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Azelaic acid

Product Name
Azelaic acid
CAS No.
123-99-9
Chemical Name
Azelaic acid
Synonyms
NONANEDIOIC ACID;Azelex;azelaic;ninandioic acid;ANCHOIC ACID;nonanedioate;Azelaic acid powder;ZK-62498;Azalaic Acid;nonadioic acid
CBNumber
CB6852982
Molecular Formula
C9H16O4
Formula Weight
188.22
MOL File
123-99-9.mol
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Azelaic acid Property

Melting point:
98 °C
Boiling point:
286 °C100 mm Hg(lit.)
Density 
1,029 g/cm3
vapor density 
6.5 (vs air)
vapor pressure 
<1 mm Hg ( 20 °C)
refractive index 
1.4303
Flash point:
215 °C
storage temp. 
Store below +30°C.
solubility 
2.4g/l
form 
Slightly Crystalline Powder or Flakes
pka
4.53, 5.33(at 25℃)
color 
White to slightly yellow
PH
3.5 (1g/l, H2O)
Water Solubility 
2.4 g/L (20 ºC)
Merck 
14,905
BRN 
1101094
Stability:
Stable. Combustible. Incompatible with bases, strong oxidizing agents. Readily biodegrades in soil and water with >70% DOC reduction after 28 days.
InChIKey
BDJRBEYXGGNYIS-UHFFFAOYSA-N
LogP
1.57 at 25℃
CAS DataBase Reference
123-99-9(CAS DataBase Reference)
NIST Chemistry Reference
Nonanedioic acid(123-99-9)
EPA Substance Registry System
Azelaic acid (123-99-9)
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Safety

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
24/25-36-26
WGK Germany 
1
RTECS 
CM1980000
TSCA 
Yes
HS Code 
29171390
Hazardous Substances Data
123-99-9(Hazardous Substances Data)
Toxicity
LD50 orally in Rabbit: > 4000 mg/kg LD50 dermal Rat > 10 g/kg
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

Precautionary statements

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P332+P313IF SKIN irritation occurs: Get medical advice/attention.

P337+P313IF eye irritation persists: Get medical advice/attention.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
8.20117
Product name
Azelaic acid
Purity
for synthesis
Packaging
25g
Price
$65.1
Updated
2024/03/01
Sigma-Aldrich
Product number
8.20117
Product name
Azelaic acid
Purity
for synthesis
Packaging
100g
Price
$131
Updated
2024/03/01
Sigma-Aldrich
Product number
8.20116
Product name
Azelaic acid,
Purity
technical grade for synthesis
Packaging
100g
Price
$45.3
Updated
2024/03/01
Sigma-Aldrich
Product number
8.20116
Product name
Azelaic acid,
Purity
technical grade for synthesis
Packaging
1kg
Price
$112
Updated
2024/03/01
Sigma-Aldrich
Product number
11480
Product name
Azelaic acid
Purity
technical, ~85% (GC)
Packaging
1kg
Price
$134.4
Updated
2024/03/01
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Azelaic acid Chemical Properties,Usage,Production

Description

Azelaic acid is a topical antiacne agent which exerts its therapeutic action through a myriad of antimicrobial, antiproliferative and cytostatic effects. In vitro, azelaic acid hasbeen shown to inhibit DNA polymerases in several tumor cell lines.

Chemical Properties

Azelaic acid is an organic compound with the formula (CH2)7(CO2H)2. This saturated dicarboxylic acid exists as a white powder. It is found in wheat, rye, and barley. It is a component of a number of hair and skin conditioners.

