[A15551] CAS 546-67-8 | Lead(IV) acetate, 96% (dry wt.), stab. with 5-10% glacial acetic acid | Alfa

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Brand: Alfa Aesar

546-67-8 | C8H12O8Pb | lead(IV) acetate

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Chemical Identifiers

CAS
546-67-8
Molecular Weight (g/mol)
443.40
Synonym
lead(IV) acetate
SMILES
[Pb++].CC([O-])=O.CC([O-])=O.CC([O-])=O.CC([O-])=O
InChI Key
ACKFDYCQCBEDNU-UHFFFAOYSA-J
Molecular Formula
C8H12O8Pb
IUPAC Name
λ²-lead(2+) tetraacetate

Specifications

Comment
May contain fine dark particles from the manufacturing process
Form
Moist crystals or powder or crystalline powder
Appearance (Color)
White to pale cream or pale grey
Assay from Supplier’s CofA
≥95.0% (ex Pb; dry wt. basis, Iodometry)

설명

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 Chemicals 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 Chemicals.

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.

Other References:

Merck Index:14,5423UN Number:UN1616Beilstein:3595640

GHS Hazard and Precautionary Statements

Hazard Statements:H302+H332-H314-H335-H350-H360Df-H373
GHS H StatementH360-H373-H302-H332-H201May damage fertility or the unborn child.May cause damage to organs through prolonged or repeated exposure.Harmful if swallowed.Harmful if inhaled.Explosive; mass explosion hazard.
Precautionary Statements:P201-P202-P260-P264b-P270-P271-P281-P303+P361+P353-P304+P340-P305+P351+P338-P310-P330-P331-P363-P501c

Risk & Safety

TSCA:YesRTECS Number:AI5300000

경고:RUO – Research Use Only

CAS546-67-8FORMULAC8H12O8PbHAZARD CLASS6.1EINECS208-908-0MDLMFCD00008693PACKAGING GROUPIII

Pakage

1000g, 100g, 250g, 50G

brand

Alfa Aesar

SKU: A15551 Category:  Brand:
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[A15551] CAS 546-67-8 | Lead(IV) acetate, 96% (dry wt.), stab. with 5-10% glacial acetic acid | Alfa

[A15551] CAS 546-67-8 | Lead(IV) acetate, 96% (dry wt.), stab. with 5-10% glacial acetic acid | Alfa

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