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Zinc nitrate
Zinc nitrate
Zinc nitrate
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Zinc nitrate
Zinc nitrate
Zinc nitrate
Names
IUPAC name
Zinc nitrate
Other names
Zinc dinitrate
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard 100.029.038 Edit this at Wikidata
EC Number
  • 231-943-8
RTECS number
  • ZH4772000
UNII
UN number 1514
  • InChI=1S/2NO3.Zn/c2*2-1(3)4;/q2*-1;+2 checkY
    Key: ONDPHDOFVYQSGI-UHFFFAOYSA-N checkY
  • InChI=1/2NO3.Zn/c2*2-1(3)4;/q2*-1;+2
    Key: ONDPHDOFVYQSGI-UHFFFAOYAQ
  • [N+](=O)([O-])[O-].[N+](=O)([O-])[O-].[Zn+2]
Properties
Zn(NO3)2
Molar mass 189.36 g/mol (anhydrous)
297.49 g/mol (hexahydrate)
Appearance colorless, deliquescent crystals
Density 2.065 g/cm3 (hexahydrate)
Melting point 110 °C (230 °F; 383 K) (anhydrous)
45.5 °C (trihydrate)
36.4 °C (hexahydrate)
Boiling point ~ 125 °C (257 °F; 398 K) decomposes (hexahydrate)
327 g/(100 mL), 40 °C (trihydrate)
184.3 g/(100 mL), 20 °C (hexahydrate)
Solubility very soluble in alcohol
−63.0·10−6 cm3/mol
Hazards
Occupational safety and health (OHS/OSH):
Main hazards
 Oxidant, may explode on heating
GHS labelling:
GHS03: OxidizingGHS07: Exclamation mark
Flash point Non-flammable
Safety data sheet (SDS) ICSC 1206
Related compounds
Other anions
 Zinc sulfate
Zinc chloride
Other cations
 Cadmium nitrate
Mercury(II) nitrate
Related compounds
 Copper(II) nitrate
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)

Zinc nitrate is an inorganic chemical compound with the formula Zn(NO3)2. This colorless, crystalline salt is highly deliquescent. It is typically encountered as a hexahydrate Zn(NO3)2·6H2O. It is soluble in both water and alcohol.

Synthesis

[edit]

Zinc nitrate is usually prepared by dissolving zinc metal, zinc oxide, or related materials in nitric acid:

Zn + 2 HNO3 → Zn(NO3)2 + H2
ZnO + 2 HNO3 → Zn(NO3)2 + H2O

These reactions are accompanied by the hydration of the zinc nitrate.

The anhydrous salt arises by the reaction of anhydrous zinc chloride with nitrogen dioxide:[1]

ZnCl2 + 4 NO2 → Zn(NO3)2 + 2 NOCl

Reactions

[edit]

Treatment of zinc nitrate with acetic anhydride gives zinc acetate.[2]

On heating, zinc nitrate undergoes thermal decomposition to form zinc oxide, nitrogen dioxide and oxygen:

2 Zn(NO3)2 → 2 ZnO + 4 NO2 + 1 O2

Aqueous zinc nitrate contains aquo complexes [Zn(H2O)6]2+ and [Zn(H2O)4]2+.[3] and, thus, this reaction may be better written as the reaction of the aquated ion with hydroxide through donation of a proton, as follows.

Applications

[edit]

Zinc nitrate has no large scale application but is used on a laboratory scale for the synthesis of coordination polymers.[4] Its controlled decomposition to zinc oxide has also been used for the generation of various ZnO based structures, including nanowires.[5]

It is used as a corrosion inhibitor. [6]


It can be used as a mordant in dyeing. An example reaction gives a precipitate of zinc carbonate:

