Welcome to LookChem.com Sign In|Join Free

Cas Database

123-99-9

123-99-9

Identification

  • Product Name:Azelaic acid

  • CAS Number: 123-99-9

  • EINECS:204-669-1

  • Molecular Weight:188.224

  • Molecular Formula: C9H16O4

  • HS Code:2917.19

  • Mol File:123-99-9.mol

Synonyms:1, 9-Nonanedioic acid;Nonanedioic acid;Azelaic acid, technical grade;Lepargylic acid;Heptanedicarboxylic acid;Nonanedioic acid Azelaic acid;Empol 1144;1,7-Heptanedicarboxylic acid;Emerox 1144;Emerox 1110;Ammonium Hydrogen Azelate;Azelaic Acid 99%;

Post Buying Request Now
Entrust LookChem procurement to find high-quality suppliers faster

Safety information and MSDS view more

  • Pictogram(s):IrritantXi

  • Hazard Codes:Xi

  • Signal Word:Warning

  • Hazard Statement:H315 Causes skin irritationH319 Causes serious eye irritation

  • First-aid measures: General adviceConsult a physician. Show this safety data sheet to the doctor in attendance.If inhaled If breathed in, move person into fresh air. If not breathing, give artificial respiration. Consult a physician. In case of skin contact Wash off with soap and plenty of water. Consult a physician. In case of eye contact Rinse thoroughly with plenty of water for at least 15 minutes and consult a physician. If swallowed Never give anything by mouth to an unconscious person. Rinse mouth with water. Consult a physician. /SRP:/ Immediate first aid: Ensure that adequate decontamination has been carried out. If patient is not breathing, start artificial respiration, preferably with a demand valve resuscitator, bag-valve-mask device, or pocket mask, as trained. Perform CPR if necessary. Immediately flush contaminated eyes with gently flowing water. Do not induce vomiting. If vomiting occurs, lean patient forward or place on the left side (head-down position, if possible) to maintain an open airway and prevent aspiration. Keep patient quiet and maintain normal body temperature. Obtain medical attention. /Poisons A and B/

  • Fire-fighting measures: Suitable extinguishing media SMALL FIRE: Use DRY chemical powder. LARGE FIRE: Use water spray, fog or foam. Do not use water jet. Wear self-contained breathing apparatus for firefighting if necessary.

  • Accidental release measures: Use personal protective equipment. Avoid dust formation. Avoid breathing vapours, mist or gas. Ensure adequate ventilation. Evacuate personnel to safe areas. Avoid breathing dust. For personal protection see section 8. Prevent further leakage or spillage if safe to do so. Do not let product enter drains. Discharge into the environment must be avoided. Small spill: Use appropriate tools to put the spilled solid in a convenient waste disposal container. Finish cleaning by spreading water on the contaminated surface and dispose of according to local and regional authority requirements. Large spill: Use a shovel to put the material into a convenient waste disposal container. Finish cleaning by spreading water on the contaminated surface and allow to evacuate through the sanitary system.

  • Handling and storage: Avoid contact with skin and eyes. Avoid formation of dust and aerosols. Avoid exposure - obtain special instructions before use.Provide appropriate exhaust ventilation at places where dust is formed. For precautions see section 2.2. Precautions: Keep away from heat. Keep away from sources of ignition. Ground all equipment containing material. Do not ingest. Do not breathe dust. If ingested, seek medical advice immediately and show the container or the label. Keep away from incompatibles such as oxidizing agents. Storage: Keep container tightly closed. Keep container in a cool, well-ventilated area. Sensitive to light. Store in light-resistant containers.

