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| Product Name | Chlorosulfonyl Isocyanate (CSI) (Synonyms: N-Carbonylsulfamyl Chloride; Sulfuryl Chloride Isocyanate; N-(Oxomethylidene)sulfamoyl Chloride) |
| CAS NO. | 1189-71-5 |
| Formula & Molecular Weight | CClNO3S (Linear Formula: ClSO2NCO) | MW: 141.53 | EC: 214-715-2 |
| Chemical Structure | |
| Product Type | Reactive Synthetic Reagent / LiFSI Precursor / Pharmaceutical Intermediate Chlorosulfonyl Isocyanate contains both chlorosulfonyl and isocyanate groups. This combination makes CSI useful in carbamoylation, sulfonylation, addition, substitution and cyclization reactions. |
| Typical Specification |
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| Reference Properties |
Reference-property values are provided for product identification and process evaluation only. They are not fixed Royalchem batch-release specifications. |
| Key Applications | CSI is a highly reactive bifunctional reagent used in LiFSI precursor production, pharmaceutical carbamoylation and advanced fine-chemical synthesis.
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| Packaging, Storage & Shipping | Packaging: Stainless-steel drums or other compatible special packaging may be provided according to product grade, quantity and dangerous-goods requirements. Final package material and net weight are confirmed with the commercial order. Storage: Keep strictly dry and protect from heat and moisture. Store in tightly closed, compatible containers in a cool, dry and well-ventilated area under suitable inert gas. A storage range of 2–8°C may be used where specified by the applicable supplier TDS or SDS. Shipping: IMDG, IATA and ADR documents commonly classify CSI as UN3265, Class 8, Packing Group II. U.S. DOT documentation may classify it as UN3129, Class 4.3 with subsidiary Class 8, Packing Group II. Final shipping classification is subject to the actual SDS, route, carrier acceptance and destination-country regulations. |
Royalchem supplies Chlorosulfonyl Isocyanate (CSI, CAS 1189-71-5) for bis(chlorosulfonyl)imide and LiFSI precursor routes, cephalosporin carbamoylation and other advanced fine-chemical synthesis applications.
Batch-specific COA, SDS, specification confirmation and route-specific logistics support are available for commercial inquiries. Please provide the target application, assay and impurity requirements, quantity, package requirements and destination country.
| Step 1: HCSI Production | Chlorosulfonyl Isocyanate reacts with chlorosulfonic acid to produce bis(chlorosulfonyl)imide, commonly abbreviated as HCSI. |
| Step 2: Fluorination | HCSI is converted through a suitable fluorination process into bis(fluorosulfonyl)imide, commonly abbreviated as HFSI. |
| Step 3: Lithiation | HFSI is reacted with a suitable lithium-containing compound to produce lithium bis(fluorosulfonyl)imide (LiFSI). |
| Quality Considerations | Purity, moisture and metal-ion control at the CSI and HCSI stages can affect water, free-acid, metal and other critical impurity levels in downstream LiFSI. Customers should provide process-specific quality requirements with the inquiry. |
| Cefuroxime | CSI is used as a carbamoylation reagent in selected cefuroxime routes to construct the carbamoyloxymethyl functionality. |
| Cefoxitin | CSI is used in selected cefoxitin processes for carbamoylation of the corresponding cephalosporin intermediate. |
| Beta-Lactam and Heterocycle Synthesis | CSI can participate in selected addition and cyclization reactions used to construct beta-lactam and other nitrogen-containing ring systems. |
| Sulfonylation and Carbamoylation | Its chlorosulfonyl and isocyanate functionalities make CSI useful for introducing sulfonyl and carbamoyl groups into suitable organic intermediates. |
| What is CAS 1189-71-5? | CAS 1189-71-5 is Chlorosulfonyl Isocyanate, commonly abbreviated as CSI. Its molecular formula is CClNO3S. |
| Does CSI directly produce LiFSI? | Not in a single direct step. CSI is first used to prepare bis(chlorosulfonyl)imide, which is then fluorinated and lithiated through subsequent process stages to produce LiFSI. |
| How is CSI used in cephalosporin synthesis? | CSI acts mainly as a carbamoylation reagent in selected cefuroxime, cefoxitin and related cephalosporin synthesis routes. |
| Why must CSI be protected from moisture? | CSI reacts violently and decomposes on contact with water, potentially releasing corrosive or toxic gases. Storage, sampling and processing must therefore follow the applicable SDS and dry-handling requirements. |
| Why can the CSI shipping classification differ? | Different regulations may classify CSI according to its corrosive or water-reactive hazards. IMDG, IATA and ADR documents commonly use UN3265, while U.S. DOT documentation may use UN3129. The actual batch SDS and route-specific carrier review control the shipment. |
| Can Royalchem provide COA and SDS? | Batch-specific COA, SDS and specification information can be provided. Please include the target application, assay and impurity requirements, quantity, packaging and destination country with the inquiry. |
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