3-fenilpropionaldehído - ≥95% , CAS No.104-53-0

CAS: 104-53-0 Cat. No.: P109695 Peso molecular: 134.18 Beilstein Registry Number: 1071910 Número EC: 203-211-8
Disponible para pedir
GRADE & PURITY ≥95%
Synonyms
AI3-01377 | NCGC00256683-01 | hydrocinnamaidehyde | BP-11455 | 3-Phenylpropan-1-al | Hydrocinnamic aldehyde | Phenylpropionaldehyde | AKOS000120255 | NSC9271 | NSC-9271 | P0217 | Benzenepropanal, 9CI | beta -phenylpropionaldehyde | Propionaidehyde, 3-phen
Storage
Conservar a 2-8°C,cargado con argón
Shipped In
Hielo húmedo
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
5g
P109695-5g
3

9,90US$

14,90US$
Guardar 5,00 US$ (33.56%)
25g
P109695-25g
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17,90US$

26,90US$
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100g
P109695-100g
2

70,90US$

106,90US$
Guardar 36,00 US$ (33.68%)
500g
P109695-500g
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196,90US$

295,90US$
Guardar 99,00 US$ (33.46%)
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Why this grade

≥95% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Conservar a 2-8°C,cargado con argón Ships Hielo húmedo 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 17 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

El hidrocinamaldehído es cinamaldehído hidrogenado por doble enlace C=C. Se ha sintetizado mediante la hidrogenación selectiva del doble enlace C=C del cinamaldehído por diversos métodos. El hidrocinamaldehído y el nitrometano sufren la reacción de Henry para formar nitroaldoles . Las posiciones C1 y C3 marcadas con 13C del hidrocinamaldehído se sometieron a espectrometría de masas y se dilucidó el patrón de fragmentación.

Specifications

Sinónimos
AI3-01377 | NCGC00256683-01 | hydrocinnamaidehyde | BP-11455 | 3-Phenylpropan-1-al | Hydrocinnamic aldehyde | Phenylpropionaldehyde | AKOS000120255 | NSC9271 | NSC-9271 | P0217 | Benzenepropanal, 9CI | beta -phenylpropionaldehyde | Propionaidehyde, 3-phen
Especificaciones y pureza
≥95%
Condiciones de almacenamiento de almacenamiento
Conservar a 2-8°C, cargado con argón
Enviado en
Hielo húmedo
Pureza
≥95%
Nombres e identificadores
Sonrisas canónicasC1=CC=C(C=C1)CCC=O
IUPAC Name3-phenylpropanal
InChIKeyYGCZTXZTJXYWCO-UHFFFAOYSA-N
INCHI1S/C9H10O/c10-8-4-7-9-5-2-1-3-6-9/h1-3,5-6,8H,4,7H2
Isómeros SMILES C1=CC=C(C=C1)CCC=O
WGK Alemania 2
RTECS MW4890000
Peso molecular 134.18
Beilstein 1071910
Reaxy-Rn 1071910
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1071910&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
SuperclassBenzenoids
ClaseBenzene and substituted derivatives
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentBenzene and substituted derivatives
Alternative Parents Alpha-hydrogen aldehydes  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Monocyclic benzene moiety - Alpha-hydrogen aldehyde - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aldehyde - Aromatic homomonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as benzene and substituted derivatives. These are aromatic compounds containing one monocyclic ring system consisting of benzene.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





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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.

19 results found

Lot NumberCertificate TypeFechaArticulo
G2417416Certificate of AnalysisApr 07, 2026 P109695
G2417038Certificate of AnalysisApr 07, 2026 P109695
A2607096Certificate of AnalysisJan 16, 2026 P109695
C2228043Certificate of AnalysisOct 13, 2025 P109695
C2228128Certificate of AnalysisOct 13, 2025 P109695
C2228162Certificate of AnalysisOct 13, 2025 P109695
J2310177Certificate of AnalysisJul 15, 2025 P109695
B2507191Certificate of AnalysisFeb 11, 2025 P109695
K2513048Certificate of AnalysisFeb 11, 2025 P109695
G2509054Certificate of AnalysisJul 23, 2024 P109695
G2417415Certificate of AnalysisApr 11, 2024 P109695
G2417417Certificate of AnalysisApr 11, 2024 P109695
G2417418Certificate of AnalysisApr 11, 2024 P109695
G2412238Certificate of AnalysisApr 11, 2024 P109695
C2228129Certificate of AnalysisJan 08, 2024 P109695
C2228111Certificate of AnalysisJan 08, 2024 P109695
H2106205Certificate of AnalysisMay 10, 2023 P109695
H2106206Certificate of AnalysisMay 10, 2023 P109695
H2106207Certificate of AnalysisMay 10, 2023 P109695