  • Exposure controls/personal protection:Occupational Exposure limit valuesBiological limit values Handle in accordance with good industrial hygiene and safety practice. Wash hands before breaks and at the end of workday. Eye/face protection Safety glasses with side-shields conforming to EN166. Use equipment for eye protection tested and approved under appropriate government standards such as NIOSH (US) or EN 166(EU). Skin protection Wear impervious clothing. The type of protective equipment must be selected according to the concentration and amount of the dangerous substance at the specific workplace. Handle with gloves. Gloves must be inspected prior to use. Use proper glove removal technique(without touching glove's outer surface) to avoid skin contact with this product. Dispose of contaminated gloves after use in accordance with applicable laws and good laboratory practices. Wash and dry hands. The selected protective gloves have to satisfy the specifications of EU Directive 89/686/EEC and the standard EN 374 derived from it. Respiratory protection Wear dust mask when handling large quantities. Thermal hazards

Supplier and reference price

  • Manufacture/Brand
  • Product Description
  • Packaging
  • Price
  • Delivery
  • Purchase
  • Manufacture/Brand:TRC
  • Product Description:Azelaic acid
  • Packaging:25g
  • Price:$ 130
  • Delivery:In stock
  • Buy Now
  • Manufacture/Brand:Sigma-Aldrich
  • Product Description:Azelaic acid technical, ~85% (GC)
  • Packaging:50g
  • Price:$ 24
  • Delivery:In stock
  • Buy Now
  • Manufacture/Brand:Sigma-Aldrich
  • Product Description:Azelaic acid, technical grade for synthesis. CAS No. 123-99-9, EC Number 204-669-1., technical grade for synthesis
  • Packaging:8201160100
  • Price:$ 34.8
  • Delivery:In stock
  • Buy Now
  • Manufacture/Brand:Sigma-Aldrich
  • Product Description:Azelaic acid, technical grade for synthesis
  • Packaging:100 g
  • Price:$ 33.3
  • Delivery:In stock
  • Buy Now
  • Manufacture/Brand:Sigma-Aldrich
  • Product Description:Azelaic acid for synthesis. CAS 123-99-9, molar mass 188.22 g/mol., for synthesis
  • Packaging:8201170025
  • Price:$ 61.5
  • Delivery:In stock
  • Buy Now
  • Manufacture/Brand:Sigma-Aldrich
  • Product Description:Azelaic acid for synthesis
  • Packaging:25 g
  • Price:$ 58.92
  • Delivery:In stock
  • Buy Now
  • Manufacture/Brand:Sigma-Aldrich
  • Product Description:Azelaic acid 98%
  • Packaging:25g
  • Price:$ 53.3
  • Delivery:In stock
  • Buy Now
  • Manufacture/Brand:Sigma-Aldrich
  • Product Description:Azelaic acid technical, ~85% (GC)
  • Packaging:250g
  • Price:$ 52.4
  • Delivery:In stock
  • Buy Now
  • Manufacture/Brand:Sigma-Aldrich
  • Product Description:Azelaic acid, technical grade for synthesis. CAS No. 123-99-9, EC Number 204-669-1., technical grade for synthesis
  • Packaging:8201161000
  • Price:$ 80.4
  • Delivery:In stock
  • Buy Now
  • Manufacture/Brand:Sigma-Aldrich
  • Product Description:Azelaic acid, technical grade for synthesis
  • Packaging:1 kg
  • Price:$ 76.96
  • Delivery:In stock
  • Buy Now

Relevant articles and documentsAll total 90 Articles be found

Lapworth,Mottram

, p. 1987 (1925)

A New and Efficient Approach to Macrocyclic Keto Lactones

Karim, Mohammad R.,Sampson, Paul

, p. 598 - 605 (1990)

A new and efficient method for macrolactonization has been developed.The intramolecular nucleophilic displacement of chloride from the highly electrophilic α-chloro ketone moiety in 15 by a remote carboxylate nucleophile resulted in the clean formation of the 11-membered keto lactone 1.Relatively high substrate concentrations (up to 18 mM) could be employed without formation of dimeric or oligomeric byproducts.The slow mixing of substrate and base was not required.This macrolactonization reaction was studied in various solvents at a number of substrate concentrations and reaction temperatures in order to evaluate its scope and limitations.A low-temperature Ti(III) ion/peroxide induced radical addition reaction has been developed.The lowering of the reaction temperature from 0 deg C to -78 deg C consistently afforded a dramatic increase in product yield from such reactions.This lowering of the reaction temperature proved essential when the highly functionalized acetoxymethyl vinyl ketone was employed as the radical acceptor.

