| Boiling Point | 190°C at 35 mmHg (lit.) |
| Melting Point | 16–19°C (lit.) |
| Density | 1.265 g/mL at 25°C |
| Flash Point | >110°C |
| Color | Yellow |
| Formula Weight | 190.63 |
| Physical Form | Clear Liquid at 20°C |
| Chemical Name or Material | 1-Naphthoyl Chloride |
| UN Number | UN3265 |
| Molecular Formula | C11H7ClO |
| Molecular Weight | 190.63 g/mol |
| SMILES String | ClC(=O)c1cccc2ccccc12 |
| CAS Number | 879-18-5 |
| EC Number | 212-903-9 |
| Recommended Storage Temperature | 2–8°C under inert gas, tightly sealed |
| NACRES | NA.22 |
| UNSPSC Code | 12352100 |
| MDL Number | MFCD00004002 |
| PubChem CID | 70146 |
| Beilstein/REAXYS Number | 775785 |
| InChIKey | NSNPSJGHTQIXDO-UHFFFAOYSA-N |
| Color / Physical Form (Sarchem spec, kept) | Yellow / Clear liquid at 20°C |
| PubChem SID | 24855045 |
1-Naphthoyl chloride is the acid chloride of 1-naphthoic acid — a pale yellow liquid that acylates alcohols and amines to form naphthalene esters and amides. The peri-hydrogen near its carbonyl chloride makes it notably more reactive than simpler aroyl chlorides like benzoyl chloride, which also means it reacts vigorously with atmospheric moisture.
Used to build naphthalene-containing pharmaceutical and agrochemical scaffolds via standard acylation, and to derivatize weakly-detectable analytes (fatty alcohols, mycotoxins) into naphthalene-tagged compounds for HPLC UV/fluorescence detection. Also used in Arndt-Eistert homologation and naphthoyl-indole synthesis.
No related products found.
As an acylating agent for naphthalene esters/amides in pharma/agrochemical synthesis, and as an HPLC derivatization reagent.
Yes — GHS Skin Corrosion Category 1B (Danger, H314); causes severe skin burns and eye damage.
879-18-5, C11H7ClO, MW 190.63 g/mol — do not confuse with 2-Naphthoyl chloride (CAS 2243-83-6).
Sealed, under inert atmosphere, ideally refrigerated 2–8°C, away from moisture.
Yes — hydrolyzes to 1-naphthoic acid and HCl gas; handle under anhydrous conditions.