Lead(II) formate - ≥90% , CAS No.811-54-1

CAS: 811-54-1 Cat. No.: L335828 Molecular Weight: 297.23 EC Number: 212-371-8
AVAILABLE TO ORDER
GRADE & PURITY ≥90%
Synonyms
DTXSID2061145 | Lead formate Pb(O2CH)2 | Lead diformate | EINECS 212-371-8 | EINECS 230-336-5 | Formic acid lead(2+) salt (2:1) | Lead formate (Pb(HCO2)2) | NSC-112233 | Formic acid,lead salt | LEAD(II) FORMATE | Formic acid, lead(2+) salt | Formic acid,
Storage
Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
10g
L335828-10g
3
$28.90
50g
L335828-50g
3
$82.90
Enter a quantity for the sizes you want to add.
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Why this grade

≥90% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature Ships Normal Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 3 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Synonyms
DTXSID2061145 | Lead formate Pb(O2CH)2 | Lead diformate | EINECS 212-371-8 | EINECS 230-336-5 | Formic acid lead(2+) salt (2:1) | Lead formate (Pb(HCO2)2) | NSC-112233 | Formic acid, lead salt | LEAD(II) FORMATE | Formic acid, lead(2+) salt | Formic acid,
Specifications & Purity
≥90%
Storage
Room temperature
Shipped In
Normal
Purity
≥90%
Names and Identifiers
Pubchem Sid504753752
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504753752
Canonical SmilesC(=O)[O-].C(=O)[O-].[Pb+2]
IUPAC Namelead(2+);diformate
InChIKeyZGVSCHRFRACEIO-UHFFFAOYSA-L
INCHI1S/2CH2O2.Pb/c2*2-1-3;/h2*1H,(H,2,3);/q;;+2/p-2
Isomeric SMILES C(=O)[O-].C(=O)[O-].[Pb+2]
UN Number 2291
Packing Group III
Molecular Weight 297.23
Reaxy-Rn 3688908
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3688908&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic acids and derivatives
ClassCarboxylic acids and derivatives
SubclassCarboxylic acids
Intermediate Tree Nodes Not available
Direct ParentCarboxylic acids
Alternative Parents Monocarboxylic acids and derivatives  Organic salts  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkNot available
Substituents Monocarboxylic acid or derivatives - Carboxylic acid - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organic salt - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound
DescriptionThis compound belongs to the class of organic compounds known as carboxylic acids. These are compounds containing a carboxylic acid group with the formula -C(=O)OH.
External Descriptors Not available
3D Structure
Interactive Chemical Structure Model





Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

2 results found

Lot NumberCertificate TypeDateItem
H2218619Certificate of AnalysisJun 10, 2025 L335828
H2218621Certificate of AnalysisJun 10, 2025 L335828
Chemical and Physical Properties
SolubilitySoluble in water (16 mg/ml at 20 °C).
Boil Point(°C)100.6° C at 760 mmHg (Predicted)
Melt Point(°C)190° C
Molecular Weight297.000 g/mol
XLogP3
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count4
Rotatable Bond Count0
Exact Mass297.972 Da
Monoisotopic Mass297.972 Da
Topological Polar Surface Area80.300 Ų
Heavy Atom Count7
Formal Charge0
Complexity7.500
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count3
Citations of This Product
References
1. Bin Zou, Yangping Zhang, Fei Gao, Zhuolin Li, Caiqin Wang, Zhengying Wu, Dongqiong Wang, Yukou Du.  (2022)  3D PdPb nanochain networks with efficient catalytic performance for ethylene glycol electrooxidation.  INTERNATIONAL JOURNAL OF HYDROGEN ENERGY,      [PMID:] [10.1016/j.ijhydene.2022.07.207]
2. Bo-Qiang Miao, Zi-Han Yuan, Xi-Lai Liu, Xuan Ai, Guang-Tao Zhao, Pei Chen, Pu-Jun Jin, Yu Chen.  (2024)  Tensile Strain and Interatomic Orbital Hybridization Effects Boost the Electrocatalytic Performance of Intermetallic Pd3Pb Nanowires for Ethanol Electrooxidation†.  CHINESE JOURNAL OF CHEMISTRY,      [PMID:] [10.1002/cjoc.202400450]
3. Yonghui Ye, Yu Zhang, Xintong Yan, Gong Ning, Shi Hu.  (2025)  Pb–Pd alloy catalysts with intercalated Pb atoms: optimized electronic and lattice structures for enhanced electrochemical ethanol oxidation.  DALTON TRANSACTIONS,      [PMID:40192190] [10.1039/D5DT00117J]
Solution Calculators
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