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Caprylylglycine

  • Name: Caprylylglycine
  • CAS: 14246-53-8
  • Purity: 99%
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  • Description

    Reliable factory customized supply Caprylylglycine 14246-53-8

    • Molecular Formula: C10H19NO3
    • Molecular Weight: 201.266
    • Appearance/Colour: White crystalline powder 
    • Vapor Pressure: 0.000448mmHg at 25°C 
    • Melting Point: 102-103 °C 
    • Refractive Index: 1.455 
    • Boiling Point: 403.868 °C at 760 mmHg 
    • PKA: 3.62±0.10(Predicted) 
    • Flash Point: 198.052 °C 
    • PSA： 66.40000 
    • Density: 1.037 g/cm3 
    • LogP: 1.93860 

    Caprylylglycine(Cas 14246-53-8) Usage

    Definition

    ChEBI: An N-acylglycine with an acyl group that is octanoyl.

    InChI:InChI=1/C10H21NO2/c1-2-3-4-5-6-7-8-11-9-10(12)13/h11H,2-9H2,1H3,(H,12,13)

    14246-53-8 Relevant articles

    NMR-based assignment of isoleucine: Vs. allo -isoleucine stereochemistry

    Anderson, Zoe J.,Hobson, Christian,Needley, Rebecca,Song, Lijiang,Perryman, Michael S.,Kerby, Paul,Fox, David J.

    , p. 9372 - 9378 (2017)

    A simple 1H and 13C NMR spectrometric an...

    Repurposing the 3-Isocyanobutanoic Acid Adenylation Enzyme SfaB for Versatile Amidation and Thioesterification

    Zhu, Mengyi,Wang, Lijuan,He, Jing

    supporting information, p. 2030 - 2035 (2020/11/30)

    Genome mining of microbial natural produ...

    A modular approach towards drug delivery vehicles using oxanorbornane-based non-ionic amphiphiles

    Janni, D. Sirisha,Reddy, U. Chandrasekhar,Saroj, Soumya,Muraleedharan

    supporting information, p. 8025 - 8032 (2016/12/18)

    The self-assembly of non-ionic amphiphil...

    Antimicrobial Preservative Compositions for Personal Care Products

    -

    Paragraph 0061, (2014/10/29)

    A personal product antimicrobial preserv...

    14246-53-8 Process route

    glycine
    56-40-6,18875-39-3,25718-94-9

    glycine

    n-octanoic acid chloride
    111-64-8

    n-octanoic acid chloride

    N-(1-oxooctyl)glycine
    14246-53-8

    N-(1-oxooctyl)glycine

    Conditions
    Conditions Yield
    With potassium carbonate; potassium hydroxide; In tetrahydrofuran; water; at 20 - 22 ℃; for 72h;
    		86%
    With sodium hydroxide; In water; acetone;
    		83%
    With sodium hydroxide; In water; acetone; at 0 - 5 ℃;
    		72%
    With triethylamine; In water; acetone; at 0 - 20 ℃;
    		65%
    sodium hydroxide; In water;
    		28%
    sodium hydroxide; In water;
    		28%
    With sodium hydroxide; for 1h; Ambient temperature;
    		18.5 g
    With sodium hydroxide; In water; at 15 - 20 ℃; for 1h; pH=10 - 10.5; Inert atmosphere;
    With sodium hydroxide; In water; acetone; at 0 - 20 ℃; pH=8.5 - 10.5;
    With sodium hydroxide; In water; at 20 ℃; for 1h; pH=10 - 10.5; Inert atmosphere;
    With sodium hydroxide; In water; at 15 - 20 ℃; for 1h; pH=10 - 10.5; Inert atmosphere;
    C11 H21 NO3

    C11 H21 NO3

    N-(1-oxooctyl)glycine
    14246-53-8

    N-(1-oxooctyl)glycine

    Conditions
    Conditions Yield
    With water; lithium hydroxide; In tetrahydrofuran; at 20 ℃; for 12h;
    		100%
    C11H21NO3; With lithium hydroxide; In methanol; water; at 20 ℃; for 2h;
    With hydrogenchloride; In methanol; water; pH=3;

    14246-53-8 Upstream products

    • 56-40-6
      56-40-6

      glycine

    • 111-64-8
      111-64-8

      n-octanoic acid chloride

    • 544-31-0
      544-31-0

      2-(palmitoylamino)ethanol

    • 111-57-9
      111-57-9

      N-stearoylethanolamine

    14246-53-8 Downstream products

    • 335097-74-0
      335097-74-0

      C18 H28 N2 O2

    • 1190867-32-3
      1190867-32-3

      C19 H30 N2 O2

    • 1190851-42-3
      1190851-42-3

      C18 H34 N2 O2

    • 1190851-39-8
      1190851-39-8

      C20 H32 N2 O2

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