γ-hydroxyalkenals are oxidatively cleaved through Michael addition of acylperoxy radicals and fragmentation of intermediate β-hydroxyperesters

Balamraju, Yuvaraju N.,Sun, Mingjiang,Salomon, Robert G.

, p. 11522 - 11528 (2004)

Oxidative cleavage of arachidonate (C20) and linoleate (C 18) phospholipids generates truncated C8 or C12 γ-hydroxyalkenal phospholipids as well as C5 or C9 carboxyalkanoate phospholipids,

Microbial synthesis of medium-chain α,ω-dicarboxylic acids and ω-aminocarboxylic acids from renewable long-chain fatty acids

Song, Ji-Won,Lee, Jung-Hoo,Bornscheuer, Uwe T.,Park, Jin-Byung

, p. 1782 - 1788 (2014)

Biotransformation of long-chain fatty acids into medium-chain α,ω-dicarboxylic acids or ω-aminocarboxylic acids could be achieved with biocatalysts. This study presents the production of α,ω-dicarboxylic acids (e.g., C9, C11, C 12, C13) and ω-aminocarboxylic acids (e.g., C 11, C12, C13) directly from fatty acids (e.g., oleic acid, ricinoleic acid, lesquerolic acid) using recombinant Escherichia coli-based biocatalysts. ω-Hydroxycarboxylic acids, which were produced from oxidative cleavage of fatty acids via enzymatic reactions involving a fatty acid double bond hydratase, an alcohol dehydrogenase, a Baeyer-Villiger monooxygenase and an esterase, were then oxidized to α,ω- dicarboxylic acids by alcohol dehydrogenase (ADH, AlkJ) from Pseudomonas putida GPo1 or converted into ω-aminocarboxylic acids by a serial combination of ADH from P. putida GPo1 and an ω-transaminase of Silicibacter pomeroyi. The double bonds present in the fatty acids such as ricinoleic acid and lesquerolic acid were reduced by E. coli-native enzymes during the biotransformations. This study demonstrates that the industrially relevant building blocks (C9 to C13 saturated α,ω- dicarboxylic acids and ω-aminocarboxylic acids) can be produced from renewable fatty acids using biocatalysis.

Preparation, characterization, and theoretical studies of azelaic acid derived from oleic acid by use of a novel ozonolysis method

Kadhum, Abdul Amir H.,Wasmi, Bilal A.,Mohamad, Abu Bakar,Al-Amiery, Ahmed A.,Takriff, Mohd S.

, p. 659 - 668 (2012)

Environmentally friendly manufacture of organic compounds has been intensively reexamined in recent years. Many excellent methods have been devised to produce organic compounds from renewable resources. Azelaic acid has been produced by ozonolysis of oleic acid. The reaction was performed in a Bach bubbling reactor, with fine bubbles, at high temperature (150 °C) without utilizing any catalyst or any solvent. Yield of the reaction was 20% after 2 h. Production of azelaic acid was confirmed by use of FT-IR and 1H NMR spectroscopic data and high-performance liquid chromatography of both synthesized and reference azelaic acid. A theoretical study was performed to obtain quantum chemical data for azelaic acid and to optimize the molecule's geometry. Springer Science+Business Media B.V. 2011.

-

Barger et al.

, p. 90,93 (1933)

-

-

Acker,Anderson

, p. 1162 (1959)

-

-

Gunstone,F.D. et al.

, p. 295 - 296 (1967)

-

Thermoplastic polyester amides derived from oleic acid

Zuo, Jiaqing,Li, Shaojun,Bouzidi, Laziz,Narine, Suresh S.

