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Behenic acid - technical,≥85%, high purity , CAS No.112-85-6

9 Citations
Item Number
B105674
Grouped product items
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B105674-25g
25g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$19.90
B105674-100g
100g
In stock
$22.90
B105674-250g
250g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$24.90
B105674-500g
500g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$43.90
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Carbonyl compound carboxylic acid

Basic Description

SynonymsB1248 | Hydrofol Acid 560 | 1219804-98-4 | A854667 | C08281 | 1193721-65-1 | Edenor C 22-85R | CH3-[CH2]20-COOH | H390488X0A | Dokosansaeure | DTXSID3026930 | HSDB 5578 | D0963 | n-Docosanoate | Behenic acid, 99% | CRODACID B | Behenic acid, analytical st
Specifications & Puritytechnical grade, ≥85%
Shipped InNormal
Gradetechnical grade
Product Description

Behenic acid is used to give hair conditioners and moisturizers their smoothing properties. It is also used to investigate the phase behavior of long-chain acids in supercritical propane.

Associated Targets(Human)

HDAC6 Tclin Histone deacetylase 6 (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)
BCHE Tclin Cholinesterase (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
PPARA Tclin Peroxisome proliferator-activated receptor alpha (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
PPARD Tchem Peroxisome proliferator-activated receptor delta (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
PPARG Tclin Peroxisome proliferator-activated receptor gamma (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
ACHE Tclin Acetylcholinesterase (18204 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PPARG Tclin Peroxisome proliferator-activated receptor gamma (15191 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PPARA Tclin Peroxisome proliferator-activated receptor alpha (9197 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Ppard Peroxisome proliferator-activated receptor delta (358 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Hdac6 Histone deacetylase 6 (222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Pseudomonas aeruginosa (123386 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Staphylococcus aureus (210822 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Escherichia coli (133304 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Bacillus subtilis (32866 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Candida albicans (78123 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
BCHE Cholinesterase (8742 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Names and Identifiers

IUPAC Name docosanoic acid
INCHI InChI=1S/C22H44O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22(23)24/h2-21H2,1H3,(H,23,24)
InChi Key UKMSUNONTOPOIO-UHFFFAOYSA-N
Canonical SMILES CCCCCCCCCCCCCCCCCCCCCC(=O)O
Isomeric SMILES CCCCCCCCCCCCCCCCCCCCCC(=O)O
PubChem CID 8215
Molecular Weight 340.58
Beilstein 1792887
Reaxy-Rn 1792887

Certificates

Certificate of Analysis(COA)

Enter Lot Number to search for COA:

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

4 results found

Lot NumberCertificate TypeDateItem
J2015160Certificate of AnalysisAug 16, 2024 B105674
C1621011Certificate of AnalysisOct 09, 2023 B105674
K1813247Certificate of AnalysisSep 15, 2022 B105674
F2328128Certificate of AnalysisSep 26, 2021 B105674

Chemical and Physical Properties

SolubilitySoluble in DMF (~3 mg/ml), hot methanol, water (0.15 mg/ml at 25°C), chloroform, and ethanol (2.18 mg/ml at 25°C).
Refractive Index1.427
Boil Point(°C)306°C/60mmHg
Melt Point(°C)72-80°C

Safety and Hazards(GHS)

Reaxy-Rn 1792887
Merck Index 1023

Related Documents

 SDS

 Specification Sheet

Citations of This Product

How to Cite Aladdin Scientific Products?
1. Wenjing Ma, Bin Yang, Hao Zhang, Dalong Sun.  (2023)  From emulsion to gel: Self-assembly behavior of ionic liquid surfactants in the water–oil interface.  JOURNAL OF MOLECULAR LIQUIDS,  390  (11): (123133).  [PMID:21123169] [10.1016/j.molliq.2023.123133]
2. Fengchang Huang, Xiaoming Mo, Xuesong Li, Maolan Peng, Yulu Zhou, Xiaoma Tao, Yifang Ouyang, Jialong Zhao.  (2022)  Improved efficiency for lead-free CsCu2I3 halide microplatelets by suppressing surface pinholes via surface functionalization.  JOURNAL OF LUMINESCENCE,  252  (119390).  [PMID:] [10.1016/j.jlumin.2022.119390]
3. Yujie Zhang, Hui Zhong, Shouyong Zhou, Haifeng Han, Mingliang Zhang, Hongdeng Qiu.  (2021)  A docosyl-terminated polyamine amphiphile-bonded stationary phase for multimodal separations in liquid chromatography.  JOURNAL OF CHROMATOGRAPHY A,  1642  (462045).  [PMID:33735643] [10.1016/j.chroma.2021.462045]
4. Yi Xia, Jie Shi, Qian Sun, Dan Wang, Xiao-Fei Zeng, Jie-Xin Wang, Jian-Feng Chen.  (2020)  Controllable synthesis and evolution mechanism of monodispersed Sub-10 nm ZrO2 nanocrystals.  CHEMICAL ENGINEERING JOURNAL,  394  (124843).  [PMID:] [10.1016/j.cej.2020.124843]
5. Qi Zhao, Jian Li, Yang Xu, Dandan Lv, Kanyasiri Rakariyatham, Dayong Zhou.  (2019)  Rapid extraction of free fatty acids from edible oil after accelerated storage based on amino-modified magnetic silica nanospheres.  Analytical Methods,  11  (35): (4520-4527).  [PMID:] [10.1039/C9AY01082C]
6. Chao Li, Kaixiang Zhou, Dongmei Chen, Wei Xu, Yanfei Tao, Yuanhu Pan, Kuiyu Meng, Muhammad Abu Bakr Shabbir, Qianying Liu, Lingli Huang, Shuyu Xie.  (2019)  Solid lipid nanoparticles with enteric coating for improving stability, palatability, and oral bioavailability of enrofloxacin.  International Journal of Nanomedicine,      [PMID:30880969] [10.2147/IJN.S183479]
7. Haifeng Han, Yujie Zhang, Renling Lu, Mingliang Zhang.  (2019)  An alternative approach for preparation of amide-embedded stationary phase for reversed-phase liquid chromatography.  JOURNAL OF CHROMATOGRAPHY A,  1593  (24).  [PMID:30712822] [10.1016/j.chroma.2019.01.054]
8. Yanfei Tao, Fei Yang, Kuiyu Meng, Dongmei Chen, Yujuan Yang, Kaixiang Zhou, Wanhe Luo, Wei Qu, Yuanhu Pan, Zonghui Yuan, Shuyu Xie.  (2019)  Exploitation of enrofloxacin-loaded docosanoic acid solid lipid nanoparticle suspension as oral and intramuscular sustained release formulations for pig.  DRUG DELIVERY,      [PMID:30880494] [10.1080/10717544.2019.1580798]
9. Yujie Zhang,Renling Lu,Ming Chen,Shouyong Zhou,Dabing Zhang,Haifeng Han,Mingliang Zhang,Hongdeng Qiu.  (2020-08-17)  A highly efficient acyl-transfer approach to urea-functionalized silanes and their immobilization onto silica gel as stationary phases for liquid chromatography..  Journal of chromatography. A,  1626  (461366-461366).  [PMID:32797845]

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