Iniciar sesión para ver los precios por organización y contrato.
Seleccione un Tamaño
Cambiar Vistas
Acerca de este artículo
Fórmula lineal:
[CH3(CH2)3CH(C2H5)CO2]2Sn
Número CAS:
Peso molecular:
405.12
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12161600
EC Number:
206-108-6
MDL number:
Servicio técnico
¿Necesita ayuda? Nuestro equipo de científicos experimentados está aquí para ayudarle.
Permítanos ayudarleQuality Level
assay
92.5-100.0%
reaction suitability
core: tin, reagent type: catalyst
reaction type: Ring-Opening Polymerization
refractive index
n20/D 1.493 (lit.)
density
1.251 g/mL at 25 °C (lit.)
cation traces
Na: ≤0.5%
SMILES string
CCCCC(CC)C(=O)O[SnH2]OC(=O)C(CC)CCCC
InChI
1S/2C8H16O2.Sn/c2*1-3-5-6-7(4-2)8(9)10;/h2*7H,3-6H2,1-2H3,(H,9,10);/q;;+2/p-2
InChI key
KSBAEPSJVUENNK-UHFFFAOYSA-L
Application
Tin(II) 2-ethylhexanoate is commonly used as a catalyst for the ring-opening polymerization of cyclic diesters such as L-lactide and glycolide to form high-molecular-weight polymers.
A catalyst for polylactide polymerization.
signalword
Danger
hcodes
Hazard Classifications
Aquatic Chronic 3 - Eye Dam. 1 - Repr. 1B - Skin Sens. 1
Clase de almacenamiento
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 2
flash_point_f
278.6 °F - closed cup
flash_point_c
137 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Elija entre una de las versiones más recientes:
¿Ya tiene este producto?
Encuentre la documentación para los productos que ha comprado recientemente en la Biblioteca de documentos.
Synthesis of poly (L-lactide) and polyglycolide by ring-opening polymerization.
Kaihara S
Nature Protocols, 2(11), 2767-2767 (2007)
Ali Eatemadi et al.
Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie, 84, 1915-1922 (2016-11-17)
Nano-therapy exhibit the potential of revolutionizing cancer therapy. This field introduces nanovectors/nanocarriers for anticancer drugs targeted delivery, and also finds application in imaging. Chrysin, a natural flavonoid, was recently studied as having important biological roles in chemical defenses, nitrogen fixation
Yeimy J Rodriguez et al.
Pharmaceutics, 12(3) (2020-02-29)
Amphotericin B (AmB) is a broad spectrum of antifungal drug used to treat antifungal diseases. However, due to the high toxicity of AmB, treated patients may suffer the risk of side effects, such as renal failure. Nanoencapsulation strategies have been


