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15370

Sigma-Aldrich

Lead tetraacetate

purum p.a., moistened with ~5% acetic acid to stabilize, ≥95% (dried material)

Synonym(s):

Lead(IV) acetate

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About This Item

Linear Formula:
Pb(CH3COO)4
CAS Number:
546-67-8
Molecular Weight:
443.38
Beilstein/REAXYS Number:
3595640
MDL number:
MFCD00008693
UNSPSC Code:
12352202
PubChem Substance ID:
329750835
assay:
≥95% (dried material)
form:
solid

grade

purum p.a.

assay

≥95% (dried material)

form

solid

quality

moistened with ~5% acetic acid to stabilize

SMILES string

CC(=O)O[Pb](OC(C)=O)(OC(C)=O)OC(C)=O

InChI

1S/4C2H4O2.Pb/c4*1-2(3)4;/h4*1H3,(H,3,4);/q;;;;+4/p-4

InChI key

JEHCHYAKAXDFKV-UHFFFAOYSA-J

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Application

For the preparation of a dip reagent for the fluorimetric determination of diols, glycosides and phenols (see also 35848 2′,7′-Dichlorofluorescein)

signalword

Danger

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Repr. 1A - STOT RE 2

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

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Journal of the American Chemical Society, 131(33), 11998-12006 (2009-08-06)
A series of seven cyclopent-3-en-1-ylmethylamines bearing one, two, or three methyl substituents at the C2, C3, C4, or C(alpha) positions, including the unsubstituted parent, was accessed by ring-closing metatheses of alpha,alpha-diallylacetonitrile (or methallyl variants) and alpha,alpha-diallylacetone followed by hydride reductions
Glycol-cleavage oxidation.
Arthur S Perlin
Advances in carbohydrate chemistry and biochemistry, 60, 183-250 (2006-06-06)
T H Ma et al.
Mutation research, 270(1), 71-77 (1992-11-01)
Synergistic and antagonistic effects on genotoxicity of mixtures of four chemicals; i.e., lead tetraacetate (LTA), arsenic trioxide (ATO), dieldrin (DED), and tetrachloroethylene (TCE), were evaluated by the Tradescantia-micronucleus (Trad-MCN) assay. The chemicals were mixed in ratios of 1:1, 1:2 and
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Two naturally occurring 11-nordrimanes were synthesized, and their (1)H and (13)C NMR spectra were unambiguously assigned in full for the first time.
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