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Elaidic acid - analytical standard,≥99.0% (GC), high purity , CAS No.112-79-8

In stock
Item Number
E101311
Grouped product items
SKU Size
Availability
Price Qty
E101311-100mg
100mg
4
$85.90
E101311-500mg
500mg
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$411.90
E101311-1g
1g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$721.90
E101311-5g
5g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$3,227.90

Basic Description

Synonyms trans-Octadec-9-enoic acid | 4837010H8C | 9-elaidic acid | OLEIC-13C18 ACID | SR-01000946663-1 | (9E)-octadec-9-enoic acid | CHEBI:27997 | EN300-1697685 | trans-.delta.(sup 9)-Octadecenoic acid | 9-octadecenoicacid | AKOS000278123 | EINECS 217-977-6 | SCH
Specifications & Purity analytical standard, ≥99%(GC)
Storage Temp Store at -20°C,Argon charged
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Grade analytical standard
Product Description

Elaidic acid is the 9-trans isomer of oleic acid. It is a monounsaturated trans-fatty acid which can be found in partially hydrogenated cooking oils. In human platelets incubated with arachidonic acid, elaidic acid inhibits HHT and HETE formation while inducing prostaglandin and thromboxane synthesis.
A monounsaturated trans-fatty acid that inhibits HHT and HETE formation in platelets.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Lipids and lipid-like molecules
Class Fatty Acyls
Subclass Fatty acids and conjugates
Intermediate Tree Nodes Not available
Direct Parent Long-chain fatty acids
Alternative Parents Unsaturated fatty acids  Straight chain fatty acids  Monocarboxylic acids and derivatives  Carboxylic acids  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular Framework Aliphatic acyclic compounds
Substituents Long-chain fatty acid - Unsaturated fatty acid - Straight chain fatty acid - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound
Description This compound belongs to the class of organic compounds known as long-chain fatty acids. These are fatty acids with an aliphatic tail that contains between 13 and 21 carbon atoms.
External Descriptors Unsaturated fatty acids

Associated Targets(Human)

TOP1 Tclin DNA topoisomerase I (7553 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
FABP4 Tchem Fatty acid binding protein adipocyte (764 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CRABP2 Tchem Cellular retinoic acid-binding protein II (10 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
TERT Tchem Telomerase reverse transcriptase (2428 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

Mmp2 Matrix metalloproteinase-2 (12 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Pseudomonas aeruginosa (123386 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Staphylococcus aureus (210822 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Staphylococcus epidermidis (22802 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Escherichia coli (133304 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Enterococcus hirae (484 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

IUPAC Name (E)-octadec-9-enoic acid
INCHI InChI=1S/C18H34O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(19)20/h9-10H,2-8,11-17H2,1H3,(H,19,20)/b10-9+
InChIKey ZQPPMHVWECSIRJ-MDZDMXLPSA-N
Smiles CCCCCCCCC=CCCCCCCCC(=O)O
Isomeric SMILES CCCCCCCC/C=C/CCCCCCCC(=O)O
WGK Germany 1
RTECS JX6125000
UN Number 1206
Molecular Weight 282.46
Beilstein 1726543
Reaxy-Rn 1726541
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1726541&ln=

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.

6 results found

Lot Number Certificate Type Date Item
G2201276 Certificate of Analysis Apr 03, 2024 E101311
G2201275 Certificate of Analysis Apr 03, 2024 E101311
A2503291 Certificate of Analysis Apr 03, 2024 E101311
G2201278 Certificate of Analysis Apr 03, 2024 E101311
E2225281 Certificate of Analysis Feb 20, 2024 E101311
H2106044 Certificate of Analysis May 10, 2023 E101311

Chemical and Physical Properties

Solubility Soluble in water (<0.1 mg/ml at 25 °C), chloroform (50 mg/ml), DMSO (~100 mg/ml), DMF (~100 mg/ml), and ethanol.
Sensitivity heat sensitive, air sensitive
Flash Point(°F) >235.4 °F
Flash Point(°C) >113 °C
Boil Point(°C) 288 °C/100 mmHg
Melt Point(°C) 42-44°C
Molecular Weight 282.500 g/mol
XLogP3 6.500
Hydrogen Bond Donor Count 1
Hydrogen Bond Acceptor Count 2
Rotatable Bond Count 15
Exact Mass 282.256 Da
Monoisotopic Mass 282.256 Da
Topological Polar Surface Area 37.300 Ų
Heavy Atom Count 20
Formal Charge 0
Complexity 234.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 1
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 1
Covalently-Bonded Unit Count 1

Citations of This Product

1. Jing Lu, Ziheng Chen, Xiujuan Bu, Shanshan Chen, Shuang Guan.  (2023)  Elaidic acid induced hepatocyte pyroptosis via autophagy-CTSB-NLRP3 pathway.  FOOD AND CHEMICAL TOXICOLOGY,  181  (114060). 
2. Fei-Hua Wang, Xiao-Feng Guo, Yao-Cheng Fan, Hai-Bin Tang, Wei Liang, Hong Wang.  (2022)  Determination of trans-fatty acids in food samples based on the precolumn fluorescence derivatization by high performance liquid chromatography.  JOURNAL OF SEPARATION SCIENCE,  45  (8): (1425-1433). 
3. Tianli Guo, Hongrui Hou, Yufan Liu, Ling Chen, Bo Zheng.  (2021)  In vitro digestibility and structural control of rice starch-unsaturated fatty acid complexes by high-pressure homogenization.  CARBOHYDRATE POLYMERS,  256  (117607). 
4. Xiaochao Zhang, Jiabing Wei, Guangmin Ren, Changming Zhang, Zhanfeng Zheng, Caimei Fan.  (2019)  BiOBr-photocatalyzed cis–trans isomerization of 9-octadecenoic acids in different atmospheres.  Catalysis Science & Technology,  (13): (3380-3387). 
5. Feng Zhang, Xiaojie Wang, Xu Jie, Weili Wei.  (2018)  Test Paper for Colorimetric Inspection of Fatty Acids and Edible Oils.  SENSORS,  18  (10): (3252). 
6. Jingqing Wu, Ying Ge, Weidong Qin.  (2014)  Combination of Running-Buffer-Mediated Extraction and Polyamidoamine-Dendrimer-Assisted Capillary Electrophoresis for Rapid and Sensitive Determination of Free Fatty Acids in Edible Oils.  JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY,  62  (18): (4104–4111). 
7. Yibo Zhang, Yang Liu, Wei Wang, Chunlai Liu, Hongyu Zhou, Na Wang, Jianglei Hu, Fengwei Shi.  (2025)  Design of dual active site composites of HPW@MOF-199 embedded in SBA-15 functionalized with -COOH groups: Efficient catalysts for esterification reactions.  Molecular Catalysis,  573  (114824). 
8. Bin Wang, Kai Gao, Yujie Wang, Qiuying Chang, He Yang.  (2024)  Synergistic dispersion, adsorption, and anti-wear effects of magnesium silicate hydroxide nanomaterials and carboxylic acid.  APPLIED SURFACE SCIENCE,  665  (160373). 

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