Backtracking through the development of cupric sulfide sparks images of early chemists rummaging through minerals in search of something useful. Ancient miners and metalwork artisans probably struck upon this compound, even if they didn’t name it as we do today. Later, as the discipline of chemistry took shape throughout the 18th and 19th centuries, a clearer understanding of metal sulfides like CuS grew with advances in analytical techniques. Laboratory synthesis replaced mineral extraction, granting easy access to cupric sulfide for researchers analyzing its characteristic dark blue-black shimmer. The shift from natural mineral covellite toward controlled production marked a key milestone, paving the way for wider industrial and scientific use.
Cupric sulfide stands out as a reliable laboratory staple and manufacturing input. Known under trade names such as copper(II) sulfide and Covellite (especially when referring to its natural mineral form), the compound sees distribution as a fine powder. Both academic and industrial buyers value its predictable composition: copper locked together with sulfur in a straightforward 1:1 atomic arrangement. Packaging usually features easy-to-read hazard and content labels, as regulations demand clear communication for chemical handling. Today, cupric sulfide finds places in research labs, electronics manufacturing, and pigment production, cementing its versatility.
Anybody who has seen cupric sulfide under a microscope can’t miss its striking color. The substance sports a deep blue-black appearance, reflecting its structure where every copper atom nestles next to a sulfur neighbor. It feels smooth and fine when handled with gloves, yet clumps if exposed to moisture. With a melting point that exceeds 500°C and negligible solubility in water, CuS refuses to dissolve or burn away easily. Its density, close to 4.6 g/cm³, gives it a heavy feel for those accustomed to lighter powders. Chemically, cupric sulfide shows only a modest willingness to react unless pushed with strong acids or oxidizers. This stubbornness keeps it stable in closed containers over years, reassuring both buyers and long-term users.
Laboratory suppliers offer detailed technical sheets for cupric sulfide, listing properties such as purity (usually above 99%), particle size every few microns, and trace metal content. These details serve not just as quality assurance but help project planners ensure the material fits the purpose. Safety data, traceability codes, and handling directions support users from shipment through end-of-life disposal. Manufacturers typically label containers with well-known synonyms, batch lot information, and international regulatory identifiers, minimizing confusion and smoothing audits. One-size-fits-all labeling rarely meets these standards in practice; I’ve seen how custom spec sheets delivered to research labs or electronics lines make traceability easier.
Old textbooks taught apprentices to mix copper salts such as copper(II) sulfate or copper(II) chloride with hydrogen sulfide gas, yielding cupric sulfide as a solid byproduct. Today, chemical engineers fine-tune these reactions, sometimes bubbling H2S through copper(II) salt solutions under controlled pH and temperature. Excess sulfur or secondary purification stages weed out unwanted phases or trace metal contamination. Producers aiming for high-purity output often combine advanced filtration with inert atmosphere processing. Facilities chasing specific particle shapes or surface areas experiment with hydrothermal synthesis, where pressure and temperature can coax particles to grow a certain way, giving materials tailored for battery, catalyst, or sensor use.
Despite its sturdy face, cupric sulfide has its reactive side. Strong acids like nitric or hydrochloric dissolve it with the evolution of sulfur dioxide or hydrogen sulfide gases, breaking apart the copper-sulfur lattice into soluble ionic forms. Oxidizers like air or hydrogen peroxide convert CuS to copper sulfate and elemental sulfur at higher temperatures, which industrial operations use for recycling or waste management. Laboratory chemists have loaded extra metals or nonmetals onto cupric sulfide backbones, chasing new catalytic behaviors or altered electronic properties. These modifications stretch the potential of the compound, in both fundamental and applied studies, making it much more than just another black powder on a shelf.
Cupric sulfide goes by many monikers, but most revolve around its copper content or its mineral cousin. Covellite represents the naturally occurring form, while copper(II) sulfide appears in technical literature. Some older research calls it cuprate monosulfide, which might pop up in international procurement or niche catalogs. Knowing the right name avoids double-purchasing or confusion in multinational labs, and suppliers print both CAS numbers and synonyms on product documents to cover all bases. In cross-border commerce, translating these names still causes the odd hiccup, but industry experts lean on these established identifiers.
