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线性分子式:
C11H16N5O · BF4
化学文摘社编号:
分子量:
321.08
NACRES:
NA.21
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Beilstein/REAXYS Number:
7066325
产品名称
O -(苯并三唑-1-基)- N,N,N′,N′-四甲基脲四氟硼酸盐, ≥97.0% (N)
InChI
1S/C11H16N5O.BF4/c1-14(2)11(15(3)4)17-16-10-8-6-5-7-9(10)12-13-16;2-1(3,4)5/h5-8H,1-4H3;/q+1;-1
SMILES string
F[B-](F)(F)F.CN(C)\C(On1nnc2ccccc12)=[N+](/C)C
InChI key
JKEKMBGUVUKMQB-UHFFFAOYSA-N
assay
≥97.0% (N)
form
solid
mp
205 °C (dec.) (lit.)
solubility
acetonitrile: 0.1 g/mL, clear, colorless
application(s)
peptide synthesis
storage temp.
2-8°C
Quality Level
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Application
非常适用于固相肽合成的偶联剂。
Other Notes
最近的研究显示,该偶联剂的晶体结构和溶液结构都是 N-氧化胍,而不是铀化合物 ;偶联试剂,最适用于固相多肽合成。
signalword
Danger
hcodes
Hazard Classifications
Flam. Sol. 1 - Skin Sens. 1A
存储类别
4.1A - Other explosive hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Samer Al-Gharabli et al.
Materials (Basel, Switzerland), 11(5) (2018-05-08)
Advanced ceramic materials with a well-defined nano-architecture of their surfaces were formed by applying a two-step procedure. Firstly, a primary amine was docked on the ordered nanotubular ceramic surface via a silanization process. Subsequently, single-wall carbon nanotubes (SWCNTs) were covalently
S. Zimmer et al. et al.
Proc. 22nd Eur. Pept. Symp.: Peptides 1992 null
Rajni Bala et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 196, 268-273 (2018-02-20)
In the present study, we report a highly sensitive, rapid and low cost colorimetric monitoring of malathion (an organophosphate insecticide) employing a basic hexapeptide, malathion specific aptamer (oligonucleotide) and silver nanoparticles (AgNPs) as a nanoprobe. AgNPs are made to interact
O-(BENZOTRIAZOL-1-YL)-N, N, N', N'-TETRAMETHYLURONIUM TETRAFLUOROBORATE (TBTU): A NEW REAGENT FOR THE CLEAVAGE OF TETRAHYDROPYRANYL, SILYL AND 4, 4'-D IMETHOXYTRITYL ETHERS.
Ramasamy KS and Averett D.
Synlett, 6, 709-712 (1999)
Parvin Zakeri-Milani et al.
EXCLI journal, 16, 650-662 (2017-07-12)
Gemcitabine (Gem) is used as a single agent or in combination with other anticancer agents to treat many types of solid tumors. However, it has many limitations such as a short plasma half-life, dose-limiting toxicities and drug resistance. Cell-penetrating peptides
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