LABORATORY CHEMICALS

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Keeping in view the altering demands of our customers, we are indulged in offering Acetic Acid.
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Highly effective
Perfectly prepared
Safe packing
Exact preparation
Elevated shelf life
Reliable
 
Product Price:
Acetic Acid: 23.75 Rs.+excise +tax (tanker load) per kg for Mumbai
 

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This compound is used as a solvent to dissolve cellulose ethers, lacquers, resins, fats, waxes, oils, bitumen and crude rubber. It is also used in perfume manufacturing, during surface coating operations (lacquers), in synthesis of adipic acid for production of nylon 66 and engineering plastics, during synthesis of caprolactam in nylon 6, paint and varnish remover, in the extraction of essential oils, in analytical chemistry for molecular weight determinations, in the manufacturing of adipic acid, benzene, cyclohexyl chloride, nitrocyclohexane, cyclohexanol and cyclohexanone, in the manufacturing of solid fuel for camp stoves, in fungicidal formulations (possesses slight fungicidal action) in the industrial recrystallising of steroids, organic synthesis, recrystallising medium glass substitutes, solid fuels, in analytical chemistry and in manufacturing of adhesives.

Substance details

Substance name: Cyclohexane

CASR number: 110-82-7

Molecular formula: C6H12

Synonyms: hexamethylene; hexanaphthene; hexahydrobenzene, benzenehexahydride 

Physical properties

Cyclohexane is a colourless, mobile liquid with a mild, sweet odour. It is slightly soluble in water and soluble in alcohol, acetone, benzene, ethanol, ethyl ether, olive oil, and carbon tetrachloride.

Melting Point: 6.47°C

Boiling Point: 80.7°C

Specific Gravity: 0.779

Vapour Density: 2.98

1 ppm = 3.44 mg/m3

Formula weight 84.161

Chemical properties

Cyclohexane is a flammable, non-corrosive liquid.

Further information

The National Pollutant Inventory (NPI) holds data for all sources of cyclohexane emissions in Australia.

• Australia's cyclohexane emission report

Description

Effects of cyclohexane on human health and the environment depend on how much cyclohexane is present and the length and frequency of exposure. Effects also depend on the health of a person or the condition of the environment when exposure occurs. Breathing large amounts of cyclohexane for short periods of time adversely affects the human nervous system. Effects range from headaches to anaesthesia, tremors, and convulsions. Contact with cyclohexane liquid or vapour can damage the eyes. These effects are not likely to occur at levels of cyclohexane that are normally found in the environment. Human health effects associated with breathing or otherwise consuming smaller amounts of cyclohexane over long periods of time are not known. Studies show that repeat exposure to large amounts of cyclohexane in air causes nervous system effects, eye damage, and respiratory effects in animals. The cyclohexane industry is now studying how its chemical affects the reproductive system and the development of the foetus of animals.

Entering the body

Cyclohexane enters the body when breathed in with contaminated air or when consumed with contaminated food or water. It can also be absorbed through skin contact. Cyclohexane is not likely to remain in the body due to its breakdown and removal in exhaled air and in urine.

Exposure

Exposure to cyclohexane can occur in the workplace or in the environment following releases to air, water, land, or groundwater. Exposure can also occur when people use products that contain cyclohexane or when they smoke cigarettes.

Workplace exposure standards

Safe Work Australia sets the workplace exposure standard for cyclohexane through the workplace exposure standards for airborne contaminants:

• Maximum eight hour time weighted average (TWA): 100 parts per million (350 mg/m3)
• Maximum short term exposure limit (STEL): 300 parts per million (1050 mg/m3)

These standards are only appropriate for use in workplaces and are not limited to any specific industry or operation. Make sure you understand how to interpret the standards before you use them.

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• Production Capacity: As per customer requirement
• Delivery Time: 1-2Days
• Packaging Details: Tanker load from Mumbai, Hazira & Kandla port.

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FormLiquid

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We are offering our clients premium quality Hydrogen Peroxide (H2O2), that is processed using high grade chemical and various other basic ingredient as per the set industry norms.

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Nonylphenols are a family of closely related organic compounds called alkylphenols. They are used in manufacturing antioxidants, lubricating oil additives, laundry and dish detergents, emulsifiers, and solubilizers.

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So as to attain enormous level of customer trust and credibility, we have been instrumental in rendering Acrylic Acid.
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Effective
Longer shelf life
Reliable
Perfect formulation
Hugely demanded
Balanced pH value

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• Pay Mode Terms: T/T (Bank Transfer)

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Perchloroethylene is a colorless, nonflammable liquid with a sweet, ether-like odor. It is also called tetrachloroethylene, PCE, or PERC. The chemical formula for perchloroethylene is C₂Cl₄.Perchloroethylene is a volatile organic compound (VOC).

