U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula 2C2H3O2.Pb.3H2O
Molecular Weight 379.3
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LEAD ACETATE

SMILES

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

InChI

InChIKey=YCFCGUGOMKHROF-UHFFFAOYSA-L
InChI=1S/2C2H4O2.3H2O.Pb.2H/c2*1-2(3)4;;;;;;/h2*1H3,(H,3,4);3*1H2;;;/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 H2O
Molecular Weight 18.0153
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C2H4O2
Molecular Weight 60.052
Charge 0
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
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
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 15:04:24 GMT 2023
Edited
by admin
on Fri Dec 15 15:04:24 GMT 2023
Record UNII
RX077P88RY
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LEAD ACETATE
INCI   JAN   VANDF  
INCI  
Official Name English
LEAD ACETATE [INCI]
Common Name English
LEAD ACETATE TRIHYDRATE [MI]
Common Name English
LEAD ACETATE [VANDF]
Common Name English
LEAD ACETATE TRIHYDRATE
MI  
Systematic Name English
LEAD(II) ACETATE TRIHYDRATE
Systematic Name English
LEAD(2+) DIACETATE TRIHYDRATE
Systematic Name English
LEAD ACETATE [JAN]
Common Name English
Classification Tree Code System Code
EPA PESTICIDE CODE 48001
Created by admin on Fri Dec 15 15:04:24 GMT 2023 , Edited by admin on Fri Dec 15 15:04:24 GMT 2023
Code System Code Type Description
PUBCHEM
134688182
Created by admin on Fri Dec 15 15:04:24 GMT 2023 , Edited by admin on Fri Dec 15 15:04:24 GMT 2023
PRIMARY
MERCK INDEX
m6722
Created by admin on Fri Dec 15 15:04:24 GMT 2023 , Edited by admin on Fri Dec 15 15:04:24 GMT 2023
PRIMARY Merck Index
MESH
C008261
Created by admin on Fri Dec 15 15:04:24 GMT 2023 , Edited by admin on Fri Dec 15 15:04:24 GMT 2023
PRIMARY
RXCUI
1423667
Created by admin on Fri Dec 15 15:04:24 GMT 2023 , Edited by admin on Fri Dec 15 15:04:24 GMT 2023
PRIMARY RxNorm
DAILYMED
RX077P88RY
Created by admin on Fri Dec 15 15:04:24 GMT 2023 , Edited by admin on Fri Dec 15 15:04:24 GMT 2023
PRIMARY
FDA UNII
RX077P88RY
Created by admin on Fri Dec 15 15:04:24 GMT 2023 , Edited by admin on Fri Dec 15 15:04:24 GMT 2023
PRIMARY
CAS
6080-56-4
Created by admin on Fri Dec 15 15:04:24 GMT 2023 , Edited by admin on Fri Dec 15 15:04:24 GMT 2023
PRIMARY
CHEBI
33112
Created by admin on Fri Dec 15 15:04:24 GMT 2023 , Edited by admin on Fri Dec 15 15:04:24 GMT 2023
PRIMARY
CHEBI
31767
Created by admin on Fri Dec 15 15:04:24 GMT 2023 , Edited by admin on Fri Dec 15 15:04:24 GMT 2023
PRIMARY
SMS_ID
100000077101
Created by admin on Fri Dec 15 15:04:24 GMT 2023 , Edited by admin on Fri Dec 15 15:04:24 GMT 2023
PRIMARY
EPA CompTox
DTXSID3031521
Created by admin on Fri Dec 15 15:04:24 GMT 2023 , Edited by admin on Fri Dec 15 15:04:24 GMT 2023
PRIMARY
EVMPD
SUB14335MIG
Created by admin on Fri Dec 15 15:04:24 GMT 2023 , Edited by admin on Fri Dec 15 15:04:24 GMT 2023
PRIMARY
Related Record Type Details
ANHYDROUS->SOLVATE
Related Record Type Details
ACTIVE MOIETY