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10-Undecenoic acid - 98%, high purity , CAS No.112-38-9

  • ≥98%
Item Number
U106484
Grouped product items
SKUSizeAvailabilityPrice Qty
U106484-100ml
100ml
In stock
$22.90
U106484-250ml
250ml
In stock
$50.90
U106484-500ml
500ml
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$74.90
View related series
Carbonyl compound carboxylic acid

Basic Description

Synonymsundecylenic acid|10-UNDECENOIC ACID|Undec-10-enoic acid|112-38-9|Undecenoic acid|10-Hendecenoic acid|Desenex|Renselin|Sevinon|Declid|9-Undecylenic acid|10-Undecylenic acid|Undecyl-10-enic acid|FEMA No. 3247|undecylenate|Kyselina undecylenova|Caswell No. 9
Specifications & Purity≥98%
Shipped InNormal

Associated Targets

DRD1 Tclin D(1A) dopamine receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ESR1 Tclin Estrogen receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

GABRA1 Tclin Gamma-aminobutyric acid receptor subunit alpha-1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

HRH3 Tclin Histamine H3 receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

HDAC6 Tclin Histone deacetylase 6 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

SLC6A2 Tclin Sodium-dependent noradrenaline transporter 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

SLC6A3 Tclin Sodium-dependent dopamine transporter 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

SLC6A4 Tclin Sodium-dependent serotonin transporter 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

PGR Tclin Progesterone receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

PDE3A Tclin cGMP-inhibited 3',5'-cyclic phosphodiesterase A 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

PTGS1 Tclin Prostaglandin G/H synthase 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

PDE4A Tclin cAMP-specific 3',5'-cyclic phosphodiesterase 4A 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

LMNA Tbio Prelamin-A/C 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ABCC2 Tchem Canalicular multispecific organic anion transporter 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ABCC3 Tbio Canalicular multispecific organic anion transporter 2 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ABCC4 Tchem Multidrug resistance-associated protein 4 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

DRD3 Tclin D(3) dopamine receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CHRM2 Tclin Muscarinic acetylcholine receptor M2 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ACHE Tclin Acetylcholinesterase 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ABCB11 Tchem Bile salt export pump 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CHRM1 Tclin Muscarinic acetylcholine receptor M1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ADRA2A Tclin Alpha-2A adrenergic receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ADRA1A Tclin Alpha-1A adrenergic receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

AR Tclin Androgen receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

MAOA Tclin Amine oxidase [flavin-containing] A 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ADORA1 Tclin Adenosine receptor A1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

HTR1A Tclin 5-hydroxytryptamine receptor 1A 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

HTR2B Tclin 5-hydroxytryptamine receptor 2B 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

TBXA2R Tclin Thromboxane A2 receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

F2 Tclin Prothrombin 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

MAPT Tclin Microtubule-associated protein tau 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

OPRM1 Tclin Mu-type opioid receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

Names and Identifiers

IUPAC Name undec-10-enoic acid
INCHI InChI=1S/C11H20O2/c1-2-3-4-5-6-7-8-9-10-11(12)13/h2H,1,3-10H2,(H,12,13)
InChi Key FRPZMMHWLSIFAZ-UHFFFAOYSA-N
Canonical SMILES C=CCCCCCCCCC(=O)O
Isomeric SMILES C=CCCCCCCCCC(=O)O
WGK Germany 1
RTECS YQ2975000
PubChem CID 5634
Molecular Weight 184.28
Beilstein 1762631

Certificates

Certificate of Analysis(COA)

Enter Lot Number to search for COA:

To view the certificate results,please click on a Lot number.For Lot numbers from past orders,please use our order status section

14 results found

Lot NumberCertificate TypeDateItem
I2202917Certificate of AnalysisJun 04, 2024 U106484
I2202920Certificate of AnalysisJun 04, 2024 U106484
E1808156Certificate of AnalysisNov 16, 2023 U106484
B2020044Certificate of AnalysisSep 13, 2023 U106484
H2123090Certificate of AnalysisMay 12, 2023 U106484
E2324709Certificate of AnalysisApr 27, 2023 U106484
E2324722Certificate of AnalysisApr 27, 2023 U106484
E2324724Certificate of AnalysisApr 27, 2023 U106484
E2324728Certificate of AnalysisApr 27, 2023 U106484
E2324730Certificate of AnalysisApr 27, 2023 U106484
L1803206Certificate of AnalysisJul 11, 2022 U106484
B2218261Certificate of AnalysisJan 04, 2022 U106484
B2218263Certificate of AnalysisJan 04, 2022 U106484
B2218329Certificate of AnalysisJan 04, 2022 U106484

