Elaidic acid - analytical standard, ≥99%(GC) , CAS No.112-79-8

CAS: 112-79-8 Cat. No.: E101311 Peso molecular: 282.46 Beilstein Registry Number: 1726543 Número EC: 204-006-6
Disponible para pedir
GRADE & PURITY Analytical standard ? Analytical standard — certified-purity material for quantitative calibration. Use to prepare calibration standards and validate analytical methods. ≥99%(GC)
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
Storage
Store at -20°C,Argon charged
Shipped In
Ice chest + Ice pads
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
100mg
E101311-100mg
4
39,90US$
500mg
E101311-500mg
3
119,90US$
1g
E101311-1g
3
199,90US$
5g
E101311-5g
1
829,90US$
Enter a quantity for the sizes you want to add.
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Why this grade

analytical standard, ≥99%(GC) Analytical standard for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at -20°C,Argon charged Ships Ice chest + Ice pads 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 9 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

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.

Specifications

Sinónimos
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
Especificaciones y pureza
analytical standard, ≥99%(GC)
Condiciones de almacenamiento de almacenamiento
Store at -20°C, Argon charged
Enviado en
Ice chest + Ice pads
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Grado
Analytical standard
Pureza
≥99%(GC)
Nombres e identificadores
Sonrisas canónicasCCCCCCCCC=CCCCCCCCC(=O)O
IUPAC Name(E)-octadec-9-enoic acid
InChIKeyZQPPMHVWECSIRJ-MDZDMXLPSA-N
INCHI1S/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+
Isómeros SMILES CCCCCCCC/C=C/CCCCCCCC(=O)O
WGK Alemania 1
RTECS JX6125000
Número ONU 1206
Peso molecular 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=

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
ClaseFatty Acyls
SubclassFatty acids and conjugates
Intermediate Tree Nodes Not available
Direct ParentLong-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 FrameworkAliphatic 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
DescripciónThis 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
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
TOP1 Tclin DNA topoisomerase I (7553 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
FABP4 Tchem Fatty acid binding protein adipocyte (764 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CRABP2 Tchem Cellular retinoic acid-binding protein II (10 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TERT Tchem Telomerase reverse transcriptase (2428 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
Mmp2 Matrix metalloproteinase-2 (12 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
Staphylococcus epidermidis (22802 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Escherichia coli (133304 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Enterococcus hirae (484 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
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 NumberCertificate TypeFechaArticulo
G2201275Certificate of AnalysisJan 19, 2026 E101311
G2201276Certificate of AnalysisJan 19, 2026 E101311
G2201278Certificate of AnalysisJan 19, 2026 E101311
E2225281Certificate of AnalysisOct 29, 2025 E101311
A2503291Certificate of AnalysisApr 03, 2024 E101311
H2106044Certificate of AnalysisMay 10, 2023 E101311
Propiedades químicas y físicas
SolubilidadSoluble in water (<0.1 mg/ml at 25 °C), chloroform (50 mg/ml), DMSO (~100 mg/ml), DMF (~100 mg/ml), and ethanol.
Sensibilidadheat sensitive, air sensitive
Punto de inflamación (°F)>235.4 °F
Punto de inflamación (°C)>113 °C
Punto de ebullición (°C)288 °C/100 mmHg
Punto de fusión (°C)42-44°C
Peso molecular282.500 g/mol
XLogP36.500
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count2
Rotatable Bond Count15
Exact Mass282.256 Da
Monoisotopic Mass282.256 Da
Topological Polar Surface Area37.300 Ų
Heavy Atom Count20
Formal Charge0
Complexity234.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count1
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds1
Covalently-Bonded Unit Count1
Preguntas frecuentes y artículos
Citations of This Product
Referencias
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,      [PMID:37748573] [10.1016/j.fct.2023.114060]
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).  [PMID:35112469] [10.1002/jssc.202100792]
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,      [PMID:33483084] [10.1016/j.carbpol.2020.117607]
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).  [PMID:] [10.1039/C9CY00339H]
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).  [PMID:30262762] [10.3390/s18103252]
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,      [PMID:24758299] [10.1021/jf4056105]
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,      [PMID:] [10.1016/j.mcat.2025.114824]
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,      [PMID:] [10.1016/j.apsusc.2024.160373]
9. Bo Zheng, Hui Wen, Xingwei Xiang, Bin Zheng.  (2026)  Hierarchical assembly and digestive resistance of starch-unsaturated fatty acid complexes regulated by ultrasound-assisted high-pressure microfluidization.  CARBOHYDRATE POLYMERS,      [PMID:] [10.1016/j.carbpol.2026.125153]
Calculadoras de soluciones
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