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Warning
危险分类
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
储存分类代码
10 - Combustible liquids
WGK
WGK 3
闪点(°F)
235.4 °F - closed cup
闪点(°C)
113 °C - closed cup
个人防护装备
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, 6(8), 781-789 (1991-08-01)
We have chemically synthesized the full-length, 84 amino acid, human parathyroid hormone (hPTH) on a greater than 100 mg scale by the Merrifield solid-phase technique of stepwise peptide synthesis using a benzhydrylamine support. The peptide was purified by high-performance liquid
Benzhydrylamine linker grafting: a strategy for the improved synthesis of C-terminal peptide amides.
Journal of peptide science : an official publication of the European Peptide Society, 16(10), 551-557 (2010-09-24)
The standard p-MBHA resin used during Boc-chemistry synthesis of peptides carrying C-terminal carboxamides is compromised by batch-to-batch variations in its performance. This can cause artificially 'difficult' couplings during peptide chain assembly, which may ultimately lead to failed syntheses given the
Chemistry (Weinheim an der Bergstrasse, Germany), 18(18), 5693-5700 (2012-03-23)
A robust heterogeneous self-supported chiral titanium cluster (SCTC) catalyst and its application in the enantioselective imine-cyanation/Strecker reaction is described under batch and continuous processes. One of the major hurdles in the asymmetric Strecker reaction is the lack of availability of
Journal of peptide science : an official publication of the European Peptide Society, 16(10), 545-550 (2010-09-09)
Well-characterized resins of high purity are critical for effective solid phase peptide synthesis (SPPS). The quality of commercial (4-methyl)benzhydrylamine-resin (MBHA-resin), used for the synthesis of peptide amides, is not consistent and residual ketone functionalities are frequently present. Such ketone or
Adrenergic blocking drugs; blocking of excitatory responses to epinephrine and adrenergic nerve stimulation with N-alkyl-N-(2-chloroethyl)-benzhydrylamines.
The Journal of pharmacology and experimental therapeutics, 97(4), 441-449 (1949-12-01)
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