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  2. 1-Chlorobutane - Wikipedia

    en.wikipedia.org/wiki/1-Chlorobutane

    1-Chlorobutane is an alkyl halide with the chemical formula CH 3 (CH 2) 3 Cl. It is a colorless, flammable liquid. It is a colorless, flammable liquid. Preparation and reactions

  3. Organosulfate - Wikipedia

    en.wikipedia.org/wiki/Organosulfate

    Alkyl sulfates if ingested are well-absorbed and are metabolized into a C 3, C 4 or C 5 sulfate and an additional metabolite. The highest irritant of the alkyl sulfates is sodium laurylsulfate, with the threshold before irritation at a concentration of 20%. Surfactants in consumer products are typically mixed, reducing likelihood of irritation.

  4. 1,4-Butane sultone - Wikipedia

    en.wikipedia.org/wiki/1,4-Butane_sultone

    1,4-butane sultone is a six-membered δ-sultone and the cyclic ester of 4-hydroxybutanesulfonic acid.As a sulfo-alkylating agent, 1,4-butanesultone is used to introduce the sulfobutyl group (–(CH 2) 4 –SO 3 −) into hydrophobic compounds possessing nucleophilic functional groups, for example hydroxy groups (as in the case of β-cyclodextrin [1]) or amino groups (as in the case of ...

  5. 1,4-Dichlorobutane - Wikipedia

    en.wikipedia.org/wiki/1,4-Dichlorobutane

    1,4-Dichlorobutane is a chloroalkane with the molecular formula (CH 2 CH 2 Cl) 2. It is one of several structural isomers of dichlorobutane. They are all colorless liquids of low flammabiltity and of interest for specialized synthetic uses.

  6. How to be a good cat owner in 2024: Top tips from a vet - AOL

    www.aol.com/good-cat-owner-2024-top-120000333.html

    Dr. MacMillan says: "Being a good cat owner means housing your cat in an appropriate environment, with a suitable temperature and noise level, natural light, and a comfortable resting space."

  7. Organochlorine chemistry - Wikipedia

    en.wikipedia.org/wiki/Organochlorine_chemistry

    Alkyl chlorides are versatile building blocks in organic chemistry. While alkyl bromides and iodides are more reactive, alkyl chlorides tend to be less expensive and more readily available. Alkyl chlorides readily undergo attack by nucleophiles. Heating alkyl halides with sodium hydroxide or water gives alcohols.

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