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Chemical and Physical Properties

SolubilitySlightly soluble in water, can be freely mixed with ethanol, chloroform, ether, volatile oil or fatty oil.
Freezing Point(°C)24 °C
Refractive Index1.449
Flash Point(°F)149 °C
Flash Point(°C)149°C
Boil Point(°C)137°C
Melt Point(°C)23-25°C

Safety and Hazards(GHS)

Pictogram(s) GHS07
Signal Warning
Hazard Statements

H315:Causes skin irritation

H319:Causes serious eye irritation

H335:May cause respiratory irritation

H412:Harmful to aquatic life with long lasting effects

Precautionary Statements

P261:Avoid breathing dust/fume/gas/mist/vapors/spray.

P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses if present and easy to do - continue rinsing.

P273:Avoid release to the environment.

P280:Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352:IF ON SKIN: wash with plenty of water.

P501:Dispose of contents/container to ...

P264:Wash hands [and …] thoroughly after handling.

P362+P364:Take off contaminated clothing and wash it before reuse.

WGK Germany 1
RTECS YQ2975000
Merck Index 9848

Related Documents

References

1. Xing-Cong Li,Melissa R Jacob,Shabana I Khan,M Khalid Ashfaq,K Suresh Babu,Ameeta K Agarwal,Hala N Elsohly,Susan P Manly,Alice M Clark.  (2008-05-07)  Potent in vitro antifungal activities of naturally occurring acetylenic acids..  Antimicrobial agents and chemotherapy,  52  ((7)): (2442-2448).  [PMID:18458131]
2. Rongling Yang,Xueming Liu,Zhiyi Chen,Chunying Yang,Yaosheng Lin,Siyuan Wang.  (2014-10-21)  Highly efficient and enzymatic regioselective undecylenoylation of gastrodin in 2-methyltetrahydrofuran-containing systems..  PloS one,  ((10)): (e110342-e110342).  [PMID:25329539]
3. Adi Tzur-Balter,Zohar Shatsberg,Margarita Beckerman,Ester Segal,Natalie Artzi.  (2015-02-12)  Mechanism of erosion of nanostructured porous silicon drug carriers in neoplastic tissues..  Nature communications,  (6208-6208).  [PMID:25670235]
4. Betar M Gallant, X Wendy Gu, David Z Chen, Julia R Greer, Nathan S Lewis,.  (2015-04-16)  Tailoring of interfacial mechanical shear strength by surface chemical modification of silicon microwires embedded in Nafion membranes..  ACS nano,  ((5)): ( 5143-5153 ).  [PMID:25872455]
5. Bin Guan,Hamidreza Siampour,Zhao Fan,Shun Wang,Xiang Yang Kong,Abdelmadjid Mesli,Jian Zhang,Yaping Dan.  (2015-08-01)  Nanoscale Nitrogen Doping in Silicon by Self-Assembled Monolayers..  Scientific reports,  (12641-12641).  [PMID:26227342]
6. Xin Wang,Mengqi Tu,Kai Yan,Penghui Li,Long Pang,Ying Gong,Qing Li,Ruiqing Liu,Zushun Xu,Haibo Xu,Paul K Chu.  (2015-10-21)  Trifunctional Polymeric Nanocomposites Incorporated with Fe₃O₄/Iodine-Containing Rare Earth Complex for Computed X-ray Tomography, Magnetic Resonance, and Optical Imaging..  ACS applied materials & interfaces,  ((44)): (24523-24532).  [PMID:26484385]
7. Terence Tieu,Marcin Wojnilowicz,Pie Huda,Kristofer J Thurecht,Helmut Thissen,Nicolas H Voelcker,Anna Cifuentes-Rius.  (2020-11-03)  Nanobody-displaying porous silicon nanoparticles for the co-delivery of siRNA and doxorubicin..  Biomaterials science,  ((1)): (133-147).  [PMID:33135714]
8. Ying-Dan Hu,Ye-Zhi Qin,Ning Li,Min-Hua Zong.  (2014-06-04)  Highly efficient enzymatic synthesis of an ascorbyl unstaturated fatty acid ester with ecofriendly biomass-derived 2-methyltetrahydrofuran as cosolvent..  Biotechnology progress,  30  ((5)): (1005-1011).  [PMID:24891225]
9. S N Aisyiyah Jenie,Beatriz Prieto-Simon,Nicolas H Voelcker.  (2015-07-24)  Development of L-lactate dehydrogenase biosensor based on porous silicon resonant microcavities as fluorescence enhancers..  Biosensors & bioelectronics,  74  (637-643).  [PMID:26201980]

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