Zn(NO3)2 + Na2CO3 → ZnCO3 + 2 NaNO3

References

[edit]
Revisions and contributorsEdit on WikipediaRead on Wikipedia

Zinc nitrate

View on Grokipedia
from Grokipedia
Zinc nitrate is an inorganic compound with the chemical formula Zn(NO₃)₂, consisting of zinc cations and nitrate anions, and it typically appears as a colorless crystalline solid or white powder. It is highly soluble in water, with the hexahydrate form Zn(NO₃)₂·6H₂O exhibiting solubility of approximately 184 g/100 mL at 20 °C, and it is also soluble in alcohol. The compound has a molecular weight of 189.4 g/mol for the anhydrous form and melts at around 36–110 °C depending on the hydration state. Zinc nitrate is commonly prepared by the reaction of metal or with . In industrial and chemical applications, it serves as a catalyst for the synthesis of various organic compounds and in the production of other chemicals, as well as a in processes to fix colors onto fabrics. It is also utilized as a coagulant in production, an analytical for determination, and a precursor for nanoparticles employed in and synthesis. Emerging as of 2025 explores its use in rechargeable zinc-nitrate batteries for and electrocatalytic nitrate reduction to . Additionally, nitrate acts as a source of in fertilizers, medicines, and dyes, contributing to its role in and pharmaceuticals. As a strong , zinc nitrate can accelerate combustion and release toxic oxides when heated or involved in fires, posing significant hazards including risks when mixed with combustible materials. It is irritating to the skin, eyes, and , and proper handling requires protective measures to mitigate and environmental impacts on aquatic life.

General properties

Chemical identity

Zinc nitrate is an with the Zn(NO3)2Zn(NO_3)_2 for the form. The of the zinc nitrate is 189.4 g/mol. It is systematically named zinc dinitrate. Common names for the compound include zinc nitrate. The compound is most commonly encountered as the hexahydrate, Zn(NO3)2⋅6H2OZn(NO_3)_2 \cdot 6H_2O, which has a of 297.5 g/mol. This hydrated form is referred to as zinc nitrate hexahydrate. The hexahydrate is the stable form at . Zinc nitrate consists of Zn2+Zn^{2+} cations and NO3−NO_3^- anions arranged in an ionic crystalline lattice. In the hexahydrate, six molecules are incorporated into the structure. The crystal structure of the hexahydrate is orthorhombic, belonging to the Pnma.

Physical characteristics

Zinc nitrate is typically encountered as the hexahydrate, Zn(NO₃)₂·6H₂O, which appears as colorless, transparent, deliquescent crystals that are highly hygroscopic, readily absorbing moisture from the air and potentially dissolving into a state upon exposure. is odorless, with no characteristic taste noted due to its . The density of the hexahydrate is 2.065 g/cm³ at 15–20 °C. It has a low of 36.4 °C for the hexahydrate, while the anhydrous form melts at approximately 110 °C but decomposes before fully . Zinc nitrate decomposes upon heating before reaching a , exhibiting no stable vapor phase. Zinc nitrate demonstrates high in , with the hexahydrate dissolving at approximately 184–200 g per 100 mL at 20 °C, attributed to its ionic composition facilitating strong hydration interactions. It is also soluble in and but insoluble in organic solvents such as acetone.

Synthesis

Laboratory preparation

Zinc nitrate is primarily prepared in the laboratory by dissolving metal in dilute at , which produces gas as a byproduct. The reaction follows the equation
\ceZn+2HNO3−>Zn(NO3)2+H2\ce{Zn + 2 HNO3 -> Zn(NO3)2 + H2}
and requires careful control of the acid concentration to prevent side reactions, such as the evolution of nitrogen oxides (NO_x) that can occur with more concentrated acid. This method is straightforward and suitable for educational settings, as the reaction proceeds vigorously but controllably under ambient conditions. An alternative laboratory synthesis involves the reaction of zinc oxide with , which is an acid-base neutralization yielding as the byproduct. The balanced equation is
\ceZnO+2HNO3−>Zn(NO3)2+H2O\ce{ZnO + 2 HNO3 -> Zn(NO3)2 + H2O}
and typically requires gentle heating to achieve complete dissolution of the relatively insoluble zinc oxide. This approach is useful when starting from zinc oxide, a common precursor, and avoids the generation of gas. Following synthesis, purification is achieved by evaporating the to induce of the hexahydrate form, Zn(NO₃)₂·6H₂O, which is the stable solid at due to its high in . For the anhydrous compound, the hexahydrate is subjected to under or in a with a hygroscopic agent to remove coordinated molecules without . These reactions generally afford high yields when acid concentration and reaction conditions are optimized to minimize losses from side products.