Handling cupric sulfide brings a typical set of lab hazards, especially due to the potential release of hydrogen sulfide gas if the compound meets acids or strong heat. Anyone who’s spent time in a chemistry lab knows to respect those rotten-egg fumes. Organizations teach best practices by maintaining good ventilation and strict personal protective equipment rules. Official safety sheets detail first-aid, spill control, and storage needs, so even novice operators pick up safe habits right from the start. Waste handling regulations require that spent or contaminated cupric sulfide be collected separately from general refuse—nobody wants accidental exposure to copper salts or sulfur gases at a landfill. On the industrial side, permitted exposure levels and workplace monitoring keep the compound from turning into a health risk.
Cupric sulfide finds value far beyond the laboratory. Electronics manufacturers load it into thin-film solar cells and semiconducting layers because it can efficiently shuttle electrons without breaking down. Pigment producers blend it for deep, stable velvet-black colors in ceramics, glass, and architectural materials. There’s traction in battery research too—CuS stands as a promising cathode candidate owing to its robust cycling stability and relatively high theoretical capacity. Mining operations grapple with cupric sulfide during beneficiation of copper ores, owing to its presence in certain mineral deposits. This broad application shows that even a simple binary compound keeps proving useful as industries evolve and technical challenges arise.
Researchers push the limits of cupric sulfide’s use cases. Over the past decade, teams have hacked at the compound’s crystal structure, engineering it for better catalytic conversion in hydrogen evolution or pollutant degradation. Nanostructured forms—think particles a thousandth the width of a hair—reveal extra electrical, magnetic, and surface behaviors, sparking interest in quantum devices and biomaterial synthesis. Analytical chemists run CuS through spectroscopic studies to unlock the subtle links between lattice distortions and physical properties. Drawing from years of experience with transition metal sulfides, I’ve seen cupric sulfide shift from textbook curiosity to trending research topic, highlighting how persistent investigation can revive even long-known materials.
Cupric sulfide sits among those materials that demand real caution, especially in inhalation or ingestion cases. Toxicity studies point to the copper ion as the main culprit—organisms struggle to handle excess copper, leading to organ stress or outright toxicity at high doses. Recent animal studies measure both acute and chronic effects, revealing that exposure over a longer period can disrupt enzyme systems and damage cell membranes. Environmental scientists warn about the risk of copper leaching from contaminated soils or industrial run-off, with downstream effects on aquatic life. Clinical incidents from improper handling offer a stark reminder to treat even familiar substances with respect—training, monitoring, and environmental controls take center stage.
Looking ahead, cupric sulfide stands ready to be shaped by new technologies. Its role in next-generation batteries calls for deeper study into charge–discharge reaction mechanics and real-world cycling stability. Solar cell manufacturers look for ways to combine CuS with other semiconductors, aiming for improved light capture and durable devices. Environmental engineers test its ability as a catalyst in pollution control applications, betting that well-tuned cupric sulfide surfaces could capture or break down hazardous compounds cheaply and efficiently. Across all fields, more sustainable synthesis and safe disposal methods climb the research agenda, pushing manufacturers to rethink every step from mining and delivery through to recycling or reclamation. My experience tells me these transitions won’t be instant or simple, but diligent science and attention to real-world needs keep cupric sulfide grounded in practical progress rather than hype.
Cupric sulfide, known in labs as copper(II) sulfide, brings together copper and sulfur in a dark blue-black solid. It stands out in the mineral world as a naturally occurring substance, but most folks meet it only in classrooms, labs, or factories. You won’t see it hanging out in your kitchen or backyard. In the wild, you might spot it as the mineral covellite, but even then, it keeps to itself in underground veins. The formula is simple: CuS. The story behind cupric sulfide, though, gets much more interesting once you look past the textbook definition.
Chemistry stack shelves with a lot of weird materials, but cupric sulfide stays relevant. Industries depend on its ability to move electrons easily. For anyone curious why old wires rust or why battery research never goes out of fashion, the answer often circles back to how metals like copper pair with elements like sulfur. Cupric sulfide has a knack for helping scientists figure out electrical conductivity and semi-conductive behavior. People use it to dig deeper into how compounds conduct electricity, making it useful for early-stage research in electronics.
