coli from using plant matter meant for human consumption, and prevents any food-fuel price relationship which would occur from the biosynthesis of isobutanol by E. coli.
Genetic modification has been used to broaden the scope of lignocellulose which can be used by E. coli. This has made E. coli a useful and diverse isobutanol bio-synthesizer. Get Best price of >99% pure 200 litre drum of Isobutanol CAS No. 78-83-1, C4H10O. It is used in printing inks, manufacturing of coating resins & paint thinners.

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Other uses include rubber processing chemicals (9%), herbicides (2%), and dyes and pigments (2%). As additives to rubber, aniline derivatives such as phenylenediamines and diphenylamine, are antioxidants. Illustrative of the drugs prepared from aniline is paracetamol (acetaminophen, Tylenol).

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Ethyl acetoacetate is often used in the acetoacetic ester synthesis similar to diethyl malonate in the malonic ester synthesis or the Knoevenagel condensation. The protons alpha to carbonyl groups are acidic, and the resulting carbanion can undergo nucleophilic substitution. A subsequent thermal decarboxylation is also possible.

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