Chemical Properties

white to cream solid

Chemical Properties

Nonanedioic acid is the best known dicarboxylic acid. Its name stems from the action of nitric acid (azote, nitrogen, or azotic, nitric) oxidation of oleic or elaidic acid. It was detected among products of rancid fats. Its origin explains for its presence in poorly preserved samples of linseed oil and in specimens of ointment removed from Egyptian tombs 5000 years old. Azelaic acid was prepared by oxidation of oleic acid with potassium permanganate, but now by oxidative cleavage of oleic acid with chromic acid or by ozonolysis. Azelaic acid is used, as simple esters or branched-chain esters) in the manufacture of plasticizers (for vinyl chloride resins, rubber), lubricants and greases. Azelaic acid is now used in cosmetics (treatment of acne). It displays bacteriostatic and bactericidal properties against a variety of aerobic and anaerobic micro-organisms present on acne-bearing skin. Azelaic acid was identified as a molecule that accumulated at elevated levels in some parts of plants and was shown to be able to enhance the resistance of plants to infections.

Originator

Schering AG (W. Germany)

Uses

antiacne, antiproliferative agent

Uses

antifungal, binds to membrane sterols

Uses

Azelaic acid is used in lacquers, alkyd resins, plasticizers, adhesives, polyamides, urethane elastomers, and organic syntheses. Azelaic acid is also used in treating of acne.

Application

Polymers and related materials
Esters of this dicarboxylic acid find applications in lubrication and plasticizers. With hexamethylenediamine azelaic acid forms Nylon - 6,9, which finds specialized uses as a plastic.
Medical
Azelaic acid is used to treat mild to moderate acne, both comedonal acne and inflammatory acne . It belongs to a class of medication called dicarboxylic acids. It works by killing acne bacteria that infect skin pores. It also decreases the production of keratin, which is a natural substance that promotes the growth of acne bacteria Azelaic acid is also used as a topical gel treatment for rosacea, due to its ability to reduce inflammation . It clears the bumps and swelling caused by Rosacea. Azelaic acid has been used for treatment of skin pigmentation including melasma and post inflammatory hyper pigmentation , particularly in those with darker skin types. It has been recommended as an alternative to hydroquinone (HQ). As a tyrosinase inhibitor, azelaic acid reduces synthesis of melanin.
Brand names
AzClear Action ( 20 % lotion, Ego Pharmaceuticals), Azelex (20% cream, Allergan), White Action cream (20 % cream ,2 % glycolic acid), SynCare), Finacea (15 % gel, Intendis/Berlex Laboratories, subsidiaries of Bayer AG), Finevin (20 % cream, Intendis / Berlex Laboratories), Skinoren (20 % cream or 15% gel, Intendis), Melazepam, Strata Dermatologics, 2oz, Mixed Dicarboxylic Acids 20 % Azelaic Acid Cream.,and Azaclear (azelaic acid and niacinamide, Epikinetics LLC). .

Indications

Azelaic acid (Azelex) is a naturally occurring dicarboxylic acid produced by the yeast Malassezia furfur. Azelaic acid inhibits tyrosinase, a rate-limiting enzyme in the synthesis of the pigment melanin. This may explain why diminution of melanin pigmentation occurs in the skin of some patients with pityriasis versicolor, a disease caused by M. furfur. Azelaic acid is bacteriostatic against a number of species thought to participate in the pathogenesis of acne, including Propionibacterium acnes. The drug may also reduce microcomedo formation by promoting normalization of epidermal keratinocytes.

Production Methods

Azelaic acid is industrially produced by the ozonolysis of oleic acid. The side product is nonanoic acid. It is produced naturally by Malassezia furfur (also known as Pityrosporum ovale), a yeast that lives on normal skin. The bacterial degradation of nonanoic acid gives azelaic acid.

Definition

ChEBI: Nonanedioic acid is an alpha,omega-dicarboxylic acid that is heptane substituted at positions 1 and 7 by carboxy groups. It has a role as an antibacterial agent, an antineoplastic agent, a dermatologic drug and a plant metabolite. It is a dicarboxylic fatty acid and an alpha,omega-dicarboxylic acid. It is a conjugate acid of an azelaate(2-) and an azelaate.

Preparation

Azelaic acid is made by the ozonolysis of oleic acid:

Application

Azelaic acid, also known as azalea acid, is a white to slightly yellow powder. Azelaic acid is a medium-long chain dibasic acid[1]. In recent years, with the rapid development of the organic synthetic chemical industry, the demand for medium and long chain dibasic acids is increasing. The medium and long chain dibasic acids and their derivatives have a wide range of industrial applications and a broad product market.