Batteries and solar cells lean on compounds like cupric sulfide. Energy-hungry gadgets and green energy panels need materials that let electrons flow in neat, predictable ways. Research into next-generation batteries sometimes looks toward cupric sulfide as a replacement for more expensive or harder-to-find metals. Its use in thin film solar cells shows up in scientific journals and new technology prototypes. Anyone working on finding a cheaper or more stable way to make solar panels pays attention to materials like this.
The pigments industry has roots decades deep in copper chemistry, though cupric sulfide hasn’t had the glamour of other colors. Still, its capacity to add unique shades to certain products—like glass, ceramics, or even plastics—means artists and manufacturers keep it in their toolkit. Of course, they need to handle it carefully, since copper compounds can be toxic if they end up where they shouldn’t.
No chemical comes free from baggage, and cupric sulfide underscores that reality. Left unchecked in waste streams, copper compounds can harm water sources and the organisms living there. I’ve watched communities scramble to tidy up after a spill because even small traces can cause big headaches for fish, plants, and anyone drinking from the river. Factories with good environmental controls stand a better chance of keeping copper compounds contained, but older sites still battle legacy pollution. Workers in facilities using cupric sulfide wear personal protective equipment for a reason.
Experience shows that paying attention early—training workers, updating equipment, and planning for accidents—protects both people and nature. Many researchers work to create safer alternatives or processes that don’t produce as much waste. Some companies invest in recycling techniques that recover copper before it slips into the environment. For regular folks, awareness is the best tool. Demand for cleaner manufacturing, responsible disposal, and thoughtful science keeps chemistry moving in the right direction.
Cupric sulfide often stays backstage, but its role shapes how tech moves forward. From energy storage to artistic ventures, the choices we make in how we use and manage such compounds don’t just influence industry—they ripple through ecosystems and daily life. Step-by-step care, research, and commitment to safety make all the difference.
People in labs might recognize cupric sulfide (CuS) by its inclusion in chemical kits or mineral samples. It shows up as a black, somewhat shiny solid. Try crushing it and you’ll see it keeps its dark color—chemistry hobbyists might compare it to a smear of graphite, just darker. Its density, sitting around 4.6 grams per cubic centimeter, means it packs more heft than common dirt or sand. Despite its solid look, it doesn’t carry any smell or special texture, so you’d barely notice anything strange except for the deep black color.
Cupric sulfide remains stable at room temperature. Toss it in a cup of water and none dissolves, unlike table salt or sugar. It also shrugs off a bath in ethanol. Heating does something more interesting: reach for temperatures above 400°C, and it begins to change in the presence of oxygen, forming copper(II) oxide and releasing sulfur dioxide. Keeping it out of oxidizing atmospheres during high-heat work is crucial if you need the original compound.
The real action with cupric sulfide comes from how copper and sulfur share electrons. The copper holds a +2 oxidation state, which makes this material react quite differently from copper found in coins or pipes. Test its reactivity and sulfur’s double negative charge binds strongly with the copper. Coming into contact with strong acids that release hydrogen ions—like hot hydrochloric or nitric acid—can force the sulfur away, forming hydrogen sulfide gas. This gas stinks like rotten eggs and will catch the attention of anyone nearby, so good ventilation becomes essential in a proper lab.
Although not flammable, cupric sulfide can become hazardous if heated with oxidizers or strong acids. Sulfur-containing compounds like this feed certain bacteria or even provide nutrients for specific plants in the environment, though you’d rarely spot cupric sulfide outside specialized mining or chemistry fields.
Most folks never hear about cupric sulfide outside a classroom or an industrial workflow. A handful of sectors use it as a raw material to make pigments for ceramics or glass, helping glazes reach deep blue or green shades. Electronic materials researchers often put CuS on their radar because its ability to conduct electricity sets it apart. Some solar cell designs lean on thin films containing CuS to catch light and move electrons with more efficiency.
