Chemistry isn’t short of curious compounds, but diphenyldichlorosilane stands out for anyone who’s spent time in a synthesis lab. Born in the legacy days of organosilicon chemistry, this molecule landed on the radar not much later than silicon chemistry itself did. Early researchers searching for new ways to bridge organic groups and silicon soon found that chlorosilanes like this one unlocked a toolbox modern chemistry leans on. Before the Second World War, much of the excitement clustered around basic silanes, but soon enough, phenyl substitution pushed the field from hobbyist’s study to foundational industry practice, especially in Europe and the United States. The history doesn’t play out like a Hollywood script — it’s full of trial, error, and the occasional whiff of HCl — but these early ventures set up today’s landscape, where silicon-organic hybrids fuel advances in materials science, coatings, and electronic applications.
Diphenyldichlorosilane comes wrapped up in its own practical story, blending the sturdy backbone of silicon with the organic twist of phenyl rings. Anyone who’s handled it knows both the bite of its chlorine atoms and the bulk its phenyl groups bring. It’s not just a stepping stone compound — in hands looking for versatile starting points, it kicks off all sorts of custom silicon-based chains and structures. Factories don’t churn it out for the fun of it; chemists use it to tailor-make siloxanes, polymers, and tough coatings. For some, its ability to graft phenyl units onto silicon turns out to be the nudge needed for next-generation performance in high-tech applications. Plenty of glassware has been stained and gloves discarded in its name, but few would call it replaceable.
On the bench, diphenyldichlorosilane shows up as a colorless liquid, ready to react with anything holding a trace of water. It doesn’t make a splash with odors, but breathing its fumes triggers an immediate respect for chemical hygiene. The molecule’s weight and boiling point reflect the phenyl group’s heft, and it holds its own in the bottle if kept dry and sealed. Contact with air or moisture brings about the all-too-familiar sight of white fumes and the aroma of hydrochloric acid, proof that not respecting storage advice comes with consequences. Most organic solvents welcome this silane, dissolving it with little fuss, but water remains its quick enemy — a fact every seasoned chemist learns fast. The chemical’s reactivity with nucleophiles, especially alcohols and amines, sets the stage for a grab bag of tailored silicon compounds, and not by accident: practitioners choose it precisely because it hits that rare trifecta of silicon reactivity, hydrophobic bulk, and manageable handling.
The bottle isn’t crowded with marketing slogans. Instead, the typical labels focus squarely on purity, net content, and hazard information. Most reputable suppliers peg content at high purity, often 98 percent or higher, with moisture content kept tightly controlled. Hydrolysis releases hydrochloric acid, which is highlighted on every label worth its job. Labeling conventions reflect a century of regulatory whittling — hazard diamonds, signal words, and precaution statements all do their part to keep handlers alert. There’s no mystique to it, just a focus on safety and a nod to the realities of working with reactive chlorosilanes in a world that expects professionalism and reliability from chemical producers.
Industrial synthesis of diphenyldichlorosilane taps into the weighty tools of Friedel–Crafts chemistry, pairing benzene and silicon tetrachloride with the help of a Lewis acid like aluminum chloride. In labs, people follow the route that history has refined: careful addition, controlled temperatures, and keeping an eye on the evolving mixture. The process produces side products, and separating these out is an art as much as a science, often demanding vacuum distillation. For those who respect the craft, it’s a reminder that organic synthesis still dances between brute force and finesse. Handling the evolving hydrochloric acid isn’t for the faint-hearted, and keeping everything bone-dry is the difference between a clean yield and a polymerized mess.
This silicon compound shows off in the lab. Expose it to water or alcohols, and it hydrolyzes with a rush, leaving hydrochloric acid and silanols or siloxanes behind. Its dichloro groups offer a point of attack for anyone needing to toss on new organic or inorganic moieties. Chemists develop new materials by controlling these reactions, carefully adjusting conditions to get either small molecules or tough network polymers. In the world of advanced polymers, you’ll see it at the starting line for phenyl-rich silicones, especially where thermal stability and weather resistance make or break a material’s performance. Reactions with amines, thiols, or alkoxides open doors to custom organosilicon architectures, and nobody’s just following the textbook — every tweak in reaction conditions can launch new research angles or solve old formulation puzzles.
