Details
Stereochemistry | ACHIRAL |
Molecular Formula | 2CHO2.Zn |
Molecular Weight | 155.444 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[Zn++].[O-]C=O.[O-]C=O
InChI
InChIKey=XOBMCBQSUCOAOC-UHFFFAOYSA-L
InChI=1S/2CH2O2.Zn/c2*2-1-3;/h2*1H,(H,2,3);/q;;+2/p-2
Molecular Formula | CHO2 |
Molecular Weight | 45.0174 |
Charge | -1 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Molecular Formula | Zn |
Molecular Weight | 65.409 |
Charge | 2 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Zinc formate is a white crystalline solid. It is soluble in water. The primary hazard is the threat to the environment. Immediate steps should be taken to limit its spread to the environment. It is used as a catalyst in chemical processing and as a waterproofing agent. Zinc formate is used as a pharmaceutical intermediate. Synthetic and plant-derived zinc formate were equally effective as inhibitors of cytochrome P-450 enzymes and as hepatoprotective agents in carbon tetrachloride-treated rats.
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: Cytochrome P-450, rat Sources: https://www.ncbi.nlm.nih.gov/pubmed/8583799 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Primary | Unknown Approved UseUnknown |
PubMed
Title | Date | PubMed |
---|---|---|
Theoretical Study on the Mechanism of Formation of Cyanate Resins. | 1999 Jun 25 |
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Solvent effects on the structural and formyl substrate reactivity properties of a nitrogen/sulfur-ligated zinc hydroxide complex. | 2006 May 15 |
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Systematic first principles parameterization of force fields for metal-organic frameworks using a genetic algorithm approach. | 2009 Feb 5 |
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Raman and IR studies of pressure- and temperature-induced phase transitions in [(CH2)3NH2][Zn(HCOO)3]. | 2014 Dec 1 |
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Mononuclear Phenolate Diamine Zinc Hydride Complexes and Their Reactions With CO(2). | 2014 Mar 10 |
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Temperature- and pressure-dependent studies of niccolite-type formate frameworks of [NH(3)(CH(2))(4)NH(3)][M(2)(HCOO)(6)] (M = Zn, Co, Fe). | 2016 Oct 5 |
Patents
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/8583799
Rats: Groups of 3 rats were administered 1 ml of water or 10 mg/ml zinc formate solution daily by gastric lavage for 3 days.
Route of Administration:
Other
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/8583799
Zinc formate (0.25 - 2.50 mg/ml) dose-dependently inhibited rat liver microsomal aminopyrine-N-demethylase activity.
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 04:18:41 GMT 2023
by
admin
on
Sat Dec 16 04:18:41 GMT 2023
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Record UNII |
ZZ67G2CT75
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Record Status |
Validated (UNII)
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Record Version |
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EPA PESTICIDE CODE |
87802
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