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HS Code |
643170 |
| Chemicalname | Diphenylaminechloroarsine |
| Casnumber | 494-03-1 |
| Molecularformula | C12H9AsClN |
| Molecularweight | 277.59 g/mol |
| Appearance | Grayish-green crystalline solid |
| Odor | Irritating, acrid |
| Meltingpoint | 111-112 °C |
| Boilingpoint | Decomposes before boiling |
| Solubility | Insoluble in water, soluble in organic solvents |
| Density | 1.44 g/cm3 |
| Vaporpressure | Very low at room temperature |
| Flashpoint | Non-flammable |
| Synonyms | Clark 1, Adamsite |
As an accredited Diphenylaminechloroarsine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Diphenylaminechloroarsine is packaged in a sealed, labeled amber glass bottle containing 100 grams, with hazardous material and handling warnings. |
| Shipping | Diphenylaminechloroarsine should be shipped in tightly sealed containers, clearly labeled as toxic and hazardous. The chemical must be packaged according to international transport regulations for dangerous goods, kept away from heat, moisture, and incompatible substances. Ensure the package is handled by trained personnel, with emergency measures in place during transit. |
| Storage | Diphenylaminechloroarsine should be stored in tightly sealed containers within a cool, dry, well-ventilated, and secure chemical storage facility. Keep it away from sources of heat, ignition, and incompatible substances such as strong oxidizers and strong acids. It must be clearly labeled and handled only by trained personnel using appropriate personal protective equipment to prevent exposure or accidental release, as it is highly toxic. |
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Purity 98%: Diphenylaminechloroarsine purity 98% is used in chemical agent testing, where it ensures accurate assessment of respiratory response. Melting point 130°C: Diphenylaminechloroarsine melting point 130°C is used in laboratory synthesis, where it provides thermal stability during compound formation. Particle size <10 µm: Diphenylaminechloroarsine particle size <10 µm is used in aerosol dispersion studies, where it enables uniform airborne distribution. Stability temperature 25°C: Diphenylaminechloroarsine stability temperature 25°C is used in material storage, where it maintains chemical integrity over time. Molecular weight 282.6 g/mol: Diphenylaminechloroarsine molecular weight 282.6 g/mol is used in toxicological research, where it allows precise calculation of dosage effects. Volatility moderate: Diphenylaminechloroarsine volatility moderate is used in controlled exposure experiments, where it facilitates reproducible vapor generation. |
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In the field of specialty chemicals, few substances bring as much conversation as diphenylaminechloroarsine. This compound draws a line through twentieth-century history, rooted to its specific chemical capabilities. Its structure, C12H9AsClN, sets it apart from other organoarsenic agents. Here in our production facility, we approach this compound with respect for its unique reactivity and distinct industrial context.
We have focused on the careful synthesis and quality management of diphenylaminechloroarsine, following a process that demands reliable handling of reagents, controlled reaction conditions, and rigorous purification to achieve a pure, consistent crystalline material. The resulting product is a white to pale-yellow powder, usually offered at a technical grade with purity above 98%, ticking off the benchmarks valued in historical repositories and contemporary references.
Production of diphenylaminechloroarsine was built up for specific applications, not for general use. Most notably, the compound served as a component in gas mixtures and smoke agents in early-vintage warfare contexts and experimental systems. It’s classified as a vomiting or sternutator agent, triggering intense physiological irritation. This purpose has faded, with international conventions and national regulations placing tight restrictions on its deployment and manufacturing.
Today, the compound’s main audience is scientific. Interest has shifted to detection, analytical chemistry, and legacy research. Researchers and historians alike consult authentic diphenylaminechloroarsine for comparative toxicology studies, instrument calibration, and method validation. Only a handful of firms with deep chemical synthesis experience and historical production background continue to supply this agent for these limited, authorized investigations.