Chemists don’t agree on much, but when it comes to names, the lexicon grows as fast as the chemistry. In catalogs, you’ll find references to dichlorodiphenylsilane, chlorodiphenylsilane, and even DPCS from those who move fast on the keyboard. These names rarely confuse practitioners: the molecule carries its structure on its sleeve, and anyone working with it knows what to expect — a backbone of silicon, a brace of phenyl groups, and two chlorines that keep reactions lively. Synonyms crop up in product catalogs and regulatory paperwork, but the chemistry always circles back to the same core: a key organosilicon intermediate.
Step into any space where it gets handled, and safety rules make themselves known. Splash-proof goggles, gloves that stand up to solvents, and fume hoods all come standard. Breathing even a trace dances with disaster, since hydrochloric acid forms on contact with humid air or tissue. spills draw immediate cleanup, and the disposal gets handled like the potentially hazardous waste it is. Storage drums sit in climate-controlled, labeled cabinets, with separation from acids, alcohols, and water sources. Workplaces rely on proven methods — dry glassware, regular monitoring, and emergency response plans — to keep both products and people safe. Real-world lab experience teaches quick lessons: a distracted handler courts burns or ruined reactions, but diligence keeps things smooth.
Over the past decades, the uses of diphenyldichlorosilane have stacked up, each one reflecting the intersection of practical chemistry with commercial need. In the world of silicones, its phenyl side chains contribute heat resistance, dielectric strength, and weatherability, making it a staple for electronics insulation, specialty coatings, and sealing materials that have to last in tough conditions. High-end glass fibers, optical materials, and even next-generation battery technologies trace their properties back to its involvement. Research outfits never stop tinkering with how this molecule starts more complex chains; its roots have grown into nanoparticle treatments, surface modifiers, and hybrid organic-inorganic materials. Ask researchers in electronics, they’ll tell you how much the move from methyl to phenyl silicon compounds changed what could be built.
Basic research on diphenyldichlorosilane may have peaked years back, but few areas show signs of slowing. Teams zero in on new approaches for functionalizing silicon surfaces for catalysis or biomedical implants, drawn to the balance between organic mimicry and inorganic durability. Advances in controlled hydrolysis and condensation reaction sequences spark new patents in siloxane resins and coatings. Each published study or patent application adds techniques for finer control, higher selectivity, or faster throughput. The molecule sets an open invitation for modifications, and every shift in synthetic strategy offers a chance to snare new markets or answer unresolved questions in compositional design.
Toxicity questions keep regulators and researchers busy. Direct exposure poses risks, especially through inhalation or skin contact, largely due to how quickly the molecule exchanges its chlorines for hydrogens in biological settings, kicking off hydrochloric acid in the process. Some studies flag acute respiratory distress and irritation as primary concerns, especially with repeated or high-level exposures. Animal trials register organ damage at high doses, which explains why personal protective equipment isn’t up for discussion in any setting where it leaves the bottle. Chronic exposure studies push researchers to dig deeper, as long-term effects still call for careful investigation. Data continues to accumulate, shaped by growing regulatory frameworks and the push to minimize workplace and environmental impact.
What sits on the horizon shows no sign of slowing down for diphenyldichlorosilane. Materials scientists look for stronger, lighter, and more adaptable coatings, pushing this molecule to try on new roles in electronics, energy storage, and biomedical devices. Sustainability pressures challenge old production and disposal habits, so the field wrestles with finding greener, less hazardous methods for synthesis or end-of-life management. As emerging tech fields in nanostructured materials, flexible electronics, and smart coatings catch fire, this compound’s knack for bridging organic and inorganic chemistry ensures it keeps a front-row seat. There’s no sidestepping health and safety, but with research grinding forward, new derivatives and safer handling protocols shape the next chapter for both industry and laboratory. The story of diphenyldichlorosilane reflects a broader truth: chemistry grows by building on the tough, unglamorous foundation stones set by earlier generations, refining them until the next discovery electrifies the field.
Diphenyldichlorosilane doesn’t pop up in most people’s daily conversations. Even so, this organosilicon compound supports quite a bit of what makes manufacturing and materials science tick. Think about all those coatings that protect electronics from dust or moisture, or those sturdy silicone insulators on high-voltage wires. In every case, something has to form that silicon backbone—and this is where diphenyldichlorosilane steps in.