In mining and metallurgy, CuS crops up as covellite, a blue mineral. This mineral gets processed to isolate copper—a metal with real-world value in wiring, plumbing, and machinery. Rarely would anyone try to gather pure CuS on its own in nature without processing other ore.
Cupric sulfide shouldn’t be handled without care. Inhaling dust or getting fine powder in your eyes can cause irritation. Making hydrogen sulfide gas also poses a health risk. Anyone working with this needs access to good protective gear and must rely on proper hoods or fume extractors. Chemical safety organizations point out these hazards, and labs must keep up with regulations to prevent dangerous exposure.
The story of cupric sulfide often circles back to its chemistry. Understanding the link between its dark color, reactivity, and conductivity pushes science forward in small but meaningful ways, from pigments in art to parts in solar panels. Scientists who leverage these properties, without risking health or safety, keep this lesser-known compound firmly in the world of practical chemistry, not just textbooks.
Crammed into certain batteries, pigments, and even as a catalyst in research labs, cupric sulfide (CuS) carries a copper ion paired with sulfur. It’s no newcomer to science, but most folks never see it outside a laboratory container or an industrial process. This black or dark gray powder doesn't make flashy headlines on its own, yet the health and environmental questions around it deserve some daylight.
Breathing in chemical dust is never a smart idea. Copper compounds like cupric sulfide belong on that list. Without a good mask or a working ventilation system, inhaling particles exposes lungs and airways to copper’s rough side. Workers handling cupric sulfide daily risk respiratory problems, headaches, and nausea, especially if they skip wearing proper safety gear. Ingesting or swallowing the substance ramps up risks, and contacting skin or eyes leaves room for irritation or burns.
Longer exposure doesn’t just add up—copper can stick around in the liver and kidneys. Chronic exposure links to weakness, anemia, and, in rare cases, liver failure. The real harm comes when folks treat cupric sulfide carelessly for years, thinking risks only belong to harsher-sounding chemicals.
Scientists track what happens once copper-based chemicals touch soil or water. Cupric sulfide itself isn’t super soluble, but wind or rain breaks it down over time. Copper starts leaching into groundwater or washing into streams. Even small copper increases cause headaches for aquatic life—think fish, snails, and amphibians. Enough copper blocks gill function and pushes out the critters at the bottom of the food chain.
Farmers near dump sites with copper-based waste sometimes notice stunted crops or yellowed leaves. Certain copper levels can poison plants and shut down essential soil bacteria. Nature doesn’t bounce back easily once heavy metals sink in.
Here’s the thing—a lot of facilities that use or store cupric sulfide do follow occupational guidelines, but accidents and shortcuts happen. Some countries enforce strict control on disposal and air quality; others lag behind. The US Occupational Safety and Health Administration and the European Chemicals Agency both flag copper compounds as hazardous when mishandled, so regulations aren’t just paperwork.
Solutions don’t require new inventions. Good ventilation, sealed containers, and spill kits keep workers safer. Regular soil and water checks near factories or waste sites prevent long-term leaks. Education still matters more than wishful thinking—most accidents shrink once people know what’s at stake.
Research can grow greener ways to recycle copper from chemical waste. Pressure is mounting to swap out copper compounds for safer substitutes, particularly in schools and consumer products. Meanwhile, basic steps like gloves, goggles, and transparent reporting help protect people and the environment today.
Cupric sulfide won’t disappear from industry tomorrow, but ignoring its risks only grows the price tag in health bills and damaged ecosystems. Respect for chemicals and a bit of caution go a long way, especially when facts and human stories guide the way. Every workplace and community deserves the chance to manage these risks before they grow beyond control.
Cupric sulfide stands out as a deep black or brown powder, prized in industry and laboratories for its role in electronics, pigments, and research. At first glance, it looks harmless, but this material deserves respect. Mishandling cupric sulfide can spark unwanted chemical reactions, create messes that linger, and result in harm to those who work with it.
Let’s talk storage. Tossing chemicals onto crowded shelves sets a scene for disaster. Cupric sulfide reacts with strong acids, producing toxic hydrogen sulfide gas. Wet hands or a leaky container only serve to multiply risks. To dodge these problems, keep cupric sulfide in well-sealed, clearly labeled containers. Glass or tightly capped plastic works. Tuck these containers away from acids or anything that could spill or leak. Stainless steel and ceramic workbenches handle the powder best; wooden ones soak up residues and create future headaches.