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Propiedades químicas y físicas
SolubilidadMiscible with chloroform, dichloromethane, ethyl acetate, alcohol and ether. Immiscible with water.
SensibilidadAir Sensitive;;Heat sensitive;
Índice de refracción1.52-1.525
Punto de inflamación (°F) 95℃
Punto de inflamación (°C) 95℃
Punto de ebullición (°C)224-226°C
Punto de fusión (°C)-42°C
Peso molecular134.170 g/mol
XLogP31.300
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count1
Rotatable Bond Count3
Exact Mass134.073 Da
Monoisotopic Mass134.073 Da
Topological Polar Surface Area17.100 Ų
Heavy Atom Count10
Formal Charge0
Complexity92.900
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Citations of This Product
Referencias
1. Yuhang Cai, Anping Yin, Jianxiang Zhang, Jiatai Wang, Xiaofei Qin, Yibo Yang, Gaolei Qin, Xiaodong Sun, Peng He, Yong Yang.  (2023)  Carbon-Coated Ni-Fe Nanocatalysts: Bridging the Gap in Cinnamaldehyde Hydrogenation Performance and Durability.  Catalysts,  13  (12): (1474).  [PMID:] [10.3390/catal13121474]
2. Fuping Tian, Xinchi Zhang, Yingying Sheng, Xiao Chen, Xiang Wang, Changhai Liang.  (2023)  Metal-organic framework-derived Co-C catalyst for the selective hydrogenation of cinnamaldehyde to cinnamic alcohol.  CHINESE JOURNAL OF CHEMICAL ENGINEERING,      [PMID:] [10.1016/j.cjche.2023.04.013]
3. Xingcong Zhang, Hao Zhang, Guanghui Guo, Qingdi Sun, Xiaohui He, Hongbing Ji.  (2023)  Phosphorus-Doped Carbon-Supported Rh Nanoparticles for the Hydroformylation of Styrene with High Regioselectivity.  INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH,      [PMID:] [10.1021/acs.iecr.2c04328]
4. Fang-Hui Liu, Cheng-Long Gao, Cui-Cui Zhang, Hong-Ze Gang, Bo-Zhong Mu, Shi-Zhong Yang.  (2022)  A new zwitterionic surfactant with high interfacial activity and high salt tolerance derived from methyl oleate through an eco-friendly aryl-introducing method.  JOURNAL OF SURFACTANTS AND DETERGENTS,  26  (2): (135-144).  [PMID:] [10.1002/jsde.12635]
5. Rong Zhang, Liancheng Wang, Jingzhao Ren, Changchen Hu, Baoliang Lv.  (2022)  Effect of boron nitride overlayers on Co@BNNSs/BN-Catalyzed aqueous phase selective hydrogenation of cinnamaldehyde.  JOURNAL OF COLLOID AND INTERFACE SCIENCE,      [PMID:36334490] [10.1016/j.jcis.2022.10.117]
6. Shuibo Wang, Chunzheng Wu, Hongbo Yu, Yuting Chu, Shiwei Wang, Tong Li, Hongfeng Yin.  (2022)  Tuning the catalytic performance of Pt/SiO2 catalysts by CoOx modification for selective hydrogenations of unsaturated carbonyl compounds.  APPLIED SURFACE SCIENCE,      [PMID:] [10.1016/j.apsusc.2022.154867]
7. Yangyang Zhou, Chen Chen, Qiling Li, Yanbo Liu, Ting Wei, Youzhen Liu, Zebing Zeng, Darren Bradshaw, Bing Zhang, Jia Huo.  (2022)  Precise control of selective hydrogenation of α,β-unsaturated aldehydes in water mediated by ammonia borane.  APPLIED CATALYSIS B-ENVIRONMENTAL,      [PMID:] [10.1016/j.apcatb.2022.121348]
8. Xiaoyao Ma, Kaixin Liu, Yiman Han, Yongping Bai, Fukui Shen, Mukuo Wang, Wei Wei, Jianfeng Qin, Erwei Hao, Xiaotao Hou, Yuanyuan Hou, Gang Bai.  (2022)  Cinnamaldehyde Regulates the Generation of γ-aminobutyric Acid to Exert Sedation via Irreversible Inhibition of ENO1 in the Cerebellar Granular Layer.  MOLECULAR NUTRITION & FOOD RESEARCH,  66  (11): (2100963).  [PMID:35332659] [10.1002/mnfr.202100963]
9. Tian Fuping, Zhang Mengjie, Zhang Xinchi, Chen Xiao, Wang Jinliang, Zhang Yifu, Meng Changgong, Liang Changhai.  (2022)  Porous carbon-