T84964
Tripropargylamine
98%
Sinonimo/i:
Tris(2-propynyl)amine
Autenticatiper visualizzare i prezzi riservati alla tua organizzazione & contrattuali
About This Item
Formula condensata:
(HC≡CCH2)3N
Numero CAS:
Peso molecolare:
131.17
Numero CE:
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22
Prodotti consigliati
![Tris[(1-benzyl-1H-1, 2, 3-triazol-4-yl)methyl]amine 97%](/deepweb/assets/sigmaaldrich/product/structures/179/695/86a721c8-2a4c-4e4f-bc36-6276ce7a941f/640/86a721c8-2a4c-4e4f-bc36-6276ce7a941f.png)
Saggio
98%
Indice di rifrazione
n20/D 1.484 (lit.)
P. eboll.
79-85 °C/11 mmHg (lit.)
Densità
0.927 g/mL at 25 °C (lit.)
Temperatura di conservazione
2-8°C
Stringa SMILE
C#CCN(CC#C)CC#C
InChI
1S/C9H9N/c1-4-7-10(8-5-2)9-6-3/h1-3H,7-9H2
ZHOBJWVNWMQMLF-UHFFFAOYSA-N
Categorie correlate
Applicazioni
Tripropargylamine is widely used in the synthesis of Cu(I) stabilizing ligands such as tris(3-hydroxypropyltriazolylmethyl)amine (THPTA) and tris[(1-benzyl-1H-1,2,3-triazol-4-yl)methyl]amine (TBTA) for the copper-catalyzed alkyne-azide cycloaddition (CuAAC) click reaction.
It can also be used in the synthesis of anthracene appended tripodal triazole, tris[(9-anthryl benzyl-1H-1,2,3-triazole-4-yl)methyl]amine as a receptor for fluorescence recognition of Ni2+ in aqueous solution.
It can also be used in the synthesis of anthracene appended tripodal triazole, tris[(9-anthryl benzyl-1H-1,2,3-triazole-4-yl)methyl]amine as a receptor for fluorescence recognition of Ni2+ in aqueous solution.
Avvertenze
Warning
Indicazioni di pericolo
Consigli di prudenza
Classi di pericolo
Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
Organi bersaglio
Respiratory system
Codice della classe di stoccaggio
3 - Flammable liquids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
134.6 °F - closed cup
Punto d’infiammabilità (°C)
57 °C - closed cup
Dispositivi di protezione individuale
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Scegli una delle versioni più recenti:
Possiedi già questo prodotto?
I documenti relativi ai prodotti acquistati recentemente sono disponibili nell’Archivio dei documenti.
I clienti hanno visto anche
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)
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)
A new click-derived tripodal receptor for fluorescence recognition of Ni2+ in aqueous solution.
Zhu J H, et al.
Inorgorganica Chimica Acta, 451, 111-115 (2016)
Cu (II)-Catalyzed Oxidative Formation of 5, 5′-Bistriazoles.
Brassard C J, et al.
The Journal of Organic Chemistry, 81(24), 12091-12105 (2016)
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
Il team dei nostri ricercatori vanta grande esperienza in tutte le aree della ricerca quali Life Science, scienza dei materiali, sintesi chimica, cromatografia, discipline analitiche, ecc..
Contatta l'Assistenza Tecnica.