, p. 4503 - 4516 (2011)

Three lipid-based Polyester Amides (PEAs) with varying ratios of ester and amide linkages were synthesized. Oleic acid was used as the starting material to produce the intermediates, characterized by MS and NMR, used for polymerization. PEAs were characterized by FTIR and GPC. The PEAs were constrained to have similar number average molecular weights, in the 2 × 104 range, thereby enabling comparison of their physical properties from a structural perspective. The thermal behavior of the polymers was assessed by DSC, DMA and TGA. Thermal degradation was not affected by ester/amide ratios, but Tg increased non-linearly with decreasing ester/amide ratios and correlated with hydrogen-bond density and repeating unit chain length. Crystallinity was studied by XRD and DSC. Degree of crystallization and multiple melting behavior as a function of cooling kinetics were explained well by hydrogen-bond density, repeating unit chain length and density of ester moieties. Mechanical properties were investigated by DMA and Tensile Analysis, with a non-linear increase of storage and tensile moduli recorded as a function of decreasing ester/amide ratios. The findings suggest how approaches to the synthesis of lipid-based PEAs can be targeted to the delivery of specific physical properties.

Applewhite,T.H. et al.

, p. 3407 - 3409 (1966)

-

Nunn,Smedley-Maclean

, p. 2744 (1935)

-

Simultaneous Enzyme/Whole-Cell Biotransformation of C18 Ricinoleic Acid into (R)-3-Hydroxynonanoic Acid, 9-Hydroxynonanoic Acid, and 1,9-Nonanedioic Acid

Cha, Hee-Jeong,Seo, Eun-Ji,Song, Ji-Won,Jo, Hye-Jin,Kumar, Akula Ravi,Park, Jin-Byung

, p. 696 - 703 (2018)

Regiospecific oxyfunctionalization of renewable long chain fatty acids into industrially relevant C9 carboxylic acids has been investigated. One example was biocatalytic transformation of 10,12-dihydroxyoctadecanoic acid, which was produced from ricinoleic acid ((9Z,12R)-12-hydroxyoctadec-9-enoic acid) by a fatty acid double bond hydratase, into (R)-3-hydroxynonanoic acid, 9-hydroxynonanoic acid, and 1,9-nonanedioic acid with a high conversion yield of ca. 70%. The biotransformation was driven by enzyme/whole-cell biocatalysts, consisting of the esterase of Pseudomonas fluorescens and the recombinant Escherichia coli expressing the secondary alcohol dehydrogenase of Micrococcus luteus, the Baeyer-Villiger monooxygenase of Pseudomonas putida KT2440 and the primary alcohol/aldehyde dehydrogenases of Acinetobacter sp. NCIMB9871. The high conversion yields and the high product formation rates over 20 U/g dry cells with insoluble reactants indicated that various (poly-hydroxy) fatty acids could be converted into multi-functional products via the simultaneous enzyme/whole-cell biotransformations. This study will contribute to the enzyme-based functionalization of hydrophobic substances. (Figure presented.).

Scalable, sustainable and catalyst-free continuous flow ozonolysis of fatty acids

Atapalkar, Ranjit S.,Athawale, Paresh R.,Srinivasa Reddy,Kulkarni, Amol A.

supporting information, p. 2391 - 2396 (2021/04/07)

A simple and efficient catalyst-free protocol for continuous flow synthesis of azelaic acid is developed from the renewable feedstock oleic acid. An ozone and oxygen mixture was used as the reagent for oxidative cleavage of double bond without using any metal catalyst or terminal oxidant. The target product was scaled up to more than 100 g with 86% yield in a white powder form. Complete recycling and reuse of the solvent were established making it a green method. The approach is significantly energy efficient and also has a very small chemical footprint. The methodology has been successfully tested with four fatty acids making it a versatile platform that gives value addition from renewable resources.

FLOW CHEMISTRY SYNTHESIS OF ISOCYANATES

-

Paragraph 0008; 0175; 0180, (2021/06/22)

The disclosure provides, inter alia, safe and environmentally-friendly methods, such as flow chemistry, to synthesize isocyanates, such as methylene diphenyl diisocyanate, toluene diisocyanate, hexamethylene diisocyanate, isophorone diisocyanate, and tetramethylxylene diisocyanate.