Industrial production

Zinc nitrate is produced industrially by reacting metal or oxide with , following the same reactions as in laboratory preparation but on a large scale. This production often utilizes excess in manufacturing facilities, where metallic or zinc scraps are reacted to form solutions such as 50% zinc nitrate (containing 17% Zn). Resource recovery methods involve leaching zinc-containing wastes, such as spent catalysts, with (typically 1-3 M) at controlled temperatures (around 60-80°C) to achieve extraction efficiencies exceeding 90%, yielding concentrated zinc nitrate solutions suitable for further processing. An alternative method involves the neutralization of with . The reaction proceeds as: \ceZn(OH)2+2HNO3−>Zn(NO3)2+2H2O\ce{Zn(OH)2 + 2 HNO3 -> Zn(NO3)2 + 2 H2O} Post-reaction, the solutions are concentrated via evaporation or distillation under vacuum to achieve desired viscosities, typically removing water to form hexahydrate crystals or solutions for commercial use. Zinc nitrate is produced primarily as a specialty chemical with a market value around USD 150-200 million as of 2023. Quality control ensures commercial grades meet purity standards of 98-99% for general industrial use, rising to over 99.5% for catalytic applications, verified through assays for insoluble matter, chlorides, sulfates, and heavy metals like iron (limited to 0.01% max).

Chemical reactivity

Thermal decomposition

Zinc nitrate undergoes upon heating, primarily yielding zinc oxide as the solid residue along with and oxygen gases. The overall balanced reaction for the anhydrous form is 2Zn(NO3)2→2ZnO+4NO2+O22 \mathrm{Zn(NO_3)_2} \rightarrow 2 \mathrm{ZnO} + 4 \mathrm{NO_2} + \mathrm{O_2}. This is endothermic, as indicated by endothermic peaks in (DTA) profiles. For the common hexahydrate form, Zn(NO3)2⋅6H2O\mathrm{Zn(NO_3)_2 \cdot 6H_2O}, decomposition begins with dehydration and partial hydrolysis at lower temperatures, forming intermediate basic zinc nitrates. Thermogravimetric (TG) and DTA studies show an initial stage starting around 115°C, where water loss and hydroxide formation lead to a layered structure of Zn(NO3)2⋅2Zn(OH)2\mathrm{Zn(NO_3)_2 \cdot 2Zn(OH)_2}. Subsequent dehydroxylation occurs between 200°C and 235°C, producing Zn(NO3)2⋅2ZnO\mathrm{Zn(NO_3)_2 \cdot 2ZnO}, followed by denitration of the nitrate groups between 290°C and 350°C, ultimately forming ZnO. The anhydrous Zn(NO3)2\mathrm{Zn(NO_3)_2} decomposes at higher temperatures, with the onset around 236°C and major nitrate breakdown near 312°C, as detected by electron spin resonance (ESR) monitoring of nitrogen peroxide species. Mass spectrometry confirms the evolution of NO2\mathrm{NO_2} and O2\mathrm{O_2} during denitration, with nitrate reduction pathways involving oxygen release before complete water elimination. The temperature dependence is evident from DTA data, which reveal overlapping endothermic peaks for and exothermic contributions from in air, with the process shifting to higher temperatures under inert atmospheres like . The zinc oxide residue is a fine, crystalline powder suitable for applications due to its high purity and stability. Additionally, controlled of zinc nitrate serves as a straightforward method to produce pure ZnO nanoparticles, often achieved by heating the hexahydrate at 500°C in air for 2 hours, yielding particles with applications in . The gaseous byproducts, primarily NOx\mathrm{NO_x} species, evolve progressively from 240°C onward.

Reactions with reagents

Zinc nitrate reacts with aqueous bases such as to produce a white gelatinous precipitate of , according to the equation: \ceZn(NO3)2+2NaOH−>Zn(OH)2v+2NaNO3\ce{Zn(NO3)2 + 2 NaOH -> Zn(OH)2 v + 2 NaNO3} The formed is amphoteric, dissolving in excess to yield the soluble , \ce[Zn(OH)4]2−\ce{[Zn(OH)4]^2-}. Treatment of zinc nitrate with organic anhydrides, such as , yields along with derivatives. This transformation is a key method for preparing and leverages zinc nitrate's role in facilitating esterification processes through catalytic activation. In the presence of excess , zinc nitrate undergoes coordination to form the stable tetraamminezinc(II) nitrate complex: \ceZn(NO3)2+4NH3−>[Zn(NH3)4](NO3)2\ce{Zn(NO3)2 + 4 NH3 -> [Zn(NH3)4](NO3)2} This tetrahedral complex exemplifies zinc(II)'s tendency to form ammine ligands, with the reaction proceeding in aqueous or alcoholic media under mild conditions. As a Lewis acid, zinc nitrate catalyzes aromatic nitration reactions by coordinating with nitric acid to generate the electrophilic nitronium ion (\ceNO2+\ce{NO2+}) for substitution on activated aromatic rings, such as phenols or anilines. For instance, it promotes regioselective mononitration when combined with nitric acid under controlled conditions, enhancing reaction efficiency over traditional mixed-acid systems. Zinc nitrate participates in reactions with strong reducing agents like , leading to the reduction of Zn(II) to metallic , often as zero-valent nanoparticles: \ceZn(NO3)2+2NaBH4+6H2O−>Zn+2NaNO3+2B(OH)3+7H2\ce{Zn(NO3)2 + 2 NaBH4 + 6 H2O -> Zn + 2 NaNO3 + 2 B(OH)3 + 7 H2} This process typically requires inert atmospheres to prevent oxidation and is utilized in nanomaterial synthesis, where the particle size depends on reaction parameters like and .

