T84964
三炔丙基胺
98%
别名:
三（2-丙炔基）胺
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关于此项目
线性分子式:
(HC≡CCH2)3N
化学文摘社编号:
分子量:
131.17
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
230-038-5
MDL number:
Assay:
98%
InChI
1S/C9H9N/c1-4-7-10(8-5-2)9-6-3/h1-3H,7-9H2
InChI key
ZHOBJWVNWMQMLF-UHFFFAOYSA-N
SMILES string
C#CCN(CC#C)CC#C
assay
98%
refractive index
n20/D 1.484 (lit.)
bp
79-85 °C/11 mmHg (lit.)
density
0.927 g/mL at 25 °C (lit.)
storage temp.
2-8°C
Quality Level
Application
铜三丙基丙胺被广泛用于铜催化的烷基叠氮环加成 (CuAAC) click 反应合成三（3-羟丙基三唑甲基）胺 (THPTA) 和三 [（1-苄基-1H-1,2,3-三唑-4-基）甲基] 胺 (TBTA) 等 Cu (i) 稳定配体。
它也可用于蒽系三足类化合物三 [（9-蒽基苄基-1 H -1,2,3-三唑-4-基）甲基] 胺的合成，作为水溶液中 Ni 2 + 荧光识别的受体。
它也可用于蒽系三足类化合物三 [（9-蒽基苄基-1 H -1,2,3-三唑-4-基）甲基] 胺的合成，作为水溶液中 Ni 2 + 荧光识别的受体。
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
3 - Flammable liquids
wgk
WGK 3
flash_point_f
134.6 °F - closed cup
flash_point_c
57 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
危险化学品
此项目有
Polytriazoles as copper (I)-stabilizing ligands in catalysis.
Chan T R, et al.
Organic Letters, 6(17), 2853-2855 (2004)
Qian Zhang et al.
ChemistryOpen, 8(5), 571-579 (2019-05-09)
An azide terminated ethylene oxide-tetrahydrofuran copolymer with urethane segments (ATUPET) as a novel binder pre-polymer, has been prepared through ethylene oxide-tetrahydrofuran random copolymer (PET) end-capping modification via one-pot method. The structure characterization of the modifier has been analyzed by FTIR
Analysis and Optimization of Copper?Catalyzed Azide?Alkyne Cycloaddition for Bioconjugation.
Hong V, et al.
Angewandte Chemie (International Edition in English), 48(52), 9879-9883 (2009)
Click grafting of alkyne-containing vinyl polymers onto biosynthesized extracellular matrix protein containing azide functionality and adhesion control of human umbilical vein endothelial cells.
Yamada T and Takasu A
Royal Society of Chemistry Advances, 5(52), 41445-41456 (2015)
Cu (II)-Catalyzed Oxidative Formation of 5, 5′-Bistriazoles.
Brassard C J, et al.
The Journal of Organic Chemistry, 81(24), 12091-12105 (2016)
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