3-chloropropanoic acid

C3H5ClO2

CAS107-94-8

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Identification

CAS Number
107-94-8
EC Number
203-534-4
UN Number
3261
PubChem CID
7899

Physical-chemical properties

Molecular Formula
C3H5ClO2
Molar Mass
108.52 g/mol
IUPAC Name
3-chloropropanoic acid

Chemical Identifiers

InChI
InChI=1S/C3H5ClO2/c4-2-1-3(5)6/h1-2H2,(H,5,6)
InChI Key
QEYMMOKECZBKAC-UHFFFAOYSA-N

Overview

3-chloropropanoic acid (CAS 107-94-8) is a halogenated carboxylic acid with corrosive properties and versatile synthetic applications. This organochlorine compound, with molecular formula C3H5ClO2, represents an important intermediate in organic synthesis and industrial chemistry. The presence of both a chlorine substituent and a carboxyl functional group makes 3-chloropropanoic acid a valuable building block for various chemical transformations. Its structure features a three-carbon chain with the chlorine atom positioned at the terminal carbon, distinguishing it from other chloropropanoic acid isomers. The compound exhibits typical properties of halogenated carboxylic acids, including moderate solubility in water and polar organic solvents. Its corrosive nature, classified under ADR Class 8, requires appropriate handling protocols and storage conditions. The molecule's reactivity stems from the electron-withdrawing effects of both the chlorine atom and carboxyl group, making it susceptible to nucleophilic substitution reactions and other synthetic transformations. In industrial applications, 3-chloropropanoic acid serves primarily as a chemical intermediate in pharmaceutical synthesis, particularly for producing amino acids and their derivatives. It also finds use in the manufacture of specialty polymers and as a precursor in agrochemical production. Unlike more complex acyl chlorides such as 4-methoxybenzoyl chloride, this compound offers simpler handling characteristics while maintaining high synthetic utility. The compound's versatility extends to research applications, where it serves as a starting material for developing new chemical entities and studying reaction mechanisms involving halogenated carboxylic acids. OYSI provides reliable access to 3-chloropropanoic acid for European industrial customers requiring consistent quality and technical support.

Safety & Classification

No Hazard Classification

This substance is not classified as hazardous according to CLP Regulation (EC) No 1272/2008.

Transport (ADR)

UN Number3261
ADR Class8
Packing GroupII
Tunnel CodeE
Proper Shipping Name3-Chlorpropionsäure, geschmolzen
Marine PollutantNo

Frequently Asked Questions

What is 3-chloropropanoic acid?

3-chloropropanoic acid is an organochlorine compound with the molecular formula C3H5ClO2 and CAS number 107-94-8. This chemical features a three-carbon carboxylic acid chain with a chlorine atom attached to the terminal carbon. With a molecular weight of 108.52 g/mol, it serves as an important intermediate in organic synthesis and pharmaceutical manufacturing, offering unique reactivity due to the presence of both carboxylic acid and chloroalkyl functional groups.

What are the physicochemical properties of 3-chloropropanoic acid?

3-chloropropanoic acid is typically a colorless to pale yellow liquid or crystalline solid at room temperature. It exhibits good solubility in water and polar organic solvents due to its carboxylic acid functionality. The compound has a characteristic acidic odor and demonstrates typical carboxylic acid behavior with a pKa around 4. Its chloroalkyl structure makes it reactive toward nucleophiles, and it can undergo typical esterification, amidation, and substitution reactions.

What is 3-chloropropanoic acid used for?

3-chloropropanoic acid serves as a versatile intermediate in organic synthesis, particularly in pharmaceutical and agrochemical manufacturing. It is commonly used for producing various derivatives through nucleophilic substitution reactions, where the chlorine atom can be replaced with different functional groups. The compound also finds applications in polymer chemistry, as a building block for specialty chemicals, and in research laboratories for synthetic organic chemistry projects requiring halogenated carboxylic acid intermediates.

How to handle 3-chloropropanoic acid safely?

3-chloropropanoic acid should be handled with standard laboratory safety precautions including wearing appropriate personal protective equipment such as chemical-resistant gloves, safety goggles, and lab coats. Work in well-ventilated areas or under fume hoods to avoid inhalation of vapors. Avoid skin and eye contact, and prevent ingestion. Use proper handling techniques to minimize spills and ensure all containers are properly labeled and sealed when not in use.

How to store 3-chloropropanoic acid correctly?

3-chloropropanoic acid should be stored in tightly sealed containers in a cool, dry, well-ventilated area away from direct sunlight and heat sources. Keep containers upright and properly labeled with hazard information. Store away from incompatible materials such as strong bases, oxidizing agents, and reactive metals. Maintain storage temperatures as recommended by the supplier and ensure containers are made of compatible materials that resist corrosion from acidic substances.

What to do in case of contact with 3-chloropropanoic acid?

In case of skin contact with 3-chloropropanoic acid, immediately remove contaminated clothing and rinse the affected area with plenty of water for at least 15 minutes. For eye contact, flush eyes with clean water for at least 15 minutes and seek medical attention. If inhaled, move the person to fresh air and monitor breathing. In case of ingestion, do not induce vomiting and seek immediate medical attention. Always consult safety data sheets for specific first aid measures.

How to dispose of 3-chloropropanoic acid properly?

3-chloropropanoic acid waste must be disposed of according to local, national, and international environmental regulations. Do not pour down drains or release into the environment. Collect waste in appropriate containers and arrange disposal through licensed waste management companies specialized in chemical waste. Consider neutralization procedures where appropriate and permitted. Maintain proper documentation of waste disposal activities and follow your facility's waste management procedures for halogenated organic compounds.

How to transport 3-chloropropanoic acid?

3-chloropropanoic acid is classified under ADR Class 8 (Corrosive substances), Packing Group II, indicating it requires specific transport regulations for corrosive materials. It must be packaged in UN-approved containers suitable for corrosive substances and properly labeled with appropriate hazard markings. Transport documents must include proper shipping names and hazard classifications. Only use transport companies experienced in handling corrosive chemicals and ensure compliance with international dangerous goods regulations.

Is 3-chloropropanoic acid subject to specific regulations?

3-chloropropanoic acid is subject to various chemical regulations including REACH registration requirements in Europe for commercial use above specified tonnage thresholds. It must be classified and labeled according to CLP regulation standards, though it currently shows no specific GHS classifications in available data. Users must comply with occupational safety regulations, environmental protection laws, and transport regulations for corrosive substances. It is not currently listed as a Substance of Very High Concern (SVHC).

Where to buy 3-chloropropanoic acid in Europe?

3-chloropropanoic acid is available through OYSI, a specialized European distributor of technical chemicals. OYSI provides reliable supply of quality chemical products to industrial and research customers across Europe. As an established chemical distributor, OYSI ensures proper documentation, regulatory compliance, and technical support for customers requiring 3-chloropropanoic acid for their applications. Contact OYSI directly for availability, specifications, and pricing information tailored to your specific requirements.

Data Sources

Classification per CLP Regulation (EC) No 1272/2008. Data from ECHA and PubChem.