Applications

Industrial uses

In the , zinc nitrate functions as a to fix onto fabrics, forming stable coordination complexes with materials that improve color adhesion and durability. This role ensures uniform dye uptake and resistance to during washing or exposure to light, making it valuable for producing high-quality colored textiles. Zinc nitrate is incorporated as a in protective coatings and paints applied to metals, where it helps prevent oxidation and formation on surfaces such as machinery and structural components. Typical formulations include it at low concentrations to provide passivation without altering the coating's aesthetic or mechanical properties. As a source of essential zinc micronutrients, zinc nitrate is added to nitrate-based fertilizers to address soil deficiencies and promote growth in agricultural settings. It supports activation and protein synthesis in crops, contributing to improved yields in zinc-limited regions without introducing excess nitrates that could harm the environment. In ceramics and , zinc nitrate is used as a precursor to incorporate in advanced glazes and coatings, contributing to enhanced properties such as photocatalytic activity. Its Lewis acid properties underpin many of these catalytic applications by enabling coordination with substrates to lower activation energies in reactions.

Research applications

Zinc nitrate serves as a versatile precursor in the synthesis of zinc oxide (ZnO) nanomaterials, particularly for the fabrication of ZnO nanowires through thermal decomposition processes integrated with vapor transport methods. In these approaches, zinc nitrate is thermally decomposed to generate zinc oxide vapor, which is then transported and condensed onto substrates to form aligned nanowires with controlled morphology and high aspect ratios. This method enables the production of high-quality, single-crystalline ZnO nanowires suitable for optoelectronic applications, such as UV sensors and light-emitting devices, due to their enhanced surface area and quantum confinement effects. In the development of coordination polymers, zinc nitrate acts as a metal source and template for constructing metal-organic frameworks (MOFs) incorporating ligands, which exhibit promising capabilities for gas storage. These frameworks, synthesized via solvothermal reactions with organic linkers like , demonstrate selective adsorption of over other gases, attributed to the coordination of ions that tune pore size and surface polarity. Such Zn-based MOFs have shown CO2 uptake of approximately 0.8 mmol/g at 273 K, positioning them as candidates for carbon capture technologies in energy research. As a catalyst in , zinc nitrate and its derivatives, such as nitrate, provide a non-toxic alternative in protocols for reactions like esterification and . In solvent-free esterification of fatty acids with alcohols, nitrate—derived from zinc nitrate—achieves high yields (over 90%) under mild conditions, promoting by avoiding hazardous acids and enabling catalyst recyclability up to five cycles without significant activity loss. Similarly, in processes, zinc nitrate facilitates the incorporation of CO into organic substrates, enhancing reaction efficiency in eco-friendly media while minimizing waste generation. In biomedical research, zinc nitrate functions as a source for formulating agents within systems, often through its conversion to ZnO nanoparticles integrated into carriers like hydrogels or liposomes. These systems leverage the release of Zn²⁺ ions to disrupt bacterial cell membranes and generate , achieving broad-spectrum efficacy against pathogens such as and with minimum inhibitory concentrations as low as 0.5 mg/mL. Such constructs have been explored for dressings and targeted therapies, where controlled zinc release enhances and reduces resistance development. Electrochemical studies of nitrate highlight its role in electrolytes for zinc-ion batteries, where it provides Zn²⁺ ions in aqueous or polymer matrices to improve ionic conductivity and cycling stability. In biopolymer-based electrolytes, such as pectin- nitrate composites, conductivities reach 1.2 × 10⁻³ S/cm at , enabling reversible zinc plating/stripping with capacities exceeding 200 mAh/g over 500 cycles. The anion's weak with Zn²⁺ mitigates formation and hydrogen evolution, advancing the development of safe, high-performance devices.