Manufacturing Process

Two step oxidation of tall oil fatty acid using peroxyformic acid and nitric acid/sodium metavanadate were used to produce azelaic acid.
Step 1 (derivatization of the double bond):
A hydroxy acyloxy derivative of tall oil fatty acid (TOFA) was prepared by mixing 200 g of TOFA (63% oleic acid, 31% linoleic acid) with 500 mL of formic acid. The resulting mixture was vigorously stirred by magnetic action.
Hydrogen peroxide solution, 180 mL of 35% by weight, was added in aliquots to the mixture throughout the course of the reaction. A third of the total amount of peroxide solution was added at once to initiate the reaction. The peroxyformic acid in this case was prepared in situ.
The start of the reaction was signalled by heat evolution and a dramatic color change, from pale yellow to deep rust red. The exothermicity of the reaction required external cooling to control the temperature. The reaction was maintained at 40°C to minimize oxygen loss through the decomposition of the peroxide. As required, the temperature of the reaction was maintained with an external heating source. A total reaction time of 5 to 6 hours was necessary for complete reaction. The end of the reaction was indicated by a color change, the reaction mixture changed from rust red back to yellow. One last aliquot of peroxide solution was added at the end of the reaction period to provide a peroxide atmosphere during the reaction work-up. TOFA as a substrate produced a mixture of mono- and dihydroxy formoxystearic acid from the oleic and linoleic acid components, respectively. The final product was obtained in essentially 100% yield by removing the unreacted formic acid and hydrogen peroxide as well as water. It was obtained as a viscous, syrupy yellow oil that upon gas chromatographic analysis of the methyl esters of the reaction mixture gave no evidence of unreacted substrate.
Step 2 (oxidation of derivative obtained from step 1):
A 2 L three neck flask fitted with an air condenser attached to a gas scrubbing apparatus was filled with 500 mL of concentrated nitric acid (70% by weight). The acid was stirred by magnetic action and 1 g of sodium metavanadate was added to it. The resulting mixture was heated slowly to 40°-50°C. At this point a small amount of product as obtained from Step 1 was added to the acid-catalyst mixture. Heating was continued until a sharp temperature increase accompanied by evolution of NOx gases was observed. The reaction temperature was self-sustained with the addition of aliquots of the hydroxy formoxy ester mixture obtained from Step 1. (External cooling may be required throughout the substrate addition period to keep the temperature within 65°-70°C). At the end of the addition period the reaction temperature was maintained for an additional 1.5 to 2 hours, for a total reaction time of 3 hours.
The final products were obtained by quenching the reaction by adding excess water and extracting the organic layer with purified diethyl ether. The ether extract was dried over anhydrous sodium sulfate overnight before its removal with a roto-vap apparatus. Addition of petroleum ether (boiling range 35°- 60°C) to the product mixture caused precipitation of the diacid component. Vacuum filtration was used to remove the solid diacids from the liquid monoacid mixture. The latter was obtained by removing the excess petroleum ether from the resulting filtrate. Quantitative analysis by gas chromatography of the methyl esters showed that the products to be 96% yield of diacid (66% azelaic, 30% suberic).

brand name

Azelex (Allergan); Finacea (Intendis);Skinoren.

Therapeutic Function

Antiacne, Depigmentor

Synthesis Reference(s)

Journal of the American Chemical Society, 77, p. 4846, 1955 DOI: 10.1021/ja01623a048
Organic Syntheses, Coll. Vol. 2, p. 53, 1943

General Description

Azelaic acid is used as a therapeutic agent in dermatology.

Biochem/physiol Actions

Azelaic acid is a potent inhibitor of 5α-reductase activity. It is a reversible competitive inhibitor of thioredoxin reductase in human melanoma cells.

Mechanism of action

Naturally occurring dicarboxylic acid that is bacteriostatic to Propionibacterium acnes. It also decreases conversion of testosterone to 5{pi}ga-dihydrotestosterone (DHT) and alters keratinization of the microcomedone. It may also be beneficial in the treatment of melasma. The mechanism of action is not fully understood. Deoxyribonucleic acid (DNA) synthesis is reduced, and mitochondrial cellular energy products are inhibited in melanocytes.

