Skip to Content
Merck
CN

A96150

Azelaic acid

technical grade, 80%

Synonym(s):

1,7-Heptanedicarboxylic acid, Anchoic acid, Nonanedioic acid

Sign In to View Organizational & Contract Pricing.

Select a Size

About This Item

Linear Formula:
HO2C(CH2)7CO2H
CAS Number:
123-99-9
Molecular Weight:
188.22
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24891477
EC Number:
204-669-1
Beilstein/REAXYS Number:
1101094
MDL number:
MFCD00004432
Assay:
80%
Form:
powder

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

form

powder

InChI key

BDJRBEYXGGNYIS-UHFFFAOYSA-N

InChI

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

SMILES string

OC(=O)CCCCCCCC(O)=O

grade

technical grade

vapor density

6.5 (vs air)

vapor pressure

<1 mmHg ( 20 °C)

assay

80%

bp

286 °C/100 mmHg (lit.)

mp

109-111 °C (lit.)

Quality Level

100

Looking for similar products? Visit Product Comparison Guide

Related Categories

General description

Azelaic acid is used as a therapeutic agent in dermatology.

Application

Azelaic acid, a bolaamphiphile, is generally used as a spacer/linker in synthetic chemistry. Some of the applications include:
  • Synthesis of pH-responsive metallo-hydrogels as potential dye-adsorbing agents, and vitamin B12 carriers.
  • Synthesis of fluorescent uranyl (UO22+) coordination polymers.
  • Synthesis of various metal-organic frameworks (MOFs) and supramolecular macrocyclic adducts.
  • Conversion of hydrophobic up-converting rare-earth nanophosphors (UCNPs) into water-soluble, carboxylic acid-functionalized analogs to facilitate conjugation with biomolecules such as streptavidin.

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H315,H319

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

Storage Class

11 - Combustible Solids

wgk

WGK 1

flash_point_f

410.0 °F - closed cup

flash_point_c

210 °C - closed cup

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

新产品
This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
SDBB5421
SDBB2529
STBL3128
STBL0360
STBL2016

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.

Search for a COA

Already Own This Product?

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

Visit the Document Library

Evaluation of the antibacterial efficacy of diesters of azelaic acid.
Charnock C, et al.
European Journal of Pharmaceutical Sciences, 21(5), 589-596 (2004)
Crystal engineering with the uranyl cation I. Aliphatic carboxylate coordination polymers: Synthesis, crystal structures, and fluorescent properties.
Borkowski LA and Cahill CL
Crystal Growth & Design, 6(10), 2241-2247 (2006)
Solid-state preparation of hybrid organometallic-organic macrocyclic adducts with long chain dicarboxylic acids.
Lucaa G, et al.
Chemical Communications (Cambridge, England), 8(37), 3877-3879 (2006)
Pillaring Zn-Triazolate Layers with Flexible Aliphatic Dicarboxylates into Three-Dimensional Metal- Organic Frameworks.
Lin Y-Y, et al.
Crystal Growth & Design, 8(10), 3673-3679 (2008)
pH-responsive, bolaamphiphile-based smart metallo-hydrogels as potential dye-adsorbing agents, water purifier, and vitamin B12 carrier.
Ray S, et al.
Chemistry of Materials, 19(7), 1633-1639 (2007)
View All Related Papers

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