P5561

Propionic acid

Name: Propionic acid
Brand: SIGMA
Price: 215 PLN

BioReagent, suitable for insect cell culture, ~98%

Synonym(s):

Acid C₃, Propanoic acid, Propanyl acid

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1 L

PLN 215.00

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About This Item

Linear Formula:

CH₃CH₂COOH

CAS Number:

79-09-4

Molecular Weight:

74.08

UNSPSC Code:

12352207

NACRES:

NA.71

PubChem Substance ID:

24898668

EC Number:

201-176-3

Beilstein/REAXYS Number:

506071

MDL number:

MFCD00002756

Key Documents

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Product Name

Propionic acid, BioReagent, suitable for insect cell culture, ~98%

SMILES string

CCC(O)=O

InChI

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

InChI key

XBDQKXXYIPTUBI-UHFFFAOYSA-N

vapor density

2.55 (vs air)

vapor pressure

2.4 mmHg ( 20 °C)

product line

BioReagent

assay

~98%

autoignition temp.

955 °F

expl. lim.

12.1 %

technique(s)

cell culture | insect: suitable

refractive index

n20/D 1.386 (lit.)

bp

141 °C (lit.)

mp

−24-−23 °C (lit.)

solubility

H₂O: soluble

density

0.99 g/mL at 25 °C (lit.)
0.993 g/mL at 25 °C (lit.)

Quality Level

100

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Acids

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Show Differences

1 of 4

This Item	402907	94425	P1386
Sigma-Aldrich P5561 Propionic acid	Sigma-Aldrich 402907 Propionic acid	Supelco 94425 Propionic acid	Sigma-Aldrich P1386 Propionic acid
assay ~99%	assay ≥99.5%	assay ≥99.5% (GC)	assay ≥99.5%
Quality Level 100	Quality Level 200	Quality Level 100	Quality Level 200
solubility H₂O: soluble	solubility H₂O: soluble	solubility H₂O: soluble	solubility -
bp 141 °C (lit.)	bp 141 °C (lit.)	bp 141 °C (lit.)	bp 141 °C (lit.)
density 0.99 g/mL at 25 °C (lit.), 0.993 g/mL at 25 °C (lit.)	density 0.993 g/mL at 25 °C (lit.)	density 0.993 g/mL at 25 °C (lit.)	density 0.993 g/mL at 25 °C (lit.)
vapor pressure 2.4 mmHg ( 20 °C)	vapor pressure 2.4 mmHg ( 20 °C)	vapor pressure 2.4 mmHg ( 20 °C)	vapor pressure 2.4 mmHg ( 20 °C)

Application

Use in insect cell culture to inhibit mold growth.

General description

Propionic acid (PA) is a naturally occurring carboxylic acid, which in its pure state exists as a colorless corrosive liquid with an unpleasant odor. It is miscible in water. Industrially it is produced by hydrocarboxylation of ethylene in presence nickel carbonyl as a catalyst.[1] PA has been found to reduce food intake, lower the fatty acids content in plasma and liver, might improve tissue insulin sensitivity and exerts immunosuppressive actions.[2] Propionic acid is an excellent raw material as it is stable, cheap and safe and can even be used as a food additive.[3]

pictograms

GHS02,GHS05,GHS07

signalword

Danger

hcodes

H226,H314,H335

pcodes

P210 - P233 - P240 - P280 - P303 + P361 + P353 - P305 + P351 + P338

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

wgk

WGK 1

flash_point_f

129.2 °F - closed cup

flash_point_c

54 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

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Biological effects of propionic acid in humans; metabolism, potential applications and underlying mechanisms

Sa'ad, H., et al.

Molecular and Cellular Biology, 1801 (11), 1175-1183 (2010)

Nucleophilic ?-Carbon Activation of Propionic Acid as a 3-Carbon Synthon by Carbene Organocatalysis

Jin, Zhichao, et al.

Chemistry?A European Journal , 21 (26), 9360-9363 (2015)

Flour and Breads and their Fortification in Health and Disease Prevention.

Victor R. Preedy, Ronald Ross Watson, Vinood B

Technology & Engineering, 476-476 (2011)

Bindarit, an inhibitor of monocyte chemotactic protein synthesis, protects against bone loss induced by chikungunya virus infection.

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

Drug-metabolizing activity of human and rat liver, lung, kidney and intestine slices.

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

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