There’s often discussion in technical forums about how difficult it is to make diphenylaminechloroarsine with reliable purity. The process demands access to arsenic trichloride and diphenylamine of known composition. Our team operates in specialized reactors, under inert atmospheres, using temperature modulation and careful agitation to promote desired coupling while minimizing side-products like oxidized arsenic residues or substituted amines.
A common pitfall observed by inexperienced labs comes from inadequate control of moisture and impurities. Water intrusion sparks hydrolysis, generating color bodies that contaminate the product. Purification routines involving repeated recrystallization and filtration filters out much of this risk, though these steps erode yield and inflate cost. These are not challenges that can be solved with generic methodologies; they arise from the stubborn specifics of organoarsenic chemistry.
Our plant invests in dedicated containment areas and advanced filtration to ensure that cross-contamination does not occur when diphenylaminechloroarsine appears anywhere on the schedule. We track each lot from raw input to finished batch with physical inspection, chromatography, and titrimetric confirmation. Deviations in melting point, color, or particle consistency flag a halt for root-cause analysis and remediation. This discipline stems not from regulatory bureaucracy, but from battleground lessons and real-world feedback. The difference in performance — even in small analytical test runs — comes down to these hands-on practices.
Diphenylaminechloroarsine presents as a fine crystalline powder. It has a melting point in the range of 110–114°C. Under standard storage conditions, its physical form remains stable for long periods if shielded from moisture and UV. Many chemicals in adjacent classes show greater volatility or susceptibility to photodecomposition, but this compound maintains integrity if kept in airtight, amber-lined containers away from direct sunlight.
Handling the substance differs dramatically from working with less reactive historic chemicals. In our plant, we use sealed transfer systems, local exhaust ventilation, and purpose-built PPE routines. Any accidental release into the air must be avoided; the substance’s irritating action is pronounced even at low airborne concentrations. Facility safety officers drill all operators on procedures, tool checks, and correct personal decontamination, echoing the principle that every molecule needs to be contained from synthesis to shipment.
Incineration is the best practice for off-spec waste disposal, using high-temperature protocols that convert arsenic compounds to inert, manageable solids under strict environmental controls. Solutions for reducing hazardous waste in batch production involve fractional distillation and arsenic-specific scavengers, tuned and updated by our on-site engineers to address each campaign’s unique output.
People often group diphenylaminechloroarsine with other arsenical and phenylamine derivatives. From our manufacturing vantage point, clear boundaries run between this compound and others, such as diphenylchloroarsine or phenylarsine dichloride. Key differences start at the molecular level: diphenylaminechloroarsine joins two phenyl rings through a nitrogen, which then bonds to arsenic, giving the molecule a greater size and altered electron distribution.
In practice, these differences affect everything from handling hazards to reactivity. For instance, diphenylchloroarsine (DA) lacks the secondary amine linkage, resulting in distinctive byproducts during both synthesis and decomposition. DA vaporizes more easily, bringing slightly greater volatility, but diphenylaminechloroarsine delivers more potent mucous membrane effects. We have documented that for laboratory settings, glassware used for DA is easier to rinse and clear, while the more adherent residue of diphenylaminechloroarsine requires stronger, more targeted cleaning solutions and greater disposal vigilance.
From a chemical durability point of view, both compounds withstand moderate heat and short-term light exposure, though diphenylaminechloroarsine displays a broader safe storage window. No two chemicals from this class respond identically to modern detection techniques, creating both challenge and advantage for analytical chemists interested in differentiating historical samples.
Clients who seek diphenylaminechloroarsine may not always realize that material from different producers varies substantially. We encourage buyers to ask pointed questions about sample provenance, as well as physical and chemical characterization. Independent verification of arsenic content and confirmation of identity by NMR or mass spectrometry gives extra confidence, particularly in small-scale scientific or forensic investigations.
Shipping the compound involves specialized protocols. We use sealed glass ampoules or double-lined polyethylene containers encased in metal drums with secondary containment. All packages include documentation that charts batch synthesis date, test history, and unique barcode. We do not ship to private parties, and require traceable institutional purchase orders for all deliveries.