Manufacturers rely on diphenyldichlorosilane as a key starting ingredient for making silicone polymers. These aren’t just plastics with a fancy name. Silicone polymers survive at high temperatures, shake off water easily, and don’t crumble under sunlight. For decades, I’ve seen how silicone rubbers and resins keep everyday tools running longer than they probably should. Medical tubing that bends but never cracks, oven mitts that stay flexible after hundreds of trips through the dishwasher—without strong siloxane links, none of this would look or feel right.
Making those links brings two worlds together: organic chemistry and the utility of inorganic structures. Diphenyldichlorosilane introduces phenyl groups into the silicon chain, and these groups help tailor chemical resistance and mechanical strength. This tweak might sound minor, but for things like gasket seals used in aerospace or automotive settings, it’s the difference between a part that fails after a few months versus something that lasts a whole service cycle.
Electronics have to run in messy conditions. Moisture, oils, and even sneaky chemical vapors can short out microchips or eat away at contacts. Coatings based on silicones offer a kind of armor. Diphenyldichlorosilane lets manufacturers produce these coatings with a tighter molecular network. That means less water seeps through, less swelling, and longer lifespans for circuit boards or sensors. The value really shows up in settings like data centers or factories filled with machinery. Crashes linked to failed insulation cost much more to fix than making reliable coatings from the start.
Organic synthesis sometimes needs a helping hand, especially in the world of pharmaceuticals or high-performance materials. Diphenyldichlorosilane can protect sensitive alcohols and amines during complicated multi-step reactions. By creating a protective silyl group, it shields fragile parts of a molecule from chaos, only to be peeled away at the right time. For chemists, this control over a reaction’s outcome means fewer failed batches and less wasted time. Safety matters too—many other silicon reagents come with higher risks, so using a more manageable compound makes sense for labs trying to balance innovation and responsibility.
With all this potential, diphenyldichlorosilane doesn’t come without its headaches. It reacts sharply with water, releasing hydrochloric acid. The first time I handled it as a trainee, gloves and goggles were just the basics. Facilities need solid ventilation, spill kits, and trained staff to keep things safe. Companies can get ahead of regulatory headaches by sticking to clear protocols, investing in staff education, and designing storage systems to prevent leaks. Switches to closed systems and better detection technology help keep the workplace healthy and the air clean.
Every time a phone charger, medical device, or industrial tool benefits from a bit more durability, there’s a good chance silicone chemistry played a role. The value of diphenyldichlorosilane isn’t in a single flashy use—it’s in the hidden work it puts into products lasting longer, working better, and surviving tough environments.
If you ever get assigned work involving diphenyldichlorosilane, it’s not just another day at the bench. This chemical reacts strongly with water and moist air, shooting out corrosive hydrogen chloride fumes and generating heat that can spark a fire if you’re not careful. I still remember the thick acidic smell that settled in the room the first time someone fumbled with a leaking ampoule. Breathing got rough, eyes started watering, and it took days to scrub away the rust that formed on all exposed metal. That day, most of us walked away with a new respect for good lab routines.
No one plans to get splashed or inhale a cloud of fumes. Yet, more than half the chemical spills I’ve witnessed came down to someone skipping basic gear. Every time diphenyldichlorosilane comes out, I reach for safety goggles—a splash to the eyes can mean permanent injury. Gloves are non-negotiable, but latex won’t cut it. Thick nitrile or butyl gloves prevent burns and stop the chemical from soaking through. Lab coats, chemical splash aprons, and closed shoes form the next line. My friend once trusted old sneakers for a quick transfer; the soles didn’t last five minutes. Lessons like that stick with you.
Containers marked “diphenyldichlorosilane” belong in the fume hood. Good airflow whips away any vapor before it reaches your lungs and irritates your throat. At home, kitchen fans never replace real lab ventilation. Hydrogen chloride forms instantly during transfers and fumes travel fast. Even in a professional setup, I keep the sash low and double-check the exhaust fan. Keeping exposure down can mean the difference between just a whiff and an emergency room visit.
Containers must stay dry and sealed tight. Moisture turns diphenyldichlorosilane into a hazard, corroding lids and glassware. I found out the hard way—one minor leak and every unlined shelf above the container started rusting from condensation. Only open it in dry, controlled environments, away from common acids and alcohols. Cleaning up spills right away with inert absorbents like sand makes a big difference. Never use water for cleaning, since it kicks up a mess of heat and toxic gas. I started double-sealing bottles and double-bagging waste after too many close calls with vapor leaks in the waste bin.