METHOD FOR MANUFACTURING PELARGONIC ACID AND AZELAIC ACID

-

Paragraph 0055-0083, (2021/07/27)

The present invention relates to a method for producing pelargonic acid and azelaic acid, and more specifically, provides a method for producing pelargonic acid and azelaic acid, which comprises the following steps of: a) reacting an unsaturated carboxylic acid compound under a tungstic acid catalyst to obtain an intermediate product comprising vicinal diol; and b) reacting the intermediate product under a transition metal hydroxide catalyst to obtain the pelargonic acid and azelaic acid. The production method is capable of producing the pelargonic acid and azelaic acid in a high yield from the unsaturated carboxylic acid compound.

Oxidative carbon-carbon bond cleavage of 1,2-diols to carboxylic acids/ketones by an inorganic-ligand supported iron catalyst

Chen, Weiming,Xie, Xin,Zhang, Jian,Qu, Jian,Luo, Can,Lai, Yaozhu,Jiang, Feng,Yu, Han,Wei, Yongge

, p. 9140 - 9146 (2021/11/23)

The carbon-carbon bond cleavage of 1,2-diols is an important chemical transformation. Although traditional stoichiometric and catalytic oxidation methods have been widely used for this transformation, an efficient and valuable method should be further explored from the views of reusable catalysts, less waste, and convenient procedures. Herein an inorganic-ligand supported iron catalyst (NH4)3[FeMo6O18(OH)6]·7H2O was described as a heterogeneous molecular catalyst in acetic acid for this transformation in which hydrogen peroxide was used as the terminal oxidant. Under the optimized reaction conditions, carbon-carbon bond cleavage of 1,2-diols could be achieved in almost all cases and carboxylic acids or ketones could be afforded with a high conversion rate and high selectivity. Furthermore, the catalytic system was used efficiently to degrade renewable biomass oleic acid. Mechanistic insights based on the observation of the possible intermediates and control experiments are presented.

Process for preparing azelaic acid

-

Paragraph 0105-0108, (2021/02/19)

A process for preparing azelaic acid is disclosed. In particular, the process for preparing azelaic acid is an ozone free process. The process for preparing azelaic acid comprises a step of decarboxylation of tetra-carboxylic acid in the presence of a organic sulfonic acid.

Process route upstream and downstream products

Process route

hydrogenchloride
7647-01-0,15364-23-5

hydrogenchloride

12-hydroxy-9-hydroxyimino-octadecanoic acid

12-hydroxy-9-hydroxyimino-octadecanoic acid

azelaic acid
123-99-9,26776-28-3

azelaic acid

8-Aminooctanoic acid
1002-57-9

8-Aminooctanoic acid

Conditions
Conditions Yield
at 190 ℃;
9-hydroxyimino-heptadecanoic acid

9-hydroxyimino-heptadecanoic acid

sulfuric acid
7664-93-9

sulfuric acid

azelaic acid
123-99-9,26776-28-3

azelaic acid

n-Octylamine
111-86-4

n-Octylamine

8-Aminooctanoic acid
1002-57-9

8-Aminooctanoic acid

Conditions
Conditions Yield
Erhitzen mit konz. Salzsaeure auf 180grad.Hydrolysis;
1,3-Dioxa-cyclododecane-4,12-dione

1,3-Dioxa-cyclododecane-4,12-dione

azelaic acid
123-99-9,26776-28-3

azelaic acid

1,9-Nonanediol
3937-56-2

1,9-Nonanediol

9-hydroxynonanoic acid
3788-56-5

9-hydroxynonanoic acid

Conditions
Conditions Yield
With sodium tetrahydroborate; In tetrahydrofuran; at 23 ℃; for 120h;
2%
92%
With sodium tetrahydroborate; In tetrahydrofuran; at 65 ℃; for 6h;
87%
6%
10,12-dihydroxyoctadecanoic acid