For projects related to historical agent studies or advanced toxicological modeling, we can support design and execution of pilot-scale syntheses with full transparency about purity and process contaminants. This collaborative approach was born from years of feedback cycles with government agencies and peer-reviewed labs. Resolving tricky questions before shipment prevents disruptions in research, and allows us to serve a broad range of stakeholders with distinct objectives and regulatory constraints.
Manufacturing chemicals with a legacy as complex as diphenylaminechloroarsine requires perspective. The substance embodies hard lessons about scientific progress, unintended consequence, and the moral framework that guides modern chemical practice. International treaties such as the Chemical Weapons Convention draw strict lines around what’s permissible, and we operate within those rules with zero tolerance for deviation.
Our facility audits supply chains, purchases from accredited reagent suppliers, and follows mandatory reporting for sensitive materials. Staff undergo robust compliance training to review not only what the law demands but why these boundaries matter. Rarely does any batch leave the plant without a review by legal and ethical oversight boards, especially if the end user is an institution engaged in academic or forensic investigation.
Internal discussion often circles around the question of legacy. Historical records show that chemical manufacturing, when unchecked, can produce risks that stretch far beyond the factory gate. Our commitment is to transparent, responsible, and strictly limited supply of diphenylaminechloroarsine and related agents, serving only authorized users who can demonstrate a legitimate scientific or regulatory imperative. Any misuse or unauthorized diversion negates every principle that guides our work.
Not all progress comes from big leaps; gradual refinements in technique and facility design make the biggest difference. We have invested in digital controls for process monitoring, which allow for tighter feedback loops and early fault detection in hazardous steps. This reduces human exposure risk — a lesson reinforced by every close call in our decades of plant history.
Breakthroughs in analytical equipment have sharpened our ability to spot impurities earlier. Portable GC-MS and handheld Raman spectrometers give operators near-instant answers, allowing correction before a bad batch proceeds. Over time, these upgrades produce a more stable supply, less waste, and a lower probability of recall. For a compound subject to such close scrutiny, every incremental gain in certainty pays dividends for safety and user confidence.
On the environmental front, we’ve collaborated with chemical engineers and academic partners to pilot advanced waste neutralization and recovery systems tailored for arsenic-rich residues. Success here isn’t measured in line-item savings, but in the cumulative reduction of environmental risk passed on to future generations. Every kilogram of recovered arsenic that doesn’t leave our plant is a win, and a clear expression of value far greater than bottom-line profit.
Manufacturing a chemical like diphenylaminechloroarsine places a plant in the flow of knowledge passing from one era to another. Industrial clients, academic researchers, government experts — each group brings a different angle. Listening to their requirements, their safety questions, and sometimes their anxieties, broadens our awareness of best practice. Some need only gram-scale quantities for method validation, others request larger lots under government contract for historical remediation work. Every inquiry prompts review of storage, handling, and record-keeping protocols to guarantee that end-users find reliability, not hidden risks.
We closely follow published findings and field feedback, adapting process changes if new information points to a better synthesis route or purification method. No amount of textbook theory replaces real-world experience documented by users who perform in-depth testing or forensic analysis. This two-way relationship means each batch not only solves a problem but enriches collective understanding.
We encourage direct conversation, including site visits for major customers or audits by regulatory partners. Seeing the safeguards and workflow in action builds trust that stretches beyond the transaction. The goal extends past selling material—it includes equipping responsible users with insights, actual data, and a sense of shared responsibility for the risks and history carried by this substance.
Diphenylaminechloroarsine stands as a reminder that chemistry knits together material science, safety, ethics, and historical context. We base our manufacturing on daily vigilance, a willingness to embrace change, and dialogue with the scientific and regulatory community. Each lot shipped is more than just a chemical product—it is testimony to evolution in industry standards and shared resolve to prevent past mistakes from repeating. Only by working together with transparency, rigor, and respect for the nuances of compounds like diphenylaminechloroarsine can the goals of science and safety continue to align.