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2. USG Corporation - Wikipedia

   en.wikipedia.org/wiki/USG_Corporation

   US$1.89 billion (2016) Number of employees. 6,800 [1] (2017) Parent. Knauf. Website. www .usg .com. USG Corporation, also known as United States Gypsum Corporation, is an American company which manufactures construction materials, most notably drywall and joint compound. The company is the largest distributor of wallboard in the United States ...

3. Joint compound - Wikipedia

   en.wikipedia.org/wiki/Joint_compound

   Joint compound is used to finish gypsum panel joints filled with paper or fiber joint tape, corner bead, trim and fasteners, and to skim coat. It is also convenient for patching holes, bumps, tears, and other minor damage to existing walls. In North America, troweling joint mud on gypsum panels is a standard construction technique prior to ...

4. Safety data sheet - Wikipedia

   en.wikipedia.org/wiki/Safety_data_sheet

   A safety data sheet ( SDS ), [1] material safety data sheet ( MSDS ), or product safety data sheet ( PSDS) is a document that lists information relating to occupational safety and health for the use of various substances and products. SDSs are a widely used type of fact sheet used to catalogue information on chemical species including chemical ...

5. Talk:Joint compound - Wikipedia

   en.wikipedia.org/wiki/Talk:Joint_compound

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6. SDS-PAGE - Wikipedia

   en.wikipedia.org/wiki/SDS-PAGE

   SDS-PAGE ( sodium dodecyl sulfate–polyacrylamide gel electrophoresis) is a discontinuous electrophoretic system developed by Ulrich K. Laemmli which is commonly used as a method to separate proteins with molecular masses between 5 and 250 kDa. [1] [2] The combined use of sodium dodecyl sulfate (SDS, also known as sodium lauryl sulfate) and ...

7. Dechlorane plus - Wikipedia

   en.wikipedia.org/wiki/Dechlorane_plus

   Dechlorane plus (abbrev. DDC-CO [1]) is a polychlorinated flame retardant produced by Oxychem. Its log P is 11.27±0.94. [2] It is produced by the Diels-Alder reaction of two equivalents of hexachlorocyclopentadiene with one equivalent of cyclooctadiene. The syn and anti isomer are formed in the approximate ratio of 1:3.