Skip to Content
Merck
All Photos(1)

Key Documents

81910

Sigma-Aldrich

Propionic acid

puriss. p.a., ≥99.5% (GC)

Synonym(s):

Acid C3, Propanoic acid, Propanyl acid

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
CH3CH2COOH
CAS Number:
Molecular Weight:
74.08
Beilstein:
506071
EC Number:
MDL number:
UNSPSC Code:
12352100
eCl@ss:
39021305
PubChem Substance ID:
NACRES:
NA.21

vapor density

2.55 (vs air)

Quality Level

vapor pressure

2.4 mmHg ( 20 °C)

grade

puriss. p.a.

Assay

≥99.5% (GC)

form

liquid

autoignition temp.

955 °F

expl. lim.

12.1 %

refractive index

n20/D 1.386 (lit.)
n20/D 1.386

bp

141 °C (lit.)

mp

−24-−23 °C (lit.)

solubility

organic solvents: soluble(lit.)
water: soluble(lit.)

density

0.993 g/mL at 25 °C (lit.)

cation traces

Al: ≤0.5 mg/kg
Ba: ≤0.1 mg/kg
Bi: ≤0.1 mg/kg
Ca: ≤0.5 mg/kg
Cd: ≤0.05 mg/kg
Co: ≤0.02 mg/kg
Cr: ≤0.1 mg/kg
Cu: ≤0.02 mg/kg
Fe: ≤0.5 mg/kg
K: ≤0.5 mg/kg
Li: ≤0.1 mg/kg
Mg: ≤0.1 mg/kg
Mn: ≤0.02 mg/kg
Mo: ≤0.1 mg/kg
Na: ≤1 mg/kg
Ni: ≤0.1 mg/kg
Pb: ≤0.1 mg/kg
Sr: ≤0.1 mg/kg
Zn: ≤0.1 mg/kg

functional group

carboxylic acid

SMILES string

CCC(O)=O

InChI

1S/C3H6O2/c1-2-3(4)5/h2H2,1H3,(H,4,5)

InChI key

XBDQKXXYIPTUBI-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

General description

Propionic acid is a linear monocarboxylic acid. It affords esters on reaction with alcohols or alkenes. It can be synthesized by reacting ethane, carbon monoxide and water. It participates as a precursor in the preparation of smallest azolium homoenolate intermediate.

Application

Propionic acid may be used in the synthesis of cellulose propionate (cellulose ester).

Signal Word

Danger

Hazard Statements

Hazard Classifications

Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(F)

129.2 °F - closed cup

Flash Point(C)

54 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Eagleson M.
Concise Encyclopedia Chemistry, 194-194 (1994)
Eagleson M.
Concise Encyclopedia Chemistry, 898-898 (1994)
Zhichao Jin et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 21(26), 9360-9363 (2015-05-28)
Direct β-carbon activation of propionic acid (C2H5CO2H) by carbene organocatalysis has been developed. This activation affords the smallest azolium homoenolate intermediate (without any substituent) as a 3-carbon nucleophile for enantioselective reactions. Propionic acid is an excellent raw material because it
Weiqiang Chen et al.
Journal of virology, 89(1), 581-593 (2014-10-24)
The recent global resurgence of arthritogenic alphaviruses, in particular chikungunya virus (CHIKV), highlights an urgent need for the development of therapeutic intervention strategies. While there has been significant progress in defining the pathophysiology of alphaviral disease, relatively little is known
R De Kanter et al.
Xenobiotica; the fate of foreign compounds in biological systems, 32(5), 349-362 (2002-06-18)
1. Organ-specific biotransformation was studied in human and rat liver, lung, kidney and small intestine slices and compared on a protein basis, using four model substances. 2. Deethylation of lidocaine was highest in liver slices from both man and rat

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service