| Boiling Point | 52 °C (lit.) |
| Melting Point | -112 °C (lit.) |
| Vapor Pressure | 11.69 psi (20 °C), 32.33 psi (55 °C) |
| Density | 1.104 g/mL at 25 °C (lit.) |
| Flash Point | 5 °C, closed cup |
| Color | Yellow |
| Linear Formula | CH3COCl |
| Formula Weight | 78.50 g/mol |
| Physical Form | Clear liquid |
| Chemical Name or Material | Acetyl Chloride |
| UN Number | 1717 |
| Molecular Weight | 78.50 g/mol |
| SMILES String | `CC(Cl)=O` |
| Beilstein | 605303 |
| Refractive Index | n20/D 1.389 |
| Explosion Limit | 19% |
| CAS Number | 75-36-5 |
| EC Number | 200-865-6 |
| Key Functional Groups | Acyl chloride |
| NACRES | NA.21 |
| PubChem Substance ID | 329747174 |
| UNSPSC Code | 12352100 |
| MDL Number | MFCD00000719 |
| Quality Segment | 200 |
| InChI | `1S/C2H3ClO/c1-2(3)4/h1H3` |
| InChI Key | WETWJCDKMRHUPV-UHFFFAOYSA-N |
| eCl@ss | 39050501 |
| Autoignition Temperature | 1353 °F |
| Vapor Density | 2.7 (vs. air) |
| Applications | Acetylation reagent in esterification reactions with alcohols to form acetate esters |
Acetyl chloride is the acid chloride of acetic acid, a small, highly reactive molecule in which the hydroxyl group of acetic acid is replaced by a chlorine atom. That substitution makes the carbonyl carbon strongly electrophilic, so the compound reacts rapidly with water, alcohols, and amines — a reactivity profile that makes it useful as an acetylating agent but also means it must be handled under strictly anhydrous conditions. Supplied by Sarchem Labs as a clear liquid with a boiling point of 52 °C and a melting point of −112 °C, it is volatile and flammable, requiring cold, moisture-free, and ignition-source-free storage.
The primary use of acetyl chloride is as an acetylating reagent in organic synthesis: it reacts with alcohols to form acetate esters and participates in Friedel-Crafts acylation reactions to attach acetyl groups directly onto aromatic rings, both fundamental transformations in pharmaceutical and fine-chemical manufacturing. It also serves more specialized analytical and synthetic roles — as a degradation reagent for determining the degree of ethoxylation in polyoxyethylene glycol monoalkyl ethers via chromatography-mass spectrometry, and as a reagent supporting N-Boc deprotection and phosphoramide solvolysis reactions.
Acetyl chloride is both flammable and corrosive and must be handled with full respect for both hazards — this is presented in full below, not softened.
Signal Word: Danger
GHS Pictograms: GHS02 (Flame), GHS05 (Corrosion)
Hazard Classifications: Flammable Liquid Category 2, Skin Corrosion Category 1B, Eye Damage Category 1
Hazard Statements:
Precautionary Statements: P210, P233, P240, P280, P303+P361+P353, P305+P351+P338
Storage Class: 3 — Flammable liquids
Water Hazard Class (WGK): 1
Flash Point: 5 °C, closed cup
Recommended PPE: Face shields, chemical-resistant gloves, and goggles. Handle only in a well-ventilated fume hood, away from all ignition sources and water/moisture, given its violent reaction with water (EUH014).
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Acetyl chloride is used as an acetylating reagent in organic synthesis, most commonly for esterification of alcohols and Friedel-Crafts acylation reactions, as well as in specialized analytical methods and deprotection chemistry.
Yes — acetyl chloride is classified as both highly flammable (H225) and severely corrosive to skin and eyes (H314), and it reacts violently with water (EUH014), so it requires full PPE, anhydrous handling conditions, and a well-ventilated fume hood.
Its electrophilic carbonyl carbon reacts rapidly with water in a hydrolysis reaction that releases hydrochloric acid and heat, which is why it must be stored and handled under strictly moisture-free conditions.
Acetyl chloride is generally more reactive and faster-acting than acetic anhydride, making it useful when a rapid acetylation is needed, though this higher reactivity also means it is more moisture-sensitive and corrosive to handle.
Every order ships with a Certificate of Analysis and Safety Data Sheet, and the product is classified and shipped under UN 1717 in accordance with hazardous-materials transport regulations.