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Lead(IV) acetate, 96% (dry wt.), stab. with 5-10% glacial acetic acid

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Regulatorisk: Dette produkt falder ind under Lov om kemiske stoffer og produkter - lovbekendtgørelse nr. 1755 af 22. december 2006. Hvis det er relevant, skal kunden fremskaffe en licens før levering.
Artikelnummer. 11482987 Leverandør Thermo Scientific Alfa Aesar Leverandørnr. A15551.18
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CAS: 546-67-8 | C8H12O8Pb | 443.40 g/mol

Lead(IV) acetate is an important oxidizing agent and a source of acetyloxy group used in organic synthesis. For example, 1,4-dioxene is prepared from dioxane involving 2-acetoxy-1,4-dioxane as an intermediate. Similarly, it is used for the preparation of bis(trifluoromethyl)diazomethane from hexafluoroacetone hydrazone. It also reacts with alkenes, alcohols having a delta-proton and di-n-butyl d-tartrate to get gamma-lactones, cyclic ethers and n-butyl glyoxylate respectively. It induces the cleavage of 1,2-diols to the corresponding aldehydes or ketones. It is actively involved in the Kochi reaction for the decarboxylation of carboxylic acids to alkyl halides and used as an alternative reagent to bromine in the Hofmann rearrangement.

This Thermo Scientific brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific.

Applications
Lead(IV) acetate is an important oxidizing agent and a source of acetyloxy group used in organic synthesis. For example, 1,4-dioxene is prepared from dioxane involving 2-acetoxy-1,4-dioxane as an intermediate. Similarly, it is used for the preparation of bis(trifluoromethyl)diazomethane from hexafluoroacetone hydrazone. It also reacts with alkenes, alcohols having a delta-proton and di-n-butyl d-tartrate to get gamma-lactones, cyclic ethers and n-butyl glyoxylate respectively. It induces the cleavage of 1,2-diols to the corresponding aldehydes or ketones. It is actively involved in the Kochi reaction for the decarboxylation of carboxylic acids to alkyl halides and used as an alternative reagent to bromine in the Hofmann rearrangement.

Solubility
Soluble in water, ethanol, chloroform, benzene, nitrobenzene, tetrachloroethane, nitric acid, hot acetic acid and hydrochloric acid.

Notes
Air and moisture sensitive. Store in cool place. Keep the container tightly closed in a dry and well-ventilated place. Incompatible with alcohols, strong acids and strong reducing agents.
TRUSTED_SUSTAINABILITY

Spezifikation

Kemisk navn eller materiale Lead(IV) acetate
Navn note stabilized with 5 to 10% glacial acetic acid
CAS 546-67-8
Smeltepunkt 175°C
Tæthed 2.28
Assay Procent Noter (dry wt.)
Molekylær formel C8H12O8Pb
Lineær formel Pb(OOCCH3)4
MDL nummer MFCD00008693
Mængde 50 g
FN nummer UN1616
Beilstein 3595640
Følsomhed Moisture sensitive
Merck Index 14,5423
Synonym lead iv acetate
Opløselighedsinformation Soluble aq. soln.,ethanol,chloroform,benzene,nitrobenzene,tetrachloroethane,nitric acid,hot acetic acid and hydrochloric acid.
InChI nøgle ACKFDYCQCBEDNU-UHFFFAOYSA-J
SMIL [Pb++].CC([O-])=O.CC([O-])=O.CC([O-])=O.CC([O-])=O
IUPAC navn λ²-lead(2+) tetraacetate
Molekylvægt (g/mol) 443.40
PubChem CID 50931538
Formel vægt 443.37
Procent renhed 96%
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Produktidentifikator
  • Lead(IV) acetate, stabilized with 5-10% glacial acetic acid
Signalwort
  • Fare
Gefahrenkategorie
  • Akut toksicitet Kategori 4
  • LANGTIDSFARE FOR VANDMILJØET Kronisk kategori 1
  • AKUT FARE FOR VANDMILJØET Akut kategori 1
  • Reproduktionstoksicitet Kategori 1A
  • Specifik målorgantoksicitet efter gentagen eksponering Kategori 2
Gefahrenhinweis
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Sicherheitshinweis
  • P264-Vask grundigt efter brug.
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  • P312-I tilfælde af ubehag, ring til en GIFTINFORMATION/læge/ .
Ergänzende Informationen
  • MIXTURE LIST-Contain: Acetic acid, lead(4+) salt

RUO – Research Use Only

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