Azelaic acid - Moligand™, ≥99% , CAS No.123-99-9

CAS: 123-99-9 Cat. No.: A108439 Molecular Weight: 188.22 Beilstein Registry Number: 1101094 EC Number: 204-669-1
AVAILABLE TO ORDER
GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. ≥99%
Synonyms
DTXSID8021640 | Azelex | Finacea Foam | MLS000069659 | Acido azelaico | MLS001148615 | Emerox 1110 | Finevin | KBioGR_000662 | Lopac0_000051 | Nonandisaure | Anchoate | SR-01000075671 | NONANEDIOIC ACID | 1,7-Heptanedicarboxylic Acid | Nonanedioic Acid
Storage
Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
25g
A108439-25g
3
$9.90
100g
A108439-100g
7
$17.90
500g
A108439-500g
5
$52.90
Enter a quantity for the sizes you want to add.
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Why this grade

Moligand™, ≥99% Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature Ships Normal Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 24 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

Azelaic acid is a dicarboxylic acid that exhibits anti-inflammatory activity. It is known for it’s anti acne activity in vitro. Azelaic acid directly inhibits kallikrein 5 (KLK5), downregulating expression of KLK5, toll-like receptor 2 (TLR 2), and cathelicidin, and suppresses activity of serine proteases in vitro, in vivo, and in clinical settings. In PUFA-treated fibroblasts, azelaic acid decreases generation of ROS and upregulates expression of antioxidative enzymes, inhibiting cell damage; agonist activity at PPARν is thought to drive these effects. Azelaic acid also inhibits proliferation of melanocytes. This compound displays antiacne and anticancer potential as well, inhibiting the proliferation of cutaneous melanoma due to suppression of mitochondrial oxidoreductive activity and DNA synthesis.
An antiinflammatory compound

Specifications

Synonyms
DTXSID8021640 | Azelex | Finacea Foam | MLS000069659 | Acido azelaico | MLS001148615 | Emerox 1110 | Finevin | KBioGR_000662 | Lopac0_000051 | Nonandisaure | Anchoate | SR-01000075671 | NONANEDIOIC ACID | 1, 7-Heptanedicarboxylic Acid | Nonanedioic Acid
Specifications & Purity
Moligand™, ≥99%
Biochemical and Physiological Mechanisms
5α reductase inhibitor. PPARγ activator. Competitively inhibits tyrosinase and thioredoxin reductase (K i values are 3 mM and 13 μM respectively). Cytotoxin to melanocytes. Reduces skin hyperpigmentation. Induces salicylic acid accumulation in plants.
Storage
Room temperature
Shipped In
Normal
Grade
Moligand™
Note
Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Purity
≥99%
Product Properties
ALogP1.6
Names and Identifiers
Pubchem Sid488179683
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488179683
Canonical SmilesC(CCCC(=O)O)CCCC(=O)O
IUPAC Namenonanedioic acid
InChIKeyBDJRBEYXGGNYIS-UHFFFAOYSA-N
INCHI1S/C9H16O4/c10-8(11)6-4-2-1-3-5-7-9(12)13/h1-7H2,(H,10,11)(H,12,13)
Isomeric SMILES C(CCCC(=O)O)CCCC(=O)O
WGK Germany 1
RTECS CM1980000
Molecular Weight 188.22
Beilstein 1101094
Reaxy-Rn 1101094
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1101094&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassLipids and lipid-like molecules
ClassFatty Acyls
SubclassFatty acids and conjugates
Intermediate Tree Nodes Not available
Direct ParentMedium-chain fatty acids
Alternative Parents Dicarboxylic acids and derivatives  Carboxylic acids  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic acyclic compounds
Substituents Medium-chain fatty acid - Dicarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound
DescriptionThis compound belongs to the class of organic compounds known as medium-chain fatty acids. These are fatty acids with an aliphatic tail that contains between 4 and 12 carbon atoms.
External Descriptors Dicarboxylic acids
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
ESR1 Tclin Estrogen receptor alpha (17718 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NR3C1 Tclin Glucocorticoid receptor (14987 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PGR Tclin Progesterone receptor (8562 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRB2 Tclin Beta-2 adrenergic receptor (11824 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CHRM2 Tclin Muscarinic acetylcholine receptor M2 (10671 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRB1 Tclin Beta-1 adrenergic receptor (6630 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HTR1A Tclin Serotonin 1a (5-HT1a) receptor (14969 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRA2A Tclin Alpha-2a adrenergic receptor (9450 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AR Tclin Androgen Receptor (11781 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CHRM1 Tclin Muscarinic acetylcholine receptor M1 (12690 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
DRD2 Tclin Dopamine D2 receptor (23596 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GABRA1 Tclin GABA receptor alpha-1 subunit (399 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TSHR Tclin Thyroid stimulating hormone receptor (29986 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MAOA Tclin Monoamine oxidase A (11911 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CNR1 Tclin Cannabinoid CB1 receptor (20913 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
DRD1 Tclin Dopamine D1 receptor (9720 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PTGS1 Tclin Cyclooxygenase-1 (9233 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC6A2 Tclin Norepinephrine transporter (10102 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HRH2 Tclin Histamine H2 receptor (5428 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HTR2A Tclin Serotonin 2a (5-HT2a) receptor (14758 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HTR2C Tclin Serotonin 2c (5-HT2c) receptor (11471 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AVPR2 Tclin Vasopressin V2 receptor (2912 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADORA1 Tclin Adenosine A1 receptor (17603 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AGTR1 Tclin Type-1 angiotensin II receptor (5176 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC6A4 Tclin Serotonin transporter (12625 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRA1A Tclin Alpha-1a adrenergic receptor (8359 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PTGS2 Tclin Cyclooxygenase-2 (13999 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HRH1 Tclin Histamine H1 receptor (7573 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
OPRM1 Tclin Mu opioid receptor (19785 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
DRD3 Tclin Dopamine D3 receptor (14368 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AVPR1A Tclin Vasopressin V1a receptor (5412 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
OPRD1 Tclin Delta opioid receptor (15096 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
OPRK1 Tclin Kappa opioid receptor (16155 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HTR3A Tclin Serotonin 3a (5-HT3a) receptor (3366 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC6A3 Tclin Dopamine transporter (10535 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GRIN1 Tclin Glutamate (NMDA) receptor subunit zeta 1 (122 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KCNH2 Tclin HERG (29587 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CACNA1C Tclin Voltage-gated L-type calcium channel alpha-1C subunit (766 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PDE3A Tclin Phosphodiesterase 3A (3309 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC29A1 Tclin Equilibrative nucleoside transporter 1 (1711 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRA2B Tclin Alpha-2b adrenergic receptor (4412 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRA2C Tclin Alpha-2c adrenergic receptor (4876 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CHRM3 Tclin Muscarinic acetylcholine receptor M3 (7750 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HTR2B Tclin Serotonin 2b (5-HT2b) receptor (10323 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TBXA2R Tclin Thromboxane A2 receptor (5717 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADORA2A Tclin Adenosine A2a receptor (16305 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADORA3 Tchem Adenosine A3 receptor (15931 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
BDKRB2 Tclin Bradykinin B2 receptor (3970 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CHRNA4 Tclin Neuronal acetylcholine receptor protein alpha-4 subunit (1265 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ARSA Tbio Cerebroside-sulfatase (655 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
ampC Beta-lactamase AmpC (62480 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mc4r Melanocortin receptor 4 (1205 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Npy1r Neuropeptide Y receptor type 1 (8 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cckar Cholecystokinin A receptor (90 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Pde4d Phosphodiesterase 4D (4 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Hdac6 Histone deacetylase 6 (222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
pfk 6-phospho-1-fructokinase (7870 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ffp 4'-phosphopantetheinyl transferase ffp (24982 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
FTL Ferritin light chain (43324 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mechanisms of Action
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

