What is the MSDS number for acetone?
CAS# | Chemical Name | EINECS/ELINCS |
---|---|---|
67-64-1 | Acetone | 200-662-2 |
Is acetone toxic MSDS?
Harmful if swallowed. May enter lungs if swallowed or vomited. Prolonged or repeated skin contact may cause drying, cracking, or irritation. High vapor concentrations may cause drowsiness and irritation of the eyes or respiratory tract.
What class is acetone in?
Ketone
Acetone/Classification
What type of hazardous material is acetone?
While it is a widely used product, and is even made in our bodies, acetone is considered a hazardous waste material and needs to be handled and disposed of properly. The potential negative health effects are skin, eye and lung irritation.
At what concentration is acetone hazardous?
Irritant effects have been reported at concentrations of 500 ppm (1210 mg/m3) and higher. Transient effects were reported in workers exposed to 600-2150 ppm (1452-5203 mg/m) (EPA, 1995). Extremely high concentrations (> 29 g/m3) can cause dizziness, confusion, unsteadiness, and unconsciousness (ATSDR, 1994).
What is the flammability rating for acetone?
2 3
NFPA 704 RATINGS FOR COMMON CHEMICALS | ||
---|---|---|
Chemical | Health | Fire |
Acetic acid (glacial) | 2 | 2 |
Acetic anhydride | 2 | 2 |
Acetone | 2 | 3 |
Can acetone fumes harm?
Breathing moderate to high amounts of acetone for a short amount of time can irritate your nose, throat, lungs and eyes. It can also cause headaches, dizziness, confusion, a faster pulse, nausea, vomiting, effects on the blood, passing out and possible coma, and a shorter menstrual cycle in women.
How much acetone is toxic?
A dose of 50 mL (40 g) or more may produce toxic effects (Verschueren, 1983). The minimum lethal dose for a 150-lb man is estimated to be 100 mL (80 g) (Arena and Drew, 1986).
What are the safety hazards of acetone?
What are the potential health effects of acetone?
- Inhalation: Can irritate the nose and throat.
- Skin Contact: May cause mild irritation.
- Eye Contact: EYE IRRITANT.
- Ingestion: Not harmful.
- Effects of Long-Term (Chronic) Exposure: Can cause dry, red, cracked skin (dermatitis) following skin contact.
Is acetone toxic when dry?
The vapour also irritates the eyes. Ingestion: Not harmful. If large amounts are ingested: Can cause effects as described for inhalation. Effects of Long-Term (Chronic) Exposure: Can cause dry, red, cracked skin (dermatitis) following skin contact.
Is 1% acetone flammable?
Pure acetone is a colorless liquid, which has a distinctively sweet, pungent odor. The flashpoint of 0°F (-18°C) makes it a highly flammable liquid, which can ignite even as a low concentration mixture with water.
Is acetone a Class 1 flammable liquid?
Class IA liquids are liquids that have flash points below 73 °F (22.8 °C) and boiling points below 100 °F (37.8 °C). Additionally, unstable flammable liquids are treated as Class IA liquids. Typical Class IB liquids include acetone, benzene, ethyl alcohol, gasoline, and isopropyl alcohol.
What is the molecular formula for dichlorine monoxide?
Dichlorine monoxide. Not to be confused with chlorine monoxide. Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).?) Dichlorine monoxide is an inorganic compound with the molecular formula Cl 2 O.
What is the minimum explosive level for dichlorine monoxide?
Dichlorine monoxide is explosive, although there is a lack of modern research into this behaviour. Room temperature mixtures with oxygen could not be detonated by an electric spark until they contained at least 23.5% Cl 2 O which is an exceedingly high minimum explosive limit.
Why is dichlorine monoxide used as a chlorinating agent?
Dichlorine monoxide is an effective chlorinating agent. It can be used for either the side-chain or ring chlorination of deactivated aromatic substrates. For activated aromatics such as phenols and aryl-ethers it primarily reacts to give ring halogenated products.
Who was the first person to make dichlorine monoxide?
Dichlorine monoxide is an inorganic compound with the molecular formula Cl 2 O. It was first synthesised in 1834 by Antoine Jérôme Balard, who along with Gay-Lussac also determined its composition.