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• Pay Mode Terms: T/T (Bank Transfer)
• Port of Dispatch: Mumbai

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Isobutanol (IUPAC nomenclature: 2-methylpropan-1-ol) is an organic compound with the formula (CH₃)₂CHCH₂OH (sometimes represented as i-BuOH). This colorless, flammable liquid with a characteristic smell is mainly used as a solvent either directly or as its esters. Its isomers are 1-butanol, 2-butanol, and tert-butanol, all of which are important industrially.^[5]

Production[edit]

Isobutanol is produced by the carbonylation of propylene. Two methods are practiced industrially, hydroformylation is more common and generates a mixture of isobutyraldehyde and butyraldehyde:

CH₃CH=CH₂ + CO + H₂ → CH₃CH₂CH₂CHO

The reaction is catalyzed by cobalt or rhodium complexes. The resulting aldehydes are hydrogenated to the alcohols, which are then separated. In Reppe carbonylation, the same products are obtained, but the hydrogenation is effected by the water-gas shift reaction.^[5]

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• Production Capacity: As per customer requirement
• Delivery Time: 1-2Days
• Packaging Details: Available in tanker from Mumbai & Kandla port.

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We are reckoned amongst the clients for offering the best quality (tested) of Caustic Potash.

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Product Description:
Grade
Technical
Form
Solid
Other Trade Name
Carbolic Acid
Chemical Formula
C6H5OH
Product Description
Clear Colourless liquid
Spec. No.
PHE/2010-2011
CAS No
108-95-2
UN No.
1671

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• Delivery Time: 1/2 days
• Packaging Details: 200kgs drums

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Product Specification Product Number: C40200 CAS Number: 870-24-6 MDL: MFCD00012887 Formula: C2H6ClN · HCl Formula Weight: 115.99 g/mol TEST Specification ________________________________________________________________________ Appearance (Color) White to Off White Appearance (Form) Powder or Crystal or Chunk(s) Infrared spectrum Conforms to Structure Titration by AgNO3 98.5 - 101.5 % GC (area %) > 98.5 %

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• Item Code: 29211990
• Delivery Time: 1-2days
• Packaging Details: 25Kgs & 50Kgs Carbouy

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Titanium dioxide, also known as titanium(IV) oxide or titania, is the naturally occurring oxide oftitanium, chemical formula TiO.

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• Pay Mode Terms: T/T (Bank Transfer)
• Port of Dispatch: Mumbai

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Formula: Sb₂O₃Molar mass: 291.52 g/molMelting point: 656 °CDensity: 5.2 g/cm³Boiling point: 1,425 °C

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• Item Code: 28258000
• Pay Mode Terms: T/T (Bank Transfer),Other
• Port of Dispatch: EX BHIWANDI
• Delivery Time: WITHIN 2 DAYS FROM THE ORDER DATE
• Packaging Details: 25 KGS

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Hydroquinone, also known as benzene-1,4-diol or quinol, is an aromatic organic compound that is a type of phenol, a derivative of benzene, having the chemical formula C₆H₄(OH)₂. It has two hydroxyl groups bonded to a benzene ring in a para position. It is a white granular solid. Substituted derivatives of this parent compound are also referred to as hydroquinones. The name "hydroquinone" was coined by Friedrich Wöhler in 1843.^[7]

Production[edit]

Hydroquinone is produced industrially in two main ways.^[8]

• The most widely used route is similar to the cumene process in reaction mechanism and involves the dialkylation of benzene with propene to give 1,4-diisopropylbenzene. This compound reacts with air to afford the bis(hydroperoxide), which is structurally similar to cumene hydroperoxide and rearranges in acid to give acetone and hydroquinone.^[9]
• A second route involves hydroxylation of phenol over a catalyst. The conversion uses hydrogen peroxide and affords a mixture of hydroquinone and its ortho isomer catechol (benzene-1,2-diol):C6H5OH+H2O2⟶C6H4(OH)2+H2O

Other, less common methods include:

• A potentially significant synthesis of hydroquinone from acetylene and iron pentacarbonyl has been proposed^{[10][11][12][13][14][15]} Iron pentacarbonyl serves as a catalyst, rather than as a reagent, in the presence of free carbon monoxide gas. Rhodium or ruthenium can substitute for iron as the catalyst with favorable chemical yields but are not typically used due to their cost of recovery from the reaction mixture.^[10]
• Hydroquinone and its derivatives can also be prepared by oxidation of various phenols. Examples include Elbs persulfate oxidation and Dakin oxidation.
• Hydroquinone was first obtained in 1820 by the French chemists Pelletier and Caventou via the dry distillation of quinic acid.^[16]