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Octanoic acid

analytical standard

Synonyme(s) :

Acid C8, Caprylic acid

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About This Item

Formule linéaire :
CH3(CH2)6COOH
Numéro CAS:
Poids moléculaire :
144.21
Numéro Beilstein :
1747180
Numéro CE :
Numéro MDL:
Code UNSPSC :
85151701
ID de substance PubChem :
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Niveau de qualité

Densité de vapeur

5 (vs air)

Pression de vapeur

1 mmHg ( 78 °C)

Pureté

≥99.5% (GC)

Durée de conservation

limited shelf life, expiry date on the label

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Indice de réfraction

n20/D 1.428 (lit.)
n20/D 1.428

Point d'ébullition

237 °C (lit.)
237-238 °C

Pf

15-17 °C (lit.)

Densité

0.91 g/mL at 25 °C (lit.)

Application(s)

cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care

Format

neat

Groupe fonctionnel

carboxylic acid

Conditions d'expédition

ambient

Température de stockage

room temp

Chaîne SMILES 

CCCCCCCC(O)=O

InChI

1S/C8H16O2/c1-2-3-4-5-6-7-8(9)10/h2-7H2,1H3,(H,9,10)

Clé InChI

WWZKQHOCKIZLMA-UHFFFAOYSA-N

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Description générale

Octanoic acid is a medium chain saturated fatty acid (MCFA). It is a nutrient present in dairy products and specific oils like palm kernel and coconut oils.
This substance is listed on the positive list of the EU regulation 10/2011 for plastics intended to come into contact with food.

Find all available reference materials for compounds listed in 10/2011 here

Application

Octanoic acid may be used as a reference standard in quantification of the analyte in plasma and brain homogenate by high-performance liquid chromatography with ultraviolet detection.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Produits recommandés

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Pictogrammes

Corrosion

Mention d'avertissement

Danger

Mentions de danger

Classification des risques

Aquatic Chronic 3 - Eye Dam. 1 - Skin Corr. 1C

Code de la classe de stockage

8A - Combustible corrosive hazardous materials

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

>230.0 °F - closed cup

Point d'éclair (°C)

> 110 °C - closed cup

Équipement de protection individuelle

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


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Certificats d'analyse (COA)

Lot/Batch Number

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Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

Revisiting the metabolism and physiological functions of caprylic acid (C8: 0) with special focus on ghrelin octanoylation.
Lemarie F, et al.
Biochimie, 120, 40-48 (2016)
HPLC analysis of brain and plasma for octanoic and decanoic acids.
Dean HG, et al.
Clinical Chemistry, 35(9), 1945-1948 (1989)
Romain Harmancey et al.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 27(10), 3966-3978 (2013-07-05)
Diabetic patients with acute myocardial infarction are more likely to die than nondiabetic patients. In the present study we examined the effect of insulin resistance on myocardial ischemia tolerance. Hearts of rats, rendered insulin resistant by high-sucrose feeding, were subjected
K M Morrill et al.
Journal of dairy science, 95(7), 3987-3996 (2012-06-23)
Our objectives were to evaluate the use of refractometry as a means of estimating immunoglobulin G (IgG) concentration of bovine maternal colostrum (MC) and determine if fractionation of MC using caprylic acid (CA) improved estimates of IgG. Samples (n=85) of
Hong-Fei Tong et al.
Journal of chromatography. A, 1285, 88-96 (2013-03-12)
Hydrophobic charge-induction chromatography (HCIC) is a novel downstream bioprocessing technology for antibody purification and it has several advantages over traditional purification processes. However, its separation selectivity still needs to be improved. In this work, sodium caprylate (NaCA) was used as

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