Safety and environmental considerations

Health hazards

Zinc nitrate poses significant health risks primarily through direct exposure routes, acting as an irritant and potential due to its content and oxidizing ions. of zinc nitrate dust or vapors can irritate the , leading to symptoms such as coughing, , and throat discomfort. Prolonged or high-level exposure to compounds, including zinc nitrate, is associated with when heated materials release zinc oxide fumes, characterized by flu-like symptoms including fever, chills, muscle aches, and fatigue that typically resolve within 24-48 hours. Occupational exposure limits for compounds are set at 5 mg/m³ as an 8-hour time-weighted average to mitigate these risks. Contact with zinc nitrate can cause severe irritation or burns to the skin and eyes, owing to its corrosive nature from the acidic properties of the nitrate component in aqueous solutions. Skin exposure may result in redness, pain, and , while eye contact can lead to serious damage, including and potential vision impairment if not promptly treated. of zinc nitrate is harmful, potentially causing gastrointestinal distress such as , , , and , along with symptoms of zinc poisoning like metallic taste and . The oral LD50 in rats is approximately 1,190-2,000 mg/kg, indicating moderate . Chronic exposure to zinc nitrate may lead to zinc overload, which can impair immune function, cause anemia, and affect copper absorption, potentially resulting in neurological effects over time. Under the Globally Harmonized System (GHS), zinc nitrate is classified as a skin irritant (H315), causing serious eye irritation (H319), and a respiratory irritant (H335). Its oxidizing properties can exacerbate injury risks in fire scenarios by intensifying combustion and releasing hazardous fumes. To prevent health hazards, such as chemical-resistant gloves, safety goggles, and respirators should be used during handling. Zinc nitrate should be stored in a cool, dry, well-ventilated area away from incompatibles like reducing agents. In case of exposure, includes flushing eyes or skin with copious water for at least 15 minutes, seeking medical attention for or , and moving to fresh air for respiratory incidents.

Ecological impact

Zinc nitrate dissociates in aqueous environments into zinc ions (Zn²⁺) and nitrate ions (NO₃⁻), both of which contribute to its ecological impacts. The compound exhibits high to aquatic organisms, primarily driven by the component. For instance, the 96-hour LC50 for fish exposed to zinc nitrate is reported as low as 0.112 mg/L, classifying it as very toxic to aquatic life under GHS criteria (Aquatic Acute 1). Additionally, nitrate ions from zinc nitrate can promote in surface waters by stimulating excessive algal growth, leading to oxygen depletion and harm to aquatic ecosystems. Zinc ions from zinc nitrate readily bioaccumulate in sediments and aquatic organisms, where they bind to particulate matter and organic sediments, reducing but concentrating in benthic communities. factors for in freshwater and range from 200 to 2000 mg/kg dry weight, depending on exposure conditions like and hardness, though through food chains is limited due to regulatory mechanisms in higher trophic levels. In contrast, ions are highly mobile and prone to leaching into , potentially contaminating aquifers and exacerbating in downstream ecosystems. Regarding persistence, the nitrate component of is subject to microbial in aerobic and anaerobic aquatic systems, with environmental half-lives typically ranging from days to weeks under favorable conditions, rendering it readily biodegradable. However, ions persist indefinitely as an elemental form, undergoing no degradation but transforming through (e.g., as ZnCO₃ or ZnS) or adsorption to sediments, with residence times in water bodies extending from months to years based on geochemical factors like and . Under global harmonized system (GHS) classifications, zinc nitrate is designated as hazardous to the environment with hazard statements H400 (very toxic to aquatic life) and H411 (toxic to aquatic life with long-lasting effects), reflecting its potential for widespread ecological disruption. In the , REACH registration requires risk assessments for emissions, and wastewater discharge is regulated under the Urban Waste Water Treatment Directive (91/271/EEC), which mandates treatment to limit zinc concentrations below standards (typically 10-50 µg/L for inland waters) to prevent sediment accumulation and . Mitigation strategies for zinc nitrate releases focus on industrial treatment, where as (via adjustment to 8-10) or effectively removes over 99% of dissolved zinc before discharge, minimizing aquatic exposure. In soil remediation contexts, controlled application of zinc nitrate serves as a source to address deficiencies in agricultural lands, but excessive use risks overload, leading to and reduced microbial diversity at concentrations exceeding 300 mg/kg.

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