I learned the importance of isolation in a college lab, watching a spill travel fast through containers crowded together. A separate, ventilated cabinet for compounds with dangerous byproducts keeps air fresh for workers and curbs cross-contamination. Always store the powder in a dry place. Dampness opens the door to slow leaks and caking, and it can cause slow, creeping reactions you don’t want. This may sound basic, but labeling and clear records help more than you think. In shared spaces, workers sometimes grab the wrong thing if a jar’s label fades or smudges, which risks confusion and stray reactions.
Anyone handling cupric sulfide without gloves and goggles is betting with their health. Dust floats easily, and nobody wants fine black particles irritating eyes or lungs. Always wear gloves, fitted goggles, and a dust mask or respirator with a fine filter.
Good ventilation turns a hazardous job into a routine task. Fume hoods or extractors pull dust and fumes away from faces and clothes, so take the time to use them every time, not just for big jobs. Cleaning up after spills requires careful attention. Even a small amount can stain skin or produce lingering smells unless scrubbed up with the right chemicals. Sweep powder gently onto damp cloths or use a vacuum rated for fine powders, not a regular broom or household vacuum that spreads material through the air.
My old supervisor used to store a spill kit right next to high-risk chemicals. Absorbent liners, disposable gloves, and a face shield make cleaning safer and faster. After a cleanup, always check that tools and surfaces show no sign of leftover powder or visible contamination.
Mistakes grow costly and dangerous when people don’t talk or share what works. A simple whiteboard noting which chemicals moved where, or who finished a batch, makes sure the next shift knows what to expect. Training matters. New employees deserve a walk-through—not just a handout. Companies should offer short demonstrations of safe transfer and storage, drills on spill response, and clear written guidance that stays in the lab, not in an old binder nobody reads.
Tossing chemical waste into a sink or dumpster crosses a line. Cupric sulfide waste, mixed with solvents or acids, belongs in sealed hazardous waste containers, ready for professional collection. Local regulations may expect records or require special labeling. Keep up with the latest guidance. Safe storage and handling not only protect workers now; they prevent headaches later, avoiding hefty fines and cleaning bills for employers.
Storing and handling cupric sulfide isn’t complicated, but ignoring the basics leads to trouble. Workers who treat every container and cleanup as important keep themselves—and their colleagues—free from harm.
Cupric sulfide isn’t the name most people throw around at the dinner table, but its reach goes farther than expected. I’ve walked through labs where black powders sit in crowded vials, and most people don’t see beyond the surface—pun intended. Chemically, cupric sulfide means a single copper atom stuck to a sulfur atom, forming a mineral called covellite. Simple stuff, but its impact stretches across science and industry.
Start with electronics. Our gadgets, from cheap toy cars to expensive smartphones, run on layers of materials you never see. Cupric sulfide shows up in thin-film solar cells as a hole conductor. If you’ve handled a circuit board, thin coatings containing cupric sulfide help shuttle electricity from point A to point B, often without much fuss or spotlight. Semiconductor research depends on materials that don’t suck up much energy or break down with time. I’ve seen engineers test one compound after another before circling back to cupric sulfide for its stability and efficiency at low cost.
Chemical plants push the limits every day. For reactions that need a little nudge, cupric sulfide steps in as a catalyst. It keeps chemical reactions moving, especially processes that produce specialty plastics and dyes. For example, producing certain types of industrial dyes—think the colors on athletic wear—depends on cupric sulfide to get the desired shades. In my stint in quality labs, reliable results depended on getting precisely the right batch of this compound.
In energy storage, the world keeps a close eye on anything that could stretch the life of a battery. Cupric sulfide has caught attention recently as an experimental material for lithium batteries. It offers good electrical conductivity and manages to hold up after repeated charges. Research teams race to find battery materials that won’t run out quickly or cost a fortune, and cupric sulfide edges onto the shortlist. If you open up a scientific paper on battery innovation, don’t be surprised to see it in the materials section.
