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| | Metaldehyde Basic information |
| | Metaldehyde Chemical Properties |
| Melting point | 190-196 °C (subl.)(lit.) | | Boiling point | 267.82°C (rough estimate) | | density | 0,808 g/cm3 | | refractive index | 1.4455 (estimate) | | Fp | 50 °C | | storage temp. | 0-6°C | | solubility | Chloroform (Slightly, Heated), Methanol (Very Slightly) | | form | powder | | Water Solubility | 0.2g/L(17 ºC) | | Merck | 14,5923 | | Major Application | agriculture
cleaning products
cosmetics
environmental
food and beverages
personal care | | InChI | 1S/C8H16O4/c1-5-9-6(2)11-8(4)12-7(3)10-5/h5-8H,1-4H3 | | InChIKey | GKKDCARASOJPNG-UHFFFAOYSA-N | | SMILES | CC=O | | LogP | 1.140 (est) | | CAS DataBase Reference | 9002-91-9(CAS DataBase Reference) | | EPA Substance Registry System | Acetaldehyde, homopolymer (9002-91-9) |
| Hazard Codes | Xn,T,F | | Risk Statements | 10-22-23-11 | | Safety Statements | 13-23-46-45 | | RIDADR | UN 1332 4.1/PG 3 | | WGK Germany | 1 | | RTECS | AB3042000 | | TSCA | TSCA listed | | HazardClass | 4.1 | | PackingGroup | III | | HS Code | 29125000 | | Storage Class | 4.1B - Flammable solid hazardous materials | | Hazard Classifications | Acute Tox. 2 Inhalation
Acute Tox. 3 Oral
Flam. Sol. 2 | | Toxicity | Acute oral LD50 for dogs 0.6–1.0 g/kg (Worthing and Hance, 1991). |
| | Metaldehyde Usage And Synthesis |
| Chemical Properties | White crystalline powder | | Uses | META(R) Metaldehyde is a highly effective active ingredient to control slugs and snails (molluscicide) WWW Link | | Uses | In compressed form as a fuel instead of alcohol; molluscicide. | | Definition | A polymer of
acetaldehyde in which n usually is 4–6. | | Definition | A solid compound,C4O4H4(CH3)4, formed by polymerizationof ethanal (acetaldehyde) in diluteacid solutions below 0°C. Thecompound, a tetramer of ethanal, isused in slug pellets and as a fuel forportable stoves. | | Hazard | Flammable, dangerous fire risk. Strong irritant to skin and mucous membranes. | | Carcinogenicity | There is no evidence in the literature
that metaldehyde has carcinogenic potential. | | Environmental Fate | Plant. When applied to citrus rinds, 50% was lost after 4.6 days for the first 33 days
and an additional 25% was lost 14 days for the subsequent 26 days (Iwata et al., 1982).
Chemical/Physical. Metaldehyde can be converted to acetaldehyde by heating to 150°C
for 4–5 hours or by the reaction of concentrated hydrochloric acid (6 M) for a couple of
minutes (Booze and Oehme, 1985). |
| | Metaldehyde Preparation Products And Raw materials |
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