| Anmol Chemicals is the pioneer manufacturers of White Beeswax, Pharmaceutical Excipients Fragrance Food Food & Flavor chemicals in India. We supply Halal and Kosher White Beeswax made in an ISO9001, ISO22000 (FSSC22000) cGMP and GLP certified facility. Our group has several manufacturing facilities spread across the world, supported by toll manufacturers and representatives in UAE, Europe, USA, China and has several associated manufacturing facilities spread across India. All the Information on Physics, Chemistry, Applications, Uses and Technology on Manufacture of White Beeswax is in these pages. |
| The units have one or more of the certifications like FDA GMP, ISO 9001, ISO 22000, HACCP, REACH, Kosher & Halal |
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White Beeswax BP Ph Eur Grade Manufacturers
White Beeswax SDS MSDS Sheet of Manufacturers
White Beeswax BP Ph Eur Manufacturers. YOU ARE HERE.
White Beeswax FCC Food Grade Manufacturers
White Beeswax BP Ph Eur Grade
Action and use: Excipient.
DEFINITION
Wax obtained by bleaching yellow beeswax.
CHARACTERS
Appearance: White or yellowish-white pieces or plates, translucent when thin, with a fine-grained, matt and non-crystalline fracture; when warmed in the hand they become soft and malleable. It has an odour similar to that of yellow beeswax, though fainter and never rancid. It is tasteless and does not stick to the teeth.
Solubility: Practically insoluble in water, partially soluble in hot ethanol (90 per cent V/V) and completely soluble in fatty and essential oils.
Relative density: About 0.960.
TESTS
Drop point: 61C to 66C.
Melt the beeswax by heating on a water-bath, pour onto a glass plate and allow to cool to a semi-solid mass. Fill the metal cup by inserting the wider end into the beeswax and repeating the procedure until beeswax extrudes from the narrow opening. Remove the excess with a spatula and insert the thermometer immediately. Remove the beeswax displaced. Allow to stand at room temperature for at least 12 h before determining the drop point.
Acid value: 17.0 to 24.0.
To 2.00 g (m g), in a 250 ml conical flask fitted with a reflux condenser, add 40 ml of xylene and a few glass beads. Heat until the substance is dissolved. Add 20 ml of ethanol (96 percent) and 0.5 ml of phenolphthalein solution and titrate the hot solution with 0.5 M alcoholic potassium hydroxide until a red colour persists for at least 10 s (n1 ml). Carry out a blank test (n2 ml).
Ester value: 70 to 80.
Saponification value: 87 to 104.
To 2.00 g (m g), in a 250 ml conical flask fitted with a reflux condenser, add 30 ml of a mixture of equal volumes of ethanol (96 per cent) and xylene and a few glass beads. Heat until the substance is dissolved. Add 25.0 ml of 0.5 M alcoholic potassium hydroxide and heat under a reflux condenser for 3 h. Titrate the hot solution immediately with 0.5 M hydrochloric acid , using 1 ml of phenolphthalein solution as indicator (n1 ml). Reheat the solution to boiling several times during the course of the titration. Carry out a blank test (n2 ml).
Ceresin, paraffins and certain other waxes: To 3.0 g, in a 100 ml round-bottomed flask, add 30 ml of a 40 g/l solution of potassium hydroxide in aldehyde-free alcohol and boil gently under a reflux condenser for 2 h. Remove the condenser and immediately insert a thermometer. Place the flask in a water-bath at 80C and allow to cool, swirling the solution continuously. No precipitate is formed until 65C, although the solution may be slightly opalescent. Beginning at 65C, the solution may become cloudy and precipitates may be formed. At 59C, the solution is cloudy.
Glycerol and other polyols: Maximum 0.5 per cent m/m, calculated as glycerol.
To 0.20 g add 10 ml of alcoholic potassium hydroxide solution and heat on a water-bath under a reflux condenser for 30 min. Add 50 ml of dilute sulphuric acid, cool and filter. Rinse the flask and the filter with dilute sulphuric acid. Combine the filtrate and washings and dilute to 100.0 ml with dilute sulphuric acid. Place 1.0 ml of the solution in a test-tube, add 0.5 ml of a 10.7 g/l solution of sodium periodate, mix and allow to stand for 5 min. Add 1.0 ml of decolorised fuchsin solution and mix. Any precipitate disappears. Place the tube in a beaker containing water at 40C. During cooling observe for 10-15 min. Any violet-blue colour in the solution is not more intense than that in a standard prepared at the same time and in the same manner using 1.0 ml of a 10 mg/l solution of glycerol R in dilute sulphuric acid.
Manufacturers
Anmol Chemicals
S-8, SARIFA MANSION, 2ND FLANK ROAD, CHINCHBUNDER, MUMBAI 400009, INDIA
TEL: (OFFICE) 91-22-23770100, 23726950, 23774610, 23723564. FAX: 91-22-23728264
e-mail: anmolc@mtnl.net.in
Exports to USA, Canada, UAE, Dubai, South Africa, Tanzania, Kenya, Nigeria, Egypt, Uganda, Turkey, Mexico, Brazil, Chile, Argentina, Europe Netherlands, Italy, Spain, Germany, Portugal, France, Malaysia, Indonesia, Thailand, Russia, Norway, Korea, Japan, etc.
Copyright and Usual Disclaimer is Applicable. 23 February, 2022
Barter
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Yet my love for you keeps waiting for you