265640
Tin
powder, <150 μm, 99.5% trace metals basis
Synonyme(s) :
Sn
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About This Item
Formule empirique (notation de Hill):
Sn
Numéro CAS:
Poids moléculaire :
118.71
Numéro CE :
Numéro MDL:
Code UNSPSC :
12161600
ID de substance PubChem :
Nomenclature NACRES :
NA.22
Produits recommandés
Niveau de qualité
Pureté
99.5% trace metals basis
Forme
powder
Pertinence de la réaction
core: tin
reagent type: catalyst
Résistivité
11 μΩ-cm, 20°C
Taille des particules
<150 μm
Point d'ébullition
2270 °C (lit.)
Pf
231.9 °C (lit.)
Densité
7.310 g/mL at 25 °C (lit.)
Chaîne SMILES
[Sn]
InChI
1S/Sn
Clé InChI
ATJFFYVFTNAWJD-UHFFFAOYSA-N
Catégories apparentées
Description générale
Tin is an efficient catalyst for the polycondensation of lactic acid to synthesize poly(lactic acid).
Application
With HCl, reduces a variety of functional groups; stereoselective allylation of carbonyl compounds; in situ generation of tin enolates for directed aldol reactions.
Code de la classe de stockage
13 - Non Combustible Solids
Classe de danger pour l'eau (WGK)
WGK 3
Point d'éclair (°F)
Not applicable
Point d'éclair (°C)
Not applicable
Équipement de protection individuelle
dust mask type N95 (US), Eyeshields, Gloves
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A series of rutile-type (Ti,Sn)O2 solid solutions with nanorod architecture were successfully synthesized in this study by varying their calcination temperatures of tin-modified titanium dioxide (Sn/TiO2) nanocomposites under a nitrogen atmosphere. During the delithiation process, the (Ti,Sn)O2 nanorods obtained at
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The kesterite-structured semiconductors Cu2ZnSnS4 and Cu2ZnSnSe4 are drawing considerable attention recently as the active layers in earth-abundant low-cost thin-film solar cells. The additional number of elements in these quaternary compounds, relative to binary and ternary semiconductors, results in increased flexibility
D B Shpakovsky et al.
Dalton transactions (Cambridge, England : 2003), 41(48), 14568-14582 (2012-10-12)
Four new organotin(IV) complexes of bis-(2,6-di-tert-butylphenol)tin(IV) dichloride [(tert-Bu-)(2)(HO-Ph)](2)SnCl(2) (1) with the heterocyclic thioamides 2-mercapto-pyrimidine (PMTH), 2-mercapto-4-methyl-pyrimidine (MPMTH), 2-mercapto-pyridine (PYTH) and 2-mercapto-benzothiazole (MBZTH), of formulae {[(tert-Bu-)(2)(HO-Ph)](2)Sn(PMT)(2)} (2), {[(tert-Bu-)(2)(HO-Ph)](2)Sn(MPMT)(2)} (3), {[(tert-Bu-)(2)(HO-Ph)](2)SnCl(PYT)} (4) and {[(tert-Bu-)(2)(HO-Ph)](2)SnCl(MBZT)} (5), have been synthesized and characterized by elemental
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