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List of compounds with carbon number 21; List of compounds with carbon number 22; List of compounds with carbon number 23; List of compounds with carbon number 24; List of compounds with carbon numbers 25-29; List of compounds with carbon numbers 30-39; List of compounds with carbon numbers 40-49; List of compounds with carbon numbers 50+
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Of most concern are the family of chemicals called VOCs such as formaldehyde, toluene, and limonene. [7] Volatile organic compounds (VOCs) are released from many household cleaning products such as disinfectants, polishes, floor waxes, air-freshening sprays, all-purpose cleaning sprays, and glass cleaner. These products have been shown to emit ...
An ester of carboxylic acid.R stands for any group (organic or inorganic) and R′ stands for organyl group.. In chemistry, an ester is a compound derived from an acid (organic or inorganic) in which the hydrogen atom (H) of at least one acidic hydroxyl group (−OH) of that acid is replaced by an organyl group (−R).
In almost all known compounds, bismuth has oxidation state +3; a few have states +5 or −3. The trioxide [25] [48] and trisulfide can both be made from the elements, [49] [36] although the trioxide is extremely corrosive at high temperatures. [37] The pentoxide is not stable at room temperature, and will evolve O 2 gas if heated. [50]
May have antibiotic effects in some compounds when it substitutes for chlorine. [24] Bromine compounds are very common in and presumably essential to a variety of marine organisms, including bacteria, fungi, seaweeds, and diatoms. [25] [26] Most marine organobromine compounds are made by the action of a unique algal enzyme, vanadium ...
The MCL for PFOA and PFOS, two of the most common compounds, is 4 parts per trillion. Four other PFAS compounds — PFNA, PFHxS, PFBS and Gen X chemicals — each of an MCL of 10 ppt.
Halogenating a hydrocarbon produces something that is not a hydrocarbon. It is a very common and useful process. Hydrocarbons with the same molecular formula but different structural formulae are called structural isomers. [1]: 625 As given in the example of 3-methylhexane and its higher homologues, branched hydrocarbons can be chiral.