Most accidents happen fast. The best labs I’ve worked in drilled us on emergency eyewash, shower use, and quick spill cleanup. It felt silly at first, walking through what to do if something splashes or leaks. Still, when the real thing happened, muscle memory took over. Reading the latest safety data sheets, practicing evacuation, and making sure fire extinguishers work—these create a safety net for when procedures fail. If you spot a gap or a shortcut, speak up. Nobody should take their first chemical burn as a rite of passage.
Handling diphenyldichlorosilane safely comes down to respect and habit. With growing pressure on labs to cut costs and push throughput, shortcuts look tempting. Yet every moment spent double-checking seals, replacing gloves, or reminding someone to keep the hood sash down, counts toward one simple goal—making sure all of us leave in the same health we came in. Sharing stories, holding regular training, and keeping safety gear up to date fosters a culture where looking out for each other comes naturally. That's how to keep risks in check and prevent serious incidents, no matter how routine the work starts to feel.
Diphenyldichlorosilane sounds like a mouthful, but it sits on the shelves in plenty of labs and manufacturing rooms. Folks use it for high-grade silicone materials and specialty electronics, yet not everyone talks about the real side of storing it safely. I’ve spent a fair bit of time with air-sensitive chemicals, and this one deserves care, not just a spot on a dusty shelf.
Diphenyldichlorosilane reacts fast with water—even the humid air in a regular room spells trouble. You’ll see clouds of hydrochloric acid gas rolling off just from a breeze or a damp hand. That gas is not just irritating; it will carve up your breathing passages and make the room a hazard zone. Silly mistakes, like opening the bottle near a sink, invite preventable accidents.
Every bottle should live in a dry, well-ventilated cupboard, far away from any place where water hangs around. I’ve learned to keep it in tightly sealed containers made from glass or Teflon because metal and plastic degrade and lead to leaks over time. Bags don’t cut it—real seals keep everyone safe.
Stable temperature means more than just a vague “cool and dry.” A lot of people stash sensitive chemicals in the fridge but forget about condensation. Even a quick cycle of chilling and warming brings trouble. I stick with a spot between 2°C and 8°C, away from vents or heaters. Sudden temperature swings might crack a bottle or cause small leaks, so steady storage goes a long way.
Beyond that, avoid sunlight at all costs. UV breaks down a whole range of chemicals and speeds up unwanted reactions.
Labels tend to get smudged and lost after weeks of handling. Always write the opening date, the chemical's full name, and hazards on fresh tape, not just the original bottle label. Nobody should have to guess what’s inside, especially during an emergency.
From experience, a chemical spill labeled only as “reagent” creates chaos. Clear labeling gives responders fast, life-saving info if a bottle breaks.
Big accidents often happen because of sloppy handoffs or poor communication. After one close call, I started keeping a sign-in sheet for every person who handles the bottle. This way, each hand knows exactly what the other did, from inspecting seals to checking expiry dates.
Refresher safety training for everyone dealing with diphenyldichlorosilane makes a difference, too. One worker’s shortcut can undo a whole team’s hard work. Make time for drills—practice clearing spills, donning protective gear, and finding the right neutralizing agent fast.
Companies should invest in clear SOPs for storage and handling, not just generic ones from thirty years ago. Encourage workers to flag old or cracked bottles, and swap them out before they become problems. Safety showers and eye-wash stations should stay close at hand. If budgets allow, chemical storage cabinets with built-in vapor filters add a layer of protection for everyone.
Nothing beats good habits and accountability. Direct communication and real respect for the risks keep people healthy and labs running smoothly.
Diphenyldichlorosilane isn’t a chemical that makes its way into household conversation, but it stays pretty significant in the world of materials science and industrial chemistry. Its formula is C12H10Cl2Si. That might look like a jumble of letters and numbers, but it’s one of those building-block molecules for more advanced materials. It packs two phenyl groups and two chlorine atoms around a single silicon atom, making it reactive and useful for all sorts of high-end manufacturing processes.
The molecular weight clocks in at about 255.20 g/mol. Knowing this number isn’t just academic—engineers and chemists use it whenever they need to measure out precise amounts or plan chemical reactions. It’s how manufacturers keep their production lines consistent, turn out quality materials, and make sure nothing explosive ends up in a reaction vessel.
