Benzylamine hydrochloride
Reference standards.
Inquire / Order:
manager@chemfaces.com
Technical Inquiries:
service@chemfaces.com
Tel:
+86-27-84237783
Fax:
+86-27-84254680
Address:
1 Building, No. 83, CheCheng Rd., Wuhan Economic and Technological Development Zone, Wuhan, Hubei 430056, PRC
Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to
24 months(2-8C).
Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.
Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com
The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.
Academic J of Second Military Medical University2018, 39(11)
LWT - Food Science and Technology2022, 164:113627
Ann Transl Med.2019, 7(23):731
Natural Product Communications2020, doi: 10.1177.
Mol Cells.2015, 38(9):765-72
Antioxidants (Basel).2024, 13(12):1530.
Journal of Third Military Medical University2019, 41(2):110-115
Eur Rev Med Pharmacol Sci.2020, 24(9):5127-5139.
BMC Plant Biol.2020, 20(1):214.
ACS Synth Biol.2022, 11(10):3296-3304.
Related and Featured Products
The Journal of Organic Chemistry, 1997, 62(4):903-907.
Synthesis of Azasugars via Lanthanide-Promoted Aza Diels−Alder Reactions in Aqueous Solution.[Reference:
WebLink]
METHODS AND RESULTS:
Aqueous aza Diels−Alder reactions of chiral aldehydes, prepared from carbohydrates, with Benzylamine hydrochloride and cyclopentadiene, were promoted by lanthanide triflates. The exo/endo selectivities and diastereoselectivities of the reactions were elucidated by NMR, CD spectroscopy, and X-ray crystallography. The nitrogen-containing heterocyclic products were further transformed to azasugars, which are potential inhibitors against glycoprocessing enzymes.
