Home Cart Sign in  
Chemical Structure| 52315-75-0 Chemical Structure| 52315-75-0

Structure of H-Lys(Lauroyl)-OH
CAS No.: 52315-75-0

Chemical Structure| 52315-75-0

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

,{[proInfo.pro_purity]}

4.5 *For Research Use Only !

{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]} Purity: {[proInfo.pro_purity]}

Change View

Size Price VIP Price

US Stock

Global Stock

In Stock
{[ item.pr_size ]} Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}

US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days

  • {[ item.pr_size ]}

In Stock

- +

Please Login or Create an Account to: See VIP prices and availability

US Stock: ship in 0-1 business day
Global Stock: ship in 2 weeks

  • 1-2 Day Shipping
  • High Quality
  • Technical Support
Product Citations

Alternative Products

Product Details of [ 52315-75-0 ]

CAS No. :52315-75-0
Formula : C18H36N2O3
M.W : 328.49
SMILES Code : N[C@@H](CCCCNC(CCCCCCCCCCC)=O)C(O)=O
MDL No. :MFCD09954506
InChI Key :GYDYJUYZBRGMCC-INIZCTEOSA-N
Pubchem ID :104151

Safety of [ 52315-75-0 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 52315-75-0 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Upstream synthesis route of [ 52315-75-0 ]
  • Downstream synthetic route of [ 52315-75-0 ]

[ 52315-75-0 ] Synthesis Path-Upstream   1~2

  • 1
  • [ 111-82-0 ]
  • [ 59409-41-5 ]
  • [ 52315-75-0 ]
YieldReaction ConditionsOperation in experiment
32% at 80℃; for 54 h; Inert atmosphere General procedure: Commercially available ionized liquid tetrabutylphosphonium glycinate (Gly-TBP, manufactured by Katayama Pharmaceutical Co., Ltd., colorless transparent liquid, moisture content: 0.11 mass percent) was used as the component (A).In a high purity argon atmosphere, Lau-OMe was added to 1 kg of the above Gly-TBP so that the amount of methyl laurate (Lau-OMe, Wako Pure Chemical Industries, Ltd.) was 500 mmol (Gly-TBP: Lau-OMe molar ratio = 6: 1). After thorough stirring of the obtained solution, it was confirmed that the whole solution became homogeneous, and then the reaction was started by heating to 60 ° C. while stirring in a water bath. Each time-lapse sample was analyzed by HPLC to confirm formation of N-acylamino acid (N-lauroylglycine). After 86 hours, the yield of N-acylamino acid (N-lauroylglycine) was about 82percent
References: [1] Patent: JP6011999, 2016, B2, . Location in patent: Paragraph 0024; 0026; 0027; 0029.
  • 2
  • [ 143-07-7 ]
  • [ 56-87-1 ]
  • [ 59409-41-5 ]
  • [ 52315-75-0 ]
References: [1] Journal of Agricultural and Food Chemistry, 2006, vol. 54, # 1, p. 72 - 78.
 

Historical Records