lead tetraacetate
Suppliers
Names
[ CAS No. ]:
546-67-8
[ Name ]:
lead tetraacetate
[Synonym ]:
Lead ethanoate
lead,tetraacetate
Lead(4+) tetraacetate
plumbane, tetrakis(acetyloxy)-
EINECS 208-908-0
Plumbic acetate
Lead Tetraacetate
MFCD00008693
Lead acetate, basic
Lead tetracetate
Tetraacetoxyplumbane
Chemical & Physical Properties
[ Density]:
2.22
[ Boiling Point ]:
118.1ºC
[ Melting Point ]:
175-180ºC
[ Molecular Formula ]:
C8H12O8Pb
[ Molecular Weight ]:
443.376
[ Flash Point ]:
40ºC
[ Exact Mass ]:
444.029816
[ PSA ]:
105.20000
[ Stability ]:
Stable. Moisture sensitive. Incompatible with water, most metals.
[ Water Solubility ]:
Decomposition
MSDS
Toxicological Information
CHEMICAL IDENTIFICATION
- RTECS NUMBER :
- AI5300000
- CHEMICAL NAME :
- Acetic acid, lead(4+) salt
- CAS REGISTRY NUMBER :
- 546-67-8
- LAST UPDATED :
- 199709
- DATA ITEMS CITED :
- 2
- MOLECULAR FORMULA :
- C8-H12-O8.Pb
- MOLECULAR WEIGHT :
- 443.39
Safety Information
[ Symbol ]:
GHS07, GHS08, GHS09
[ Signal Word ]:
Danger
[ Hazard Statements ]:
H302 + H332-H360Df-H373-H410
[ Precautionary Statements ]:
P201-P260-P280-P301 + P312 + P330-P308 + P313
[ Hazard Codes ]:
T:Toxic;N:Dangerousfortheenvironment;
[ Risk Phrases ]:
R20/22;R33;R50/53;R61;R62
[ Safety Phrases ]:
S45-S53-S60-S61
[ RIDADR ]:
UN 2923
[ WGK Germany ]:
3
[ RTECS ]:
AI5300000
[ Packaging Group ]:
III
[ Hazard Class ]:
6.1
[ HS Code ]:
2915299090
Precursor & DownStream
Precursor
DownStream
Customs
[ HS Code ]: 2915299090
[ Summary ]:
2915299090 salts of acetic acid。supervision conditions:AB(certificate of inspection for goods inward,certificate of inspection for goods outward)。VAT:17.0%。tax rebate rate:9.0%。MFN tariff:5.5%。general tariff:50.0%
Articles
Steroids 39(5) , 537-45, (1982)
Chem. Pharm. Bull. 50(7) , 960-3, (2002)
Lead tetraacetate oxidation of a Corynanthe-type indole alkaloid, mitragynine, produced mainly 7-acetoxyindolenine derivative (2) together with a dimeric compound (4) as a minor product. The novel str...
Steroids 58(2) , 52-8, (1993)
An efficient method for the preparation of 4 beta- and 6 alpha-hydroxylated bile acids has been developed. It involved a highly stereoselective acetoxylation at the 4 beta and 6 alpha positions of 3- ...