Mining companies bump into cupric sulfide while digging for copper. It shows up in ore and tells geologists something about the earth below. In regions that rely heavily on copper mining—like Chile or parts of the southwestern US—understanding its presence helps avoid heavy metal pollution. Mining runoff can spell environmental disaster if not managed well. Cupric sulfide acts as both a marker and a challenge. A few bad spills, and you see communities racing to clean up backyard streams and prevent copper from leaching into farmland.
It isn’t all smooth sailing. Cupric sulfide’s benefits clash with risks. Inhaled dust from processing plants poisons lungs, and long-term exposure can upset ecosystems. It reminds me a bit of cleaning up the garage: ignore the hazards, and things pile up fast. Solutions lie in stricter safety protocols, air filters, and community outreach. No one wants a cheap battery at the cost of ruined health or poisoned soil. Companies following the latest environmental rules, transparent supply chains, and worker training have turned things around for the better in recent years.
If future industries take cues from both science and community needs, cupric sulfide could underpin safer, smarter technologies. More research and open dialogue push us closer to affordable innovations without the leftover scars. From lab tables to electronics factories and mining towns, cupric sulfide leaves its mark—sometimes for better, sometimes for worse.


| Names | |
| Preferred IUPAC name | Copper(II) sulfide |
| Other names |
Copper(II) sulfide
Copper sulfide Cuprous sulfide (incorrectly) Copper monosulfide |
| Pronunciation | /ˈkjuːprɪk ˈsʌlfaɪd/ |
| Identifiers | |
| CAS Number | 1317-40-4 |
| Beilstein Reference | 1206956 |
| ChEBI | CHEBI:77429 |
| ChEMBL | CHEMBL3315489 |
| ChemSpider | 20441311 |
| DrugBank | DB14541 |
| ECHA InfoCard | ECHA InfoCard: 100.029.789 |
| EC Number | 206-934-1 |
| Gmelin Reference | CUPRISULFIDE, Gmelin Reference: "Gmelin 75 |
| KEGG | C18687 |
| MeSH | D003555 |
| PubChem CID | 14831 |
| RTECS number | GL7490000 |
| UNII | 6K384N0P6D |
| UN number | UN3077 |
| CompTox Dashboard (EPA) | `DTXSID7032552` |
| Properties | |
| Chemical formula | CuS |
| Molar mass | 159.16 g/mol |
| Appearance | Black solid |
| Odor | odorless |
| Density | 4.76 g/cm³ |
| Solubility in water | Insoluble |
| log P | -36.67 |
| Vapor pressure | Negligible |
| Basicity (pKb) | 6.7 |
| Magnetic susceptibility (χ) | +53.0·10⁻⁶ cm³/mol |
| Refractive index (nD) | 1.750 |
| Dipole moment | 0 D |
| Thermochemistry | |
| Std molar entropy (S⦵298) | 91.5 J·mol⁻¹·K⁻¹ |
| Std enthalpy of formation (ΔfH⦵298) | -53.6 kJ/mol |
| Std enthalpy of combustion (ΔcH⦵298) | -147.7 kJ/mol |
| Hazards | |
| Main hazards | May cause irritation to the skin, eyes, and respiratory tract. Harmful if swallowed or inhaled. |
| GHS labelling | GHS07, GHS09 |
| Pictograms | GHS07 |
| Signal word | Warning |
| Hazard statements | H410: Very toxic to aquatic life with long lasting effects. |
| Precautionary statements | Wash thoroughly after handling. Do not eat, drink or smoke when using this product. |
| NFPA 704 (fire diamond) | 1-1-0 |
| Lethal dose or concentration | LD50 oral rat: >2000 mg/kg |
| LD50 (median dose) | LD50 (median dose): Oral rat >2000 mg/kg |
| NIOSH | WS5600000 |
| PEL (Permissible) | PEL (Permissible Exposure Limit) for Cupric Sulfide: 1 mg/m³ (as Cu, OSHA) |
| REL (Recommended) | REL (Recommended Exposure Limit): 1 mg/m³ (as Cu) |
| Related compounds | |
| Related compounds |
Copper(I) sulfide
Copper(II) oxide Copper(II) sulfate |