3-Chloropropionic acid Chemical Properties

Melting point:

37 °C

Boiling point:

203-205 °C(lit.)

Density 

1,27 g/cm³

refractive index 

1.4380 (estimate)

Flash point:

>230 °F

storage temp. 

Store below +30°C.

solubility 

H2O: soluble50mg/mL, clear, colorless

pka

3.98(at 25℃)

form 

Crystalline Low Melting Mass

color 

White to beige

PH

<1 (200g/l, H2O, 20℃)

Water Solubility 

freely soluble

Merck 

14,2159

BRN 

1098495

InChIKey

QEYMMOKECZBKAC-UHFFFAOYSA-N

LogP

0.41

CAS DataBase Reference

107-94-8(CAS DataBase Reference)

NIST Chemistry Reference

Propanoic acid, 3-chloro-(107-94-8)

EPA Substance Registry System

3-Chloropropionic acid (107-94-8)

Safety Information

Hazard Codes 

C

Risk Statements 

35-34-21/22

Safety Statements 

26-36/37/39-45

RIDADR 

UN 3261 8/PG 2

WGK Germany 

1

RTECS 

UE8750000

F 

3-10

TSCA 

Yes

HazardClass 

8

PackingGroup 

III

HS Code 

29159080

Hazardous Substances Data

107-94-8(Hazardous Substances Data)

MSDS

• Language:English Provider:3-Chloropropionic acid
• Language:English Provider:SigmaAldrich
• Language:English Provider:ACROS
• Language:English Provider:ALFA

3-Chloropropionic acid Usage And Synthesis

Chemical Properties

white to beige crystalline low melting mass

Uses

3-Chloropropionic acid was used to study the degradation of 3-chloropropionic acid by Pseudomonas sp. strain isolated from rice paddy fields. It was also used in determination of 3-bromopropionic acid, biomarker for the exposure to 1-bromopropane in human urine by gas chromatography

Uses

3-Chloropropionic acid was used to study the degradation of 3-chloropropionic acid by Pseudomonas sp. strain isolated from rice paddy fields. It was also used in determination of 3-bromopropionic acid, biomarker for the exposure to 1-bromopropane in human urine by gas chromatography.

General Description

A white crystalline solid with a sharp odor. Denser than water.

Air & Water Reactions

Water soluble.

Reactivity Profile

2-CHLOROPROPIONIC ACID reacts exothermically with bases. Reacts with aqueous solutions containing a base and dissolves if neutralization generates a soluble salt. May react with active metals to form gaseous hydrogen and a metal salt. May corrode or dissolve iron, steel, and aluminum parts and containers. Reacts with cyanide salts to generate gaseous hydrogen cyanide. Reacts with diazo compounds, dithiocarbamates, isocyanates, mercaptans, nitrides, and sulfides to generate flammable and/or toxic gases and heat. Reacts with sulfites, nitrites, thiosulfates (to give H2S and SO3), dithionites (SO2), to generate flammable and/or toxic gases and heat. Reacts with carbonates and bicarbonates to generate a harmless gas (carbon dioxide) but some heat. Can be oxidized by strong oxidizing agents and reduced by strong reducing agents. These reactions generate heat. A wide variety of products is possible. May initiate polymerization reactions or catalyze other chemical reactions. Fires produces highly toxic chloride fumes [USCG, 1999].

Health Hazard

Contact may cause skin and eye burns. Harmful if swallowed.

Purification Methods

3-Chloropropionic acid [107-94-8] M 108.5, m 41o, 4.08. Crystallise the acid from pet ether or *benzene. [Beilstein 2 IV 748.]

3-Chloropropionic acid(107-94-8)Related Product Information

• Beclomethasone dipropionate
• Ethyl 2-(Chlorosulfonyl)acetate
• Hyaluronic acid
• Stearic acid
• Clobetasol propionate
• Citric acid
• Folic acid
• Ascoric Acid
• 3-Oxo-3-chloropropionic acid methyl ester
• 3-CHLORO-2,2-DIMETHYLPROPIONIC ACID
• 2,3-Dichloropropionic acid
• 3-CHLOROPROPIONIC ACID ETHYL ESTER (BETA) 95+%
• 3-CHLOROBUTYRIC ACID
• Methyl 2,3-dichloropropionate
• CHLOROSUCCINIC ACID
• 2,2-DICHLOROPROPIONIC ACID SODIUM SALT
• Isopropyl 2-chloropropionate
• (S)-(-)-2-Chloropropionic acid