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Details

Stereochemistry ACHIRAL
Molecular Formula 2C2H3O2.Pb
Molecular Weight 325.3
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LEAD ACETATE ANHYDROUS

SMILES

[PbH2++].CC([O-])=O.CC([O-])=O

InChI

InChIKey=NJJJCKUBWUKYFT-UHFFFAOYSA-L
InChI=1S/2C2H4O2.Pb.2H/c2*1-2(3)4;;;/h2*1H3,(H,3,4);;;/q;;+2;;/p-2

HIDE SMILES / InChI

Molecular Formula Pb
Molecular Weight 207.2
Charge 2
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C2H3O2
Molecular Weight 59.044
Charge -1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Lead(II) acetate is a white crystalline chemical compound with a sweetish taste. Lead(II) acetate is used as a mordant in textile printing and dyeing, as a drier in paints and varnishes, and in preparing other lead compounds. It was historically used as a sweetener and for cosmetics.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
PubMed

PubMed

TitleDatePubMed
The mechanism of the lead tetraacetate oxidation of a B-norsteroid.
1967 Aug 15
Chromosomal effects of lead: A critical review.
1980
Hypertrophy and increased glial fibrillary acidic protein are coupled to increased protection against cytotoxicity in glioma cell lines.
1998 Apr
Scope and mechanism of intramolecular aziridination of cyclopent-3-enyl-methylamines to 1-azatricyclo[2.2.1.0(2,6)]heptanes with lead tetraacetate.
2009 Aug 26
Coordinated waves of gene expression during neuronal differentiation of embryonic stem cells as basis for novel approaches to developmental neurotoxicity testing.
2011 Mar
The protective effect of flaxseed oil on lead acetate-induced renal toxicity in rats.
2011 Oct 30
Patents

Sample Use Guides

In Vivo Use Guide
Unknown
Route of Administration: Unknown
It was examined the associations of increased glial fibrillary acidic protein (GFAP) levels and hypertrophie changes with susceptibility to toxic insult in C6 rat glioma cells. The cells were treated with serial pulses of dibutyryl-cAMP (dBcAMP) (each 48 hr) which increased levels of GFAP approximately twofold and the surface to volume ratio by approximately 1.7 times after the third pulse. This treatment reduced cell number by 22% and increased total protein by 10%. The cells were then exposed to different toxic substances [tin chloride, lead tetraacetate, chloroquine, cadmium chloride, aluminium chloride, mercuric chloride, acrylamide, triethyltin bromide, ethylenediaminetetraacetatic acid (EDTA)] and toxicity to the cells measured by the neutral red (NR) assay. With the exceptions of aluminium chloride and EDTA, 50% effective concentration (EC(50)) values for the toxic substances were increased up to 10,000 times (for cadmium chloride).
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:33:15 GMT 2023
Edited
by admin
on Fri Dec 15 16:33:15 GMT 2023
Record UNII
KL498O6790
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LEAD ACETATE ANHYDROUS
Common Name English
NSC-75797
Code English
SALT OF SATURN
Common Name English
NEUTRAL LEAD ACETATE
Common Name English
ACETIC ACID LEAD(2+) SALT (2:1)
Common Name English
SUGAR OF LEAD
Common Name English
PLUMBOUS ACETATE
Common Name English
LEAD(II) ACETATE
Systematic Name English
LEAD ACETATE [HSDB]
Common Name English
PLUMBUM ACETICUM [HPUS]
Common Name English
PLUMBUM ACETICUM
HPUS  
Common Name English
LEAD ACETATE [MI]
Common Name English
Lead acetate [WHO-DD]
Common Name English
Code System Code Type Description
DAILYMED
KL498O6790
Created by admin on Fri Dec 15 16:33:15 GMT 2023 , Edited by admin on Fri Dec 15 16:33:15 GMT 2023
PRIMARY
MERCK INDEX
m6722
Created by admin on Fri Dec 15 16:33:15 GMT 2023 , Edited by admin on Fri Dec 15 16:33:15 GMT 2023
PRIMARY Merck Index
PUBCHEM
57351453
Created by admin on Fri Dec 15 16:33:15 GMT 2023 , Edited by admin on Fri Dec 15 16:33:15 GMT 2023
PRIMARY
WIKIPEDIA
LEAD(II) ACETATE
Created by admin on Fri Dec 15 16:33:15 GMT 2023 , Edited by admin on Fri Dec 15 16:33:15 GMT 2023
PRIMARY
NSC
75797
Created by admin on Fri Dec 15 16:33:15 GMT 2023 , Edited by admin on Fri Dec 15 16:33:15 GMT 2023
PRIMARY
FDA UNII
KL498O6790
Created by admin on Fri Dec 15 16:33:15 GMT 2023 , Edited by admin on Fri Dec 15 16:33:15 GMT 2023
PRIMARY
CHEBI
31767
Created by admin on Fri Dec 15 16:33:15 GMT 2023 , Edited by admin on Fri Dec 15 16:33:15 GMT 2023
PRIMARY
CAS
301-04-2
Created by admin on Fri Dec 15 16:33:15 GMT 2023 , Edited by admin on Fri Dec 15 16:33:15 GMT 2023
PRIMARY
ECHA (EC/EINECS)
206-104-4
Created by admin on Fri Dec 15 16:33:15 GMT 2023 , Edited by admin on Fri Dec 15 16:33:15 GMT 2023
PRIMARY
RXCUI
1544391
Created by admin on Fri Dec 15 16:33:15 GMT 2023 , Edited by admin on Fri Dec 15 16:33:15 GMT 2023
PRIMARY RxNorm
HSDB
1404
Created by admin on Fri Dec 15 16:33:15 GMT 2023 , Edited by admin on Fri Dec 15 16:33:15 GMT 2023
PRIMARY
EPA CompTox
DTXSID6020773
Created by admin on Fri Dec 15 16:33:15 GMT 2023 , Edited by admin on Fri Dec 15 16:33:15 GMT 2023
PRIMARY
Related Record Type Details
SOLVATE->ANHYDROUS
SOLVATE->ANHYDROUS