My time working with chemistry students has shown me it’s easy to overlook what connects these molecules to things outside a lab. People who use touchscreen devices, drive cars, or rely on medical equipment might not realize it, but substances like diphenyldichlorosilane help build the base materials for many of these products. Take silicone polymers, for example. These aren’t just flexible—they’re stable, handle extreme conditions, and resist the kind of wear that would break down ordinary plastics. Diphenyldichlorosilane acts as a key starting material for these polymers.
Chemical companies depend on its reactivity. The two chlorine atoms make diphenyldichlorosilane a perfect candidate for making custom silanes. Those silanes go on to strengthen rubber, protect circuits from water, and even add a protective touch to paints and coatings. The value here shows up in longer-lasting products and designs that work even in tough environments—a big deal in electronics, aviation, and medicine.
Some people ignore warnings about handling industrial chemicals, but experience—sometimes painful—teaches lessons that stick. Diphenyldichlorosilane reacts with water to make hydrochloric acid and diphenylsilanediol. That release of acid can burn skin and eyes and damage lungs if not managed with proper gear. It’s not paranoia that drives industry to demand proper gloves, goggles, and ventilated workspaces. A single accident can close a plant and endanger whole communities.
OSHA offers clear guidance for using volatile organosilanes: strict containment, quick spill cleanup, regular air-quality checks, and ongoing staff education. These aren’t empty rules. What actually happens when companies skip basic safety? Toxic fumes, ruined investments, and sometimes much worse. People’s health comes first, and the right safety steps protect everyone in and around a facility.
Trust in chemical manufacturing depends on companies staying open about what’s in their products and how they control risk. Some producers now list the exact weight and formula of each ingredient they use. Digital tracking systems help regulators verify what enters and leaves each facility. From my perspective, strong oversight from government agencies and clear communication with nearby communities make a real difference. The old days of secretive factories and mystery ingredients left scars—literally and figuratively.
Real progress comes when research, safety, and public information go hand-in-hand. Where possible, research teams look for safer ways to create similar materials while cutting the risks for workers and the public. Better transparency brings a healthier balance between industry growth and community well-being.
Diphenyldichlorosilane’s value reaches beyond its chemical formula and weight. It touches technology, safety, and social responsibility. In every stage—from delivery to disposal—what we learn about these chemicals shapes safer processes, sturdier products, and more honest industries.
Diphenyldichlorosilane hits the radar in workplaces dealing with complex chemicals, especially those connected to the production of silicone polymers or specialty coatings. Right out of the bottle, this compound brings some serious hazards along for the ride. My time in safety training taught me that chemicals with chlorine in their structure often react fast and sometimes violently, especially with water. Diphenyldichlorosilane doesn’t break that pattern. Just a small leak can set off a cloud of hydrogen chloride gas. Anyone who’s had to evacuate a lab after a chemical spill remembers the stinging pain and the rush to fresh air.
Direct contact with the liquid or its fumes quickly becomes dangerous. The eyes, skin, and lungs take the hardest hit. Skin burns, eye injuries, and severe coughing aren’t rare at all. As soon as this compound touches water—even the moisture in the eyes—acid forms instantly. I’ve seen colleagues with red, blistered patches where a splash landed, needing weeks to heal. Inhaling the fumes often leaves sharp pain in the chest and a cough that sticks around. There aren’t many ways to “get used to” this chemical, because symptoms come on strong and fast.
The real trouble happens where safety gear or planning gets skipped. Chemical burns can be deep and long-lasting. Eyesight might never fully recover from an accidental splash. Once we understand how quickly the damage sets in, the need for consistent use of goggles, face shields, chemical-resistant gloves, and proper ventilation feels less like a chore and more like a clear necessity. I’ve watched teams transform their attitude after a single bad incident from cutting corners to counting every bottle and every glove.
Exposure can also spark a chain reaction in the workplace. Hydrogen chloride fumes spread fast and prompt mass evacuation if the ventilation isn’t dialed in. Your neighboring departments and downstream processes could grind to a halt. Lost time and stacked-up cleanup costs put stress on everyone. For companies with a responsibility to keep workers safe, strict protocols around Diphenyldichlorosilane aren't just for show. They protect health, keep operations running, and avoid fines or worse.
