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  2. Ethylene glycol - Wikipedia

    en.wikipedia.org/wiki/Ethylene_glycol

    Ethylene glycol may also be one of the minor ingredients in screen cleaning solutions, along with the main ingredient isopropyl alcohol. Ethylene glycol is commonly used as a preservative for biological specimens, especially in secondary schools during dissection as a safer alternative to formaldehyde. It is also used as part of the water-based ...

  3. Ethylene glycol poisoning - Wikipedia

    en.wikipedia.org/wiki/Ethylene_glycol_poisoning

    These symptoms are a result of accumulation of organic acids formed by the metabolism of ethylene glycol. Additionally low calcium concentrations in the blood, overactive muscle reflexes, muscle spasms, QT interval prolongation, and congestive heart failure may occur. If untreated, death most commonly occurs during this period.

  4. Ethylene glycol (data page) - Wikipedia

    en.wikipedia.org/wiki/Ethylene_glycol_(data_page)

    Temperature dependence of ethylene glycol vapor pressure. Uses formula ...

  5. Diethylene glycol - Wikipedia

    en.wikipedia.org/wiki/Diethylene_glycol

    The resulting product is two ethylene glycol molecules joined by an ether bond. [5] "Diethylene glycol is derived as a co-product with ethylene glycol (MEG) and triethylene glycol. The industry generally operates to maximize MEG production. Ethylene glycol is by far the largest volume of the glycol products in a variety of applications.

  6. Chemical waste - Wikipedia

    en.wikipedia.org/wiki/Chemical_waste

    The U.S. Environmental Protection Agency (EPA) prohibits disposing of certain materials down drains. [4] Therefore, when hazardous chemical waste is generated in a laboratory setting, it is usually stored on-site in appropriate waste containers, such as triple-rinsed chemical storage containers [5] or carboys, where it is later collected and disposed of in order to meet safety, health, and ...

  7. Protecting group - Wikipedia

    en.wikipedia.org/wiki/Protecting_group

    Overall, trans-acetalation plays a lesser role in forming protective acetals; they are formed as a rule from glycols through dehydration. Normally a simple glycol like ethylene glycol or 1,3-propadiol is used for acetalation.Modern variants also use glycols, but with the hydroxyl hydrogens replaced with a trimethylsilyl group. [60] [61]

  8. Diol - Wikipedia

    en.wikipedia.org/wiki/Diol

    In a vicinal diol, the two hydroxyl groups occupy vicinal positions, that is, they are attached to adjacent atoms. These compounds are called glycols [5] (though the term can be used more widely). Examples include ethane-1,2-diol or ethylene glycol HO−(CH 2) 2 −OH, a common ingredient of antifreeze products.

  9. National Emissions Standards for Hazardous Air Pollutants

    en.wikipedia.org/wiki/National_Emissions...

    ^2 Includes mono- and di- ethers of ethylene glycol, diethylene glycol, and triethylene glycol R−(OCH 2 CH 2) n −OR' where; n = 1, 2, or 3 R = alkyl C7 (chain of 7 carbon atoms) or less; or phenyl or alkyl substituted phenyl R' = H or alkyl C7 or less; or OR' consisting of carboxylic acid ester, sulfate, phosphate, nitrate, or sulfonate.