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10-Undecenal - 97%, high purity , CAS No.112-45-8

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10-Undecenal - 97%, high purity , CAS No.112-45-8

6 Citations

COA

Grade & Purity:

≥97%

Cas Number: 112-45-8
Molecular Weight: 168.28
EC Number: 203-973-1
MDL number: MFCD00007032
PubChem CID: 8187

In stock

Item Number

U114506

Grouped product items
SKU	Size	Availability	Price
U114506-5ml	5ml	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$10.90
U114506-25ml	25ml	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$39.90
U114506-100ml	100ml	1	$143.90
U114506-500ml	500ml	2	$646.90

View related series

aldehyde (388) Non heterocyclic block (8163)

Basic Description

Synonyms	CAS-112-45-8 \| FEMA No. 3095 \| EINECS 203-973-1 \| NCGC00255582-01 \| n-UNDECYLENIC ALDEHYDE (10-1) \| J-002781 \| BRN 1746480 \| CHEBI:125536 \| 4-01-00-03520 (Beilstein Handbook Reference) \| 10-Undecylenic aldehyde \| undec-10-en-1-al \| undecylenal \| 10-UNDECE
Specifications & Purity	≥97%
Storage Temp	Store at 2-8°C,Argon charged
Shipped In	Wet ice This product requires cold chain shipping. Ground and other economy services are not available.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organic oxygen compounds
  - Class Organooxygen compounds
    - Subclass Carbonyl compounds
      - Level5 Aldehydes
        Level6 Medium-chain aldehydes

Kingdom	Organic compounds
Superclass	Organic oxygen compounds
Class	Organooxygen compounds
Subclass	Carbonyl compounds
Intermediate Tree Nodes	Aldehydes
Direct Parent	Medium-chain aldehydes
Alternative Parents	Alpha-hydrogen aldehydes Organic oxides Hydrocarbon derivatives
Molecular Framework	Aliphatic acyclic compounds
Substituents	Medium-chain aldehyde - Alpha-hydrogen aldehyde - Organic oxide - Hydrocarbon derivative - Aliphatic acyclic compound
Description	This compound belongs to the class of organic compounds known as medium-chain aldehydes. These are an aldehyde with a chain length containing between 6 and 12 carbon atoms.
External Descriptors	Fatty aldehydes
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Names and Identifiers

IUPAC Name	undec-10-enal
INCHI	InChI=1S/C11H20O/c1-2-3-4-5-6-7-8-9-10-11-12/h2,11H,1,3-10H2
InChIKey	OFHHDSQXFXLTKC-UHFFFAOYSA-N
Smiles	C=CCCCCCCCCC=O
Isomeric SMILES	C=CCCCCCCCCC=O
WGK Germany	2
RTECS	YQ2835000
PubChem CID	8187
Molecular Weight	168.28
Reaxy-Rn	1746480

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
A2210115	Certificate of Analysis	Jul 09, 2025	U114506
A2210118	Certificate of Analysis	Jul 09, 2025	U114506
A2210116	Certificate of Analysis	Jul 09, 2025	U114506
A2210117	Certificate of Analysis	Jul 09, 2025	U114506
K1512061	Certificate of Analysis	Aug 07, 2023	U114506
D1917045	Certificate of Analysis	Nov 11, 2022	U114506

Chemical and Physical Properties

Solubility	Insoluble in water
Sensitivity	Air Sensitive,Heat Sensitive
Refractive Index	1.44
Flash Point(°F)	199.4 °F
Flash Point(°C)	100 °C
Boil Point(°C)	98-100 °C/3 mmHg (lit.)
Melt Point(°C)	7°C
Molecular Weight	168.280 g/mol
XLogP3	3.800
Hydrogen Bond Donor Count	0
Hydrogen Bond Acceptor Count	1
Rotatable Bond Count	9
Exact Mass	168.151 Da
Monoisotopic Mass	168.151 Da
Topological Polar Surface Area	17.100 Å²
Heavy Atom Count	12
Formal Charge	0
Complexity	108.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

Citations of This Product

How to Cite Aladdin Scientific Products?

1. Youyou Yang, Jing Li, Jiangtao Xing, Weihai Xing, Chaohua Tang, Zhenghua Rao, Junmin Zhang. (2022) Untargeted Profiling and Differentiation of Volatiles in Varieties of Meat Using GC Orbitrap MS. Foods, 11 (24): (3997).
2. Shi Yanqin, Chen Lukai, Ma Biao, Lu Songyan, Chen Si, He Huiwen, Ma Meng, Wang Xu. (2022) An oligomer of the bis-uracil derivative as an organic thermal stabilizer with a super low migration ratio for PVC. JOURNAL OF THERMAL ANALYSIS AND CALORIMETRY, 147 (23): (13351-13361).
3. Qing Wan, Ruming Jiang, Liucheng Mao, Dazhuang Xu, Guangjian Zeng, Yingge Shi, Fengjie Deng, Meiying Liu, Xiaoyong Zhang, Yen Wei. (2017) A powerful “one-pot” tool for fabrication of AIE-active luminescent organic nanoparticles through the combination of RAFT polymerization and multicomponent reactions. Materials Chemistry Frontiers, 1 (6): (1051-1058).
4. Yanheng He, Sanpeng Mao, Tianwei Zhang, Shangheng Zeng, Hao Duan, Ronghua Zhuang, Jianying Yu. (2024) Preparation and properties of self-healing SBS modified bitumen with dynamic acylhydrazone bonds. EUROPEAN POLYMER JOURNAL, 210 (112932).
5. Fang Wang, Xuchen Wang, Wenlong Xiao, Mengyao Zhu, Kai Huang, Nani Wang. (2024) Rapid and label-free quantitation of lipid peroxidation marker 4-hydroxy-2-nonenal using a localized surface plasmon resonance biosensor. MICROCHEMICAL JOURNAL, 207 (111682).
6. Youyou Yang, Dapeng Liu, Weihai Xing, Chaohua Tang, Xiaohui Feng, Junmin Zhang. (2024) Simulating fatty acid autoxidation and exploring the related volatiles formation mechanism. LWT-FOOD SCIENCE AND TECHNOLOGY, 214 (117083).

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