When an accident happens, response time and knowledge matter most. Flushing eyes or skin with running water for at least 15 minutes remains the gold standard. I’ve seen this save a coworker’s vision after a split-second splash. Immediate washing prevents acid from digging deeper. Letting up early or skipping steps can mean permanent damage. It’s worth noting that tap water works, but emergency eyewash stations and showers put within arm’s reach make all the difference. If breathing feels tight or someone starts wheezing after exposure, leave the area and seek fresh air—oxygen supplementation helps when serious respiratory symptoms kick in.
Medical attention always comes next, regardless of how “mild” it looks. Cuts in safety budgets sometimes tempt folks to ride it out, but Diphenyldichlorosilane exposure typically gets worse before it gets better. Emergency teams need clear communication: be ready to explain what was spilled, how much got on the person, and how long before the rinse started.
Hazards like Diphenyldichlorosilane highlight the ongoing need for real-world training, not just sign-offs and checklists. Refresher courses, honest safety talks, and up-to-date safety gear save more than money—they protect lives. No fancy protocol ever replaces a team that knows their chemicals inside and out. In work environments where these hazards lurk, creating a culture that puts health first always pays off. Through firsthand experience, I’ve learned that a bit more vigilance today keeps people out of the ER tomorrow.
| Names | |
| Preferred IUPAC name | Diphenyldichlorosilane |
| Other names |
Dichlorodiphenylsilane Diphenylchlorosilane Chlorophenylsilane NCI-C56398 Silane, dichlorodiphenyl- |
| Pronunciation | /daɪˌfiːnɪlˌdaɪˌklɔːrəˈsɪleɪn/ |
| Identifiers | |
| CAS Number | 80-10-4 |
| Beilstein Reference | 1368737 |
| ChEBI | CHEBI:34994 |
| ChEMBL | CHEMBL157141 |
| ChemSpider | 12615 |
| DrugBank | DB14548 |
| ECHA InfoCard | 100.008.671 |
| EC Number | 203-852-3 |
| Gmelin Reference | 70671 |
| KEGG | C06812 |
| MeSH | D004186 |
| PubChem CID | 66196 |
| RTECS number | VV5950000 |
| UNII | L5W86G367A |
| UN number | UN2062 |
| Properties | |
| Chemical formula | (C6H5)2SiCl2 |
| Molar mass | 233.16 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Odor | Aromatic |
| Density | 1.3 g/mL at 25 °C |
| Solubility in water | Reacts |
| log P | 3.7 |
| Vapor pressure | 0.2 mmHg (20°C) |
| Acidity (pKa) | Acidity (pKa): "9.80 |
| Basicity (pKb) | 11.9 |
| Magnetic susceptibility (χ) | -47.0e-6 cm³/mol |
| Refractive index (nD) | 1.597 |
| Viscosity | 3.12 mPa·s (25 °C) |
| Dipole moment | 1.48 D |
| Thermochemistry | |
| Std molar entropy (S⦵298) | 324.6 J·mol⁻¹·K⁻¹ |
| Std enthalpy of formation (ΔfH⦵298) | -332.6 kJ/mol |
| Std enthalpy of combustion (ΔcH⦵298) | -1170 kJ·mol⁻¹ |
| Pharmacology | |
| ATC code | '' |
| Hazards | |
| GHS labelling | GHS02, GHS05, GHS06, GHS07 |
| Pictograms | GHS05,GHS07 |
| Signal word | Danger |
| Hazard statements | H314: Causes severe skin burns and eye damage. H318: Causes serious eye damage. H335: May cause respiratory irritation. H400: Very toxic to aquatic life. |
| Precautionary statements | P261, P263, P264, P271, P280, P301+P330+P331, P303+P361+P353, P304+P340, P305+P351+P338, P312, P321, P330, P363, P405, P501 |
| NFPA 704 (fire diamond) | 3-2-1-W |
| Flash point | > 85 °C (185 °F) |
| Autoignition temperature | Autoignition temperature: 500°C |
| Lethal dose or concentration | LD50 oral rat 2350 mg/kg |
| LD50 (median dose) | 235 mg/kg (rat, oral) |
| NIOSH | WZ5250000 |
| PEL (Permissible) | PEL (Permissible Exposure Limit) of Diphenyldichlorosilane: "1 ppm (5 mg/m³) (OSHA) |
| REL (Recommended) | 3 ppm |
| IDLH (Immediate danger) | 50 ppm |
| Related compounds | |
| Related compounds |
Diphenylsilane Diphenyldimethoxysilane Triphenylchlorosilane Phenyltrichlorosilane |