10,12-dihydroxyoctadecanoic acid

azelaic acid
123-99-9,26776-28-3

azelaic acid

(R)-3-hydroxynonanoic acid
33796-87-1

(R)-3-hydroxynonanoic acid

9-hydroxynonanoic acid
3788-56-5

9-hydroxynonanoic acid

C<sub>18</sub>H<sub>34</sub>O<sub>5</sub>

C18H34O5

Conditions
Conditions Yield
With alcohol dehydrogenase of Micrococcus luteus; alcohol/aldehyde dehydrogenases of Acinetobacter sp. NCIMB9871; esterase of Pseudomonas fluorescens; recombinant Baeyer-Villiger monooxygenase of Pseudomonas putida KT2440; recombinant long chain fatty acid transporter; at 35 ℃; pH=8; regiospecific reaction; Microbiological reaction; Enzymatic reaction;
220 mg
240 mg
azelaic acid
123-99-9,26776-28-3

azelaic acid

9-hydroxynonanoic acid
3788-56-5

9-hydroxynonanoic acid

Conditions
Conditions Yield
Multi-step reaction with 2 steps
1: recombinant fatty acid double bond hydratase of Stenotrophomonas maltophilia; water / 3 h / 35 °C / pH 8 / Microbiological reaction; Enzymatic reaction
2: alcohol dehydrogenase of Micrococcus luteus; recombinant Baeyer-Villiger monooxygenase of Pseudomonas putida KT2440; recombinant long chain fatty acid transporter; alcohol/aldehyde dehydrogenases of Acinetobacter sp. NCIMB9871; esterase of Pseudomonas fluorescens / 35 °C / pH 8 / Microbiological reaction; Enzymatic reaction
With alcohol dehydrogenase of Micrococcus luteus; alcohol/aldehyde dehydrogenases of Acinetobacter sp. NCIMB9871; esterase of Pseudomonas fluorescens; recombinant Baeyer-Villiger monooxygenase of Pseudomonas putida KT2440; recombinant fatty acid double bond hydratase of Stenotrophomonas maltophilia; recombinant long chain fatty acid transporter; water;
azelaic acid
123-99-9,26776-28-3

azelaic acid

(3Z)-dodecene-1,12-dioic acid
189034-80-8

(3Z)-dodecene-1,12-dioic acid

9-hydroxynonanoic acid
3788-56-5

9-hydroxynonanoic acid

(12Z)-9-hydroxy-10-oxo-12-octadecenoic acid
5503-03-7,70144-92-2,26369-27-7

(12Z)-9-hydroxy-10-oxo-12-octadecenoic acid

13-hydroxy-12-oxo-octadeca-cis-9-enoic acid
5502-89-6

13-hydroxy-12-oxo-octadeca-cis-9-enoic acid

(9Z)-11-hydroxy-12,13-epoxy-9-octadecenoic acid

(9Z)-11-hydroxy-12,13-epoxy-9-octadecenoic acid

(4Z)-2-pentyl-4-tridecene-1,13-dioic acid

(4Z)-2-pentyl-4-tridecene-1,13-dioic acid

(2’Z)-2-(2’-octenyl)-decane-1,10-dioic acid

(2’Z)-2-(2’-octenyl)-decane-1,10-dioic acid

(2’Z,5’Z)-2-(2’,5’-octadienyl)-decane-1,10-dioic acid

(2’Z,5’Z)-2-(2’,5’-octadienyl)-decane-1,10-dioic acid

(12Z)-10-oxo-11-hydroxy-12-octadecenoic acid

(12Z)-10-oxo-11-hydroxy-12-octadecenoic acid

(13S,9Z,11E)-13-hydroxy-9,11-octadecadienoic acid
29623-28-7

(13S,9Z,11E)-13-hydroxy-9,11-octadecadienoic acid

(9S,10E,12Z)-9-hydroxy-10,12-octadecadienoic acid
73543-67-6

(9S,10E,12Z)-9-hydroxy-10,12-octadecadienoic acid

Conditions
Conditions Yield
With oxygen; for 0.5h; Enzymatic reaction;
Methyl oleate
112-62-9