28 results found

Lot NumberCertificate TypeDateItem
D2621170Certificate of AnalysisMar 07, 2026 A108439
D2621167Certificate of AnalysisMar 07, 2026 A108439
K2427338Certificate of AnalysisNov 25, 2024 A108439
K2422350Certificate of AnalysisNov 25, 2024 A108439
A2503074Certificate of AnalysisNov 16, 2024 A108439
H2508049Certificate of AnalysisNov 16, 2024 A108439
A2503073Certificate of AnalysisNov 16, 2024 A108439
G2422469Certificate of AnalysisSep 14, 2023 A108439
J2419005Certificate of AnalysisSep 14, 2023 A108439
J2408278Certificate of AnalysisSep 14, 2023 A108439
J2312103Certificate of AnalysisSep 14, 2023 A108439
B2626048Certificate of AnalysisSep 14, 2023 A108439
E2324576Certificate of AnalysisMay 06, 2023 A108439
E2324575Certificate of AnalysisMay 06, 2023 A108439
E2324574Certificate of AnalysisMay 06, 2023 A108439
E2324569Certificate of AnalysisMay 06, 2023 A108439
B2324339Certificate of AnalysisJul 14, 2022 A108439
J2210122Certificate of AnalysisJul 14, 2022 A108439
J2210123Certificate of AnalysisJul 14, 2022 A108439
J2210124Certificate of AnalysisJul 14, 2022 A108439
J2210128Certificate of AnalysisJul 14, 2022 A108439
E2311091Certificate of AnalysisJul 14, 2022 A108439
B2324338Certificate of AnalysisJul 14, 2022 A108439
F2215186Certificate of AnalysisJun 05, 2022 A108439
F2215187Certificate of AnalysisJun 05, 2022 A108439
F2215322Certificate of AnalysisJun 05, 2022 A108439
E1803118Certificate of AnalysisMar 30, 2022 A108439
F2129092Certificate of AnalysisJul 03, 2021 A108439

