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95054

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Azelaic acid

analytical standard

Synonyme(s) :

Nonanedioic acid

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About This Item

Formule linéaire :
HO2C(CH2)7CO2H
Numéro CAS:
Poids moléculaire :
188.22
Numéro Beilstein :
1101094
Numéro CE :
Numéro MDL:
Code UNSPSC :
85151701
ID de substance PubChem :
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Niveau de qualité

Densité de vapeur

6.5 (vs air)

Pression de vapeur

<1 mmHg ( 20 °C)

Pureté

≥98.5% (GC)

Durée de conservation

limited shelf life, expiry date on the label

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Impuretés

≤0.5% water

Point d'ébullition

286 °C/100 mmHg (lit.)

Pf

106-112 °C
109-111 °C (lit.)

Application(s)

cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care

Format

neat

Chaîne SMILES 

OC(=O)CCCCCCCC(O)=O

InChI

1S/C9H16O4/c10-8(11)6-4-2-1-3-5-7-9(12)13/h1-7H2,(H,10,11)(H,12,13)

Clé InChI

BDJRBEYXGGNYIS-UHFFFAOYSA-N

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Description générale

Azelaic acid (heptane-l,7-dicarboxylic acid), a dicarboxylic saturated acid, is an active component of some topical anti-acne preparations. It is reportedly identified in cosmetics and pharmaceuticals. Azelaic acid is found to suppress the growth of Propionibacterium spp. and reduce keratinization.
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

Azelaic acid may be used as an analytical reference standard for the quantification of the analyte in the following:
  • Tobacco using gas chromatography coupled to mass spectrometry (GC-MS).
  • Topical preparations using reversed-phase liquid chromatographic (LC) with UV-Vis detection.

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Pictogrammes

Exclamation mark

Mention d'avertissement

Warning

Mentions de danger

Classification des risques

Eye Irrit. 2 - Skin Irrit. 2

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

410.0 °F - closed cup

Point d'éclair (°C)

210 °C - closed cup


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Certificats d'analyse (COA)

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Consulter la Bibliothèque de documents

Simultaneous determination of azelaic and benzoic acids in topical preparations by liquid chromatography
Mansour MA and Ibrahiem MM
Chromatographia, 55(7-8), 435-437 (2002)
Simultaneous determination of non?volatile, semi?volatile, and volatile organic acids in tobacco by SIM?Scan mode GC?MS
Wang B, et al.
Journal of Separation Science, 31(4), 721-726 (2008)
Syntheses and QSAR studies of sorbic, cinnamic and ricinoleic acid derivatives as potential antibacterial agents
Narasimhan B, et al.
Indian Journal of Chemistry, 42B, 2828-2834 (2003)
Dongdong Zhang et al.
Oxidative medicine and cellular longevity, 2020, 1295984-1295984 (2021-01-12)
Acute myeloid leukemia (AML) is a hematological malignancy with a poor prognosis attributed to elevated reactive oxygen species (ROS) levels. Thus, agents that inhibit ROS generation in AML should be exploited. Azelaic acid (AZA), a small molecular compound, can scavenge
G Webster
Journal of the American Academy of Dermatology, 43(2 Pt 3), S47-S50 (2000-07-18)
There is no topical antiacne medication that acts against all four of the major pathophysiologic features of acne: hyperkeratinization, sebum production, bacterial proliferation, and inflammation. Topical azelaic acid cream helps both to normalize keratinization and to reduce the proliferation of

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