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  2. S-Methylmethionine - Wikipedia

    en.wikipedia.org/wiki/S-Methylmethionine

    S-Methylmethionine (SMM) is a derivative of methionine with the chemical formula (CH 3) 2 S + CH 2 CH 2 CH(NH 3 +)CO 2 −.This cation is a naturally-occurring intermediate in many biosynthetic pathways owing to the sulfonium functional group.

  3. The best skin care routine for your 50s, according to ... - AOL

    www.aol.com/lifestyle/best-skin-care-routine-for...

    Texture: Thick, hydrating gel | Ingredients: Niacinamide, ceramides | Other benefits: Oil free, fragrance free, paraben free, sulfate free. Niacinamide — the technical name for vitamin B3 — is ...

  4. Isethionates - Wikipedia

    en.wikipedia.org/wiki/Isethionates

    Despite its low water solubility (100ppm at 25 °C), the lower-priced sodium cocoylisethionate has found more widespread use than its well water-soluble ammonium salt (> 25 wt.% at 25 °C). To solubilize the sparsely soluble isethionates and taurides, the formation of mixtures with amphoteric surfactants (such as cocamidopropyl betaine ) are ...

  5. 3-Methylpyridine - Wikipedia

    en.wikipedia.org/wiki/3-Methylpyridine

    3-Picoline is a useful precursor to agrochemicals, such as chlorpyrifos. [1] Chlorpyrifos is produced from 3,5,6-trichloro-2-pyridinol, which is generated from 3-picoline by way of cyanopyridine. This conversion involves the ammoxidation of 3-methylpyridine: CH 3 C 5 H 4 N + 1.5 O 2 + NH 3 → NCC 5 H 4 N + 3 H 2 O

  6. Alkanolamine - Wikipedia

    en.wikipedia.org/wiki/Alkanolamine

    Most proteins and peptides contain both alcohols and amino groups. Two amino acids are alkanolamines, formally speaking: serine and hydroxyproline. Veratridine and veratrine; Tropane alkaloids such as atropine; hormones and neurotransmitters epinephrine (adrenaline) and norepinephrine (noradrenaline)

  7. Glycolic acid - Wikipedia

    en.wikipedia.org/wiki/Glycolic_acid

    It is used as a monomer in the preparation of polyglycolic acid and other biocompatible copolymers (e.g. PLGA). Commercially, important derivatives include the methyl (CAS# 96-35-5) and ethyl (CAS# 623-50-7) esters which are readily distillable (boiling points 147–149 °C and 158–159 °C, respectively), unlike the parent acid.

  8. Aminomethyl group - Wikipedia

    en.wikipedia.org/wiki/Aminomethyl_group

    Usually aminomethyl groups feature tertiary amines. Often they are obtained by alkylation with Eschenmoser's salt, a source of [CH 2 =N(CH 3) 2] +. A cobalt(III) complex of aminomethyl is known in the form [Co 2 (CH 2 NH 2)](ClO4) 2. [1] Aminomethyl is the first member of a series of 1-aminoalkyl groups of the form −(CH 2 −) n NH 2. [2]

  9. Pentenoic acid - Wikipedia

    en.wikipedia.org/wiki/Pentenoic_acid

    2-Amino-5-chloro-4-pentenoic acid, found in the mushroom Amanita cokeri; 2-Methyl-3-pentenoic acid. Some esters are berry fruit flavors. [18] 2-Propyl-trans-2-pentenoic acid (2-en-valproic acid), major metabolite of anticonvulsant valproic acid. [19] cis-2-methyl-2-pentenoic acid 2-methyl-(2Z)-pent-2-enoic acid. (CAS 1617-37-4, FDA 07B8HQZ433 ...