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344931

Sigma-Aldrich

Butyltin hydroxide oxide hydrate

97%

Synonym(s):

Butylhydroxyoxostannane

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About This Item

Linear Formula:
CH3(CH2)3Sn(=O)OH·xH2O
CAS Number:
336879-56-2
Molecular Weight:
208.83 (anhydrous basis)
MDL number:
MFCD03424122
UNSPSC Code:
12352103
PubChem Substance ID:
24861279
NACRES:
NA.22

Assay

97%

SMILES string

O.CCCC[Sn](O)=O

InChI

1S/C4H9.2H2O.O.Sn/c1-3-4-2;;;;/h1,3-4H2,2H3;2*1H2;;/q;;;;+1/p-1

InChI key

KBNBFLVBJDYEFE-UHFFFAOYSA-M

Application

Butyltin hydroxide oxide hydrate can be used:
  • As a starting material for the preparation of 1,3,2-oxathiastannolane derivatives.
  • To prepare polyethylene oxide (PEO) ionomer i.e, PEO600/sulphoisophthalate Na ionomer.
  • To prepare sulfonated copolyester (SPE) polymers.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Silica nanoparticles densely grafted with PEO for ionomer plasticization
O'Reilly MV and Winey KI
Royal Society of Chemistry Advances, 5(25), 19570-19580 (2015)
Dimeric dithiocarbamates of stannolane. An example of the presence of secondary bonds in the formation of an inorganic ring. Molecular and crystal structure of 2-nbutyl-2-(dimethyldithiocarbamate)-1, 3, 2-oxathiastannolane and 2-nbutyl-2-(piperidyldithioca
Gomez-Ortiz LA, et al.
Journal of Organometallic Chemistry, 654(1-2), 51-55 (2002)
A facile preparation of microparticles from sulfonated polyester nanoparticles via emulsion-aggregation process
Subramani S, et al.
Colloids and Surfaces. A, Physicochemical and Engineering Aspects, 340(1-3), 40-49 (2009)
David W Sanders et al.
eLife, 10 (2021-04-24)
Many enveloped viruses induce multinucleated cells (syncytia), reflective of membrane fusion events caused by the same machinery that underlies viral entry. These syncytia are thought to facilitate replication and evasion of the host immune response. Here, we report that co-culture

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