Biotechnological Applications

In plants, azelaic acid serves as a "distress flare" involved in defense responses after infection. It serves as a signal that induces the accumulation of salicylic acid, an important component of a plant's defensive response.

Clinical Use

Azelaic acid is used for the treatment of mild to moderate acne, particularly in cases characterized by marked inflammation-associated hyperpigmentation.

Safety Profile

Low toxicity by ingestion. A skinand eye irritant. Closely related to glutaric acid and adipicacid. Combustible when exposed to heat or flame; canreact with oxidizing materials.

Purification Methods

Recrystallise it from H2O(charcoal) or thiophene-free *benzene. The acid can be dried by azeotropic distillation with toluene, the residual toluene solution is then cooled and filtered, and the precipitate is dried in a vacuum oven. It has been purified by zone refining or by sublimation onto a cold finger at 10-3torr. It distils above 360o with partial formation of the anhydride. The dimethyl ester has m –3.9o and b 140o/8mm. [Hill & McEwen Org Synth Coll Vol II 53 1943, Beilstein 2 IV 2055.]

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Azelaic acid Suppliers

Jinan Zhihe Fine Chemical Co., Ltd.
Tel
13854654186
Email
194354110@qq.com
Country
China
ProdList
6
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58
JinanGongchuang Pharmaceutical Technology Co. Ltd..
Tel
0531-88065293 13287783460
Fax
0531-88065293
Email
3166282224@qq.com
Country
China
ProdList
36
Advantage
58
Ningbo Hua Tuo Chemical Co., Ltd.
Tel
+86-0574-88237971 +86-15267895909
Fax
0574-88237323
Email
mia@sinotopchem.com
Country
China
ProdList
60
Advantage
58
Hefei TNJ Chemical Industry Co.,Ltd.
Tel
551-65418679 15837135945
Fax
0551-65418697
Email
info@tnjchem.com
Country
China
ProdList
1889
Advantage
62
Spec-Chem Industry Inc.
Tel
025-84523390 13505162978
Email
sc@specchemind.com
Country
China
ProdList
117
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58
Powerful Chemical (Shanghai) Co., Ltd.
Tel
021-62211590 18917958225
Fax
021-54339019
Email
pwfchem@163.com
Country
China
ProdList
74
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58
Zhengbainian (Shanghai) International Trade Co., Ltd.
Tel
13381511189 13381511189
Email
1514630485@qq.com
Country
China
ProdList
457
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58
Shandong YingLang Chemical Co.,Ltd
Tel
187-66152056 18396883708
Fax
+86-531-88999750
Email
chen@chemwww.com
Country
China
ProdList
4635
Advantage
58
Zhongshan Kexin Biotechnology Co., Ltd
Tel
0760-+86-0760-88665202 13824707890
Email
kexinBiotec@163.com
Country
China
ProdList
138
Advantage
58
J & K SCIENTIFIC LTD.
Tel
010-82848833 400-666-7788
Fax
86-10-82849933
Email
jkinfo@jkchemical.com
Country
China
ProdList
96815
Advantage
76
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View Lastest Price from Azelaic acid manufacturers

WUHAN FORTUNA CHEMICAL CO., LTD
Product
Azelaic acid 123-99-9
Price
US $0.00/Kg/Drum
Min. Order
1KG
Purity
99%min
Supply Ability
1000kgs
Release date
2021-07-13
Hebei Zhuanglai Chemical Trading Co.,Ltd
Product
Azelaic Acid / Ninandioic Acid 123-99-9
Price
US $180.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
20ton
Release date
2024-04-23
Sinoway Industrial co., ltd.
Product
Azelaic Acid 123-99-9
Price
US $0.00-0.00/Kg/Bag
Min. Order
1Kg/Bag
Purity
99% up, High Density
Supply Ability
20 tons
Release date
2024-06-27

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