Methyl oleate

azelaic acid
123-99-9,26776-28-3

azelaic acid

heptanedioic acid
111-16-0

heptanedioic acid

octane-1,8-dioic acid
505-48-6

octane-1,8-dioic acid

Octanoic acid
124-07-2

Octanoic acid

nonanoic acid
112-05-0

nonanoic acid

Conditions
Conditions Yield
With 7CeO2*7Nb2O5*3La2O3*K2O*2Bi2O3; oxygen; at 120 ℃; for 15h; under 6750.68 Torr; Autoclave;
27.5%
17.5%
6.8%
17.6%
11.4%
Methyl oleate
112-62-9

Methyl oleate

azelaic acid
123-99-9,26776-28-3

azelaic acid

octane-1,8-dioic acid
505-48-6

octane-1,8-dioic acid

oenanthic acid
111-14-8

oenanthic acid

Octanoic acid
124-07-2

Octanoic acid

nonanoic acid
112-05-0

nonanoic acid

Conditions
Conditions Yield
With 0.5CeO2*Nb2O5; oxygen; at 120 ℃; for 15h; under 6750.68 Torr; Reagent/catalyst; Autoclave;
19.8%
11%
16.6%
10.9%
5.3%
9,10-diketostearic acid
656-73-5

9,10-diketostearic acid

azelaic acid
123-99-9,26776-28-3

azelaic acid

octane-1,8-dioic acid
505-48-6

octane-1,8-dioic acid

nonanoic acid
112-05-0

nonanoic acid

Conditions
Conditions Yield
With 1 wt% Au/Al2O3; oxygen; sodium hydroxide; In water; at 80 ℃; for 4.33333h; under 3750.38 Torr; Autoclave; Inert atmosphere;
28%
Methyl oleate
112-62-9

Methyl oleate

azelaic acid
123-99-9,26776-28-3

azelaic acid

octane-1,8-dioic acid
505-48-6

octane-1,8-dioic acid

Octanoic acid
124-07-2

Octanoic acid

nonanoic acid
112-05-0

nonanoic acid

Conditions
Conditions Yield
With 7CeO2*7Nb2O5*3La2O3*K2O*2Bi2O3; oxygen; at 120 ℃; for 15h; under 30003 Torr; Reagent/catalyst; Temperature; Pressure; Catalytic behavior; Autoclave;
8.2%
12.5%
5.7%
8.5%

Global suppliers and manufacturers

Global( 259) Suppliers
  • Company Name
  • Business Type
  • Contact Tel
  • Emails
  • Main Products
  • Country
  • Greenutra Resource Inc
  • Business Type:Trading Company
  • Contact Tel:0086-411-39553357
  • Emails:sales@greenutra.cn
  • Main Products:33
  • Country:China (Mainland)
  • Chemwill Asia Co., Ltd.
  • Business Type:Manufacturers
  • Contact Tel:021-51086038
  • Emails:sales@chemwill.com
  • Main Products:30
  • Country:China (Mainland)
  • Hangzhou Dingyan Chem Co., Ltd
  • Business Type:Manufacturers
  • Contact Tel:86-571-86465881,86-571-87157530,86-571-88025800
  • Emails:sales@dingyanchem.com
  • Main Products:95
  • Country:China (Mainland)
  • Simagchem Corporation
  • Business Type:Manufacturers
  • Contact Tel:+86-592-2680277
  • Emails:sale@simagchem.com
  • Main Products:110
  • Country:China (Mainland)
  • GIHI CHEMICALS CO.,LIMITED
  • Business Type:Lab/Research institutions
  • Contact Tel:571-86217390
  • Emails:info@gihichem.com
  • Main Products:66
  • Country:China (Mainland)
  • Kono Chem Co.,Ltd
  • Business Type:Other
  • Contact Tel:86-29-86107037-8015
  • Emails:info@konochemical.com
  • Main Products:83
  • Country:China (Mainland)
close
Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 123-99-9
Post Buying Request Now
close
Remarks: The blank with*must be completed