What are the health hazards associated with working with acetylacetone?

Causes respiratory tract irritation. Skin Toxic if absorbed through skin. Causes skin irritation. Eyes Causes eye irritation.

Is acetylacetone polar?

The equilibrium constant tends to be high in nonpolar solvents; the keto form becomes more favorable in polar, hydrogen-bonding solvents, such as water. The enol form is a vinylogous analogue of a carboxylic acid….Tautomerism.

Solvent Kketo→enol
Water 0.23

Where are exposure limits found in MSDS?

Section 8
Section 8: Exposure Controls/Personal Protection This section indicates the exposure limits, engineering controls, and personal protective measures that can be used to minimize worker exposure.

What is acetylacetone used for?

Acetylacetone is used in the production of anti-corrosion agents and its peroxide compounds for the radical initiator application for polymerisation. It is used as a chemical intermediate for drugs (such as sulphamethazine, nicarbazine, vitamin B6, and vitamin K) and pesticides sulfonylurea herbicides and pesticides.

What is the formula of acetylacetone?


Is acetylacetone a liquid?

Acetylacetone is an organic compound with the chemical formula CH3COCH2COCH3. It is a colorless liquid, classified as a 1,3-diketone.

How do I create a safety data sheet?

Steps to writing an SDS

  1. Review OSHA requirements (29 CFR 1910.1200; Guidance for Hazard Determination)
  2. Use OSHA short form or ANSI format.
  3. Review Sigma or other manufacturer’s SDSs for similar products.
  4. Use established Risk and Safety Statements (see Sigma printout).
  5. Include TSCA R&D exemption wording.

How do I find MSDS?

Go on the website of the manufacturer of the product. Once you are on the manufacturer’s website, see if they have a section where they make their MSDSs/SDSs available to the public. You can then search through their MSDSs/SDSs and locate the one for your product.

How do you make acetylacetone?

Acetylacetone has been prepared by the reaction of acetyl chloride with aluminum chloride, followed by hydrolysis;3 by the condensation of acetone with ethyl acetate in the presence of sodium,4 sodium amide,5,6 sodium ethoxide,5,7,8 and alkali or alkaline-earth hydrides;9 by the reaction of acetone and acetic anhydride …