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S3252

Sigma-Aldrich

Tin(II) 2-ethylhexanoate

92.5-100.0%

Synonym(s):

2-Ethylhexanoic acid tin(II) salt, Stannous 2-ethylhexanoate, Stannous octoate

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About This Item

Linear Formula:
[CH3(CH2)3CH(C2H5)CO2]2Sn
CAS Number:
301-10-0
Molecular Weight:
405.12
EC Number:
206-108-6
MDL number:
MFCD00002676
UNSPSC Code:
12161600
PubChem Substance ID:
57654612
NACRES:
NA.22

Quality Level

200

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

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Application

A catalyst for polylactide polymerization.
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.

Signal Word

Danger

Hazard Statements

H317,H318,H360D,H412

Hazard Classifications

Aquatic Chronic 3 - Eye Dam. 1 - Repr. 1B - Skin Sens. 1

Storage Class Code

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

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
0000389537
0000376190
0000343120
0000376190
0000326921

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Synthesis of poly (L-lactide) and polyglycolide by ring-opening polymerization.
Kaihara S
Nature Protocols, 2(11), 2767-2767 (2007)
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With the aim to develop biomaterials for temporary medical devices, a series of novel reducible and/or degradable elastomers has been prepared from PLA-b-PEG-b-PLA copolymers photo-crosslinked with diallyl sulfide or pentaerythritol tetrakis(3-mercaptopropionate). Thermal and mechanical properties, including elastic limit and Young
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
Meng-Huang Wu et al.
PloS one, 12(10), e0186784-e0186784 (2017-10-24)
This study evaluates the sustained analgesic effect of ketorolac-eluting thermosensitive biodegradable hydrogel in the plantar incisional pain model of the rat hind-paw. A ketorolac-embedded 2, 2'-Bis (2-oxazolin) (BOX) linking methoxy-poly(ethylene glycol) and poly(lactide-co-glycolide) (mPEG-PLGA) diblock copolymer (BOX copolymer) was synthesized
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