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Chemical and Physical Properties
SolubilitySoluble in water (2.4 mg/ml at 20 °C), ethanol (5%), DMSO, methanol (70 mg/ml), and alcohol.
SensitivityMoisture sensitive.
Refractive Index1.4303
Flash Point(°F)410 °F
Flash Point(°C)210 °C
Boil Point(°C)286°C
Melt Point(°C)109-111°C
Molecular Weight188.220 g/mol
XLogP31.600
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count4
Rotatable Bond Count8
Exact Mass188.105 Da
Monoisotopic Mass188.105 Da
Topological Polar Surface Area74.600 Ų
Heavy Atom Count13
Formal Charge0
Complexity147.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Documents & Articles
Citations of This Product
References
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2. Qi Jing, Jin Feiyang, You Yuchan, Du Yan, Liu Di, Xu Xiaoling, Wang Jun, Zhu Luwen, Chen Minjiang, Shu Gaofeng, Wu Liming, Ji Jiansong, Du Yongzhong.  (2021)  Synergistic effect of tumor chemo-immunotherapy induced by leukocyte-hitchhiking thermal-sensitive micelles.  Nature Communications,  12  (1): (1-17).  [PMID:34362890] [10.1038/s41467-021-24902-2]
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8. Wanjing Zhang, Liyan Wang, Yunsheng Chong, Wei Liu, Xin Qian.  (2025)  Development of biocompatible azelaic acid-based copolyester plasticizers for PVC applications.  POLYMER,      [PMID:] [10.1016/j.polymer.2025.128322]
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11. Zhengyu Zhou, Bingbing Shi, Chengxin Zhang, Yiyun Wang, Pengfei Tang, Jiajun Feng, Jingjing Fan, Feng Jiang, Yongliang Ding.  (2024)  High-performance sustainable polyester amide composites with persistent luminescence for multiple anti-counterfeiting.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2024.159007]
12. Ling Chen, Zhou Rudong, Xiang Yanli, Fang Jianbo, Meng Xu, Ren Qiang, Wang Chenyi.  (2024)  Solvent-free flexible epoxy intumescent fire-retardant coatings.  Journal of Coatings Technology and Research,      [PMID:] [10.1007/s11998-024-00918-3]
13. Yongliang Ding, Chengxin Zhang, Bingbing Shi, Yiyun Wang, Pengfei Tang, Cheng Liu, Jingjing Fan, Zhongkai Wang, Feng Jiang.  (2024)  Sustainable ultra-strong polyesteramide elastomers with rapid degradation and high resilience.  EUROPEAN POLYMER JOURNAL,      [PMID:] [10.1016/j.eurpolymj.2024.112901]
14. Wanjing Zhang, Yuqi Shan, Liyan Wang, Yanming Chen, Liying Guo, Yunsheng Chong, Xin Qian.  (2025)  Synthesis of 2-Methyl-1,3-Propanediol Modified Azelaic Acid-Octanediol Copolyester Plasticizers and Their Plasticizing Effect on Polyvinyl Chloride.  JOURNAL OF APPLIED POLYMER SCIENCE,      [PMID:] [10.1002/app.56849]
15. Wanjing Zhang, Liyan Wang, Hong Chen, Liying Guo, Yaoyao Bai, Xin Qian.  (2024)  Synthesis of azelaic acid copolyester plasticizers and their application in PVC.  RSC Advances,  14  (33): (23662-23671).  [PMID:39077328] [10.1039/D4RA03174A]
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17. Yiquan Wang, Yuxiang Liang, Yiya Li, Wenqi Rui, Jingjian He, Mengya Zhao.  (2024)  Synthesis, tribological properties and oxidative stability of polyol esters base oils containing pentaerythritol complex esters.  TRIBOLOGY INTERNATIONAL,      [PMID:] [10.1016/j.triboint.2024.109618]
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19. Wang Guoqiang, Yu Yiheng, Zhang Mengke, Shi Longqing, Hu Hongliang, Jin Yujie, Hu Jing.  (2025)  1,4-Cyclohexanedimethanol-based polyesters derived from 1,4-cyclohexanedimethanol (CHDM) and aliphatic diacids with odd carbons.  POLYMER BULLETIN,      [PMID:] [10.1007/s00289-025-05887-0]
20. Dequan Chi, Chao Wu, Haoyu Gu, Xinchao Sun, Ruoxi Zhao, Dongjie Zhang, Zhimin Xie, Zhongjun Cheng, Yuyan Liu.  (2025)  Tailored cocrystal architectures enable highly reversible actuation in crystalline polymer networks.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2025.169166]
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23. Zhou Xiaorui, Yang Ying, Lv Chang, Cheng Xinru, Hao Wenbo, Su Tingting, Huang Chenhao, Hu Bing.  (2026)  Influence of Carbon Chain Length and Odd–Even Effect on the Properties of Azelaic Acid-Based Aliphatic Polyesters.  JOURNAL OF POLYMERS AND THE ENVIRONMENT,  34  (4): (80).  [PMID:] [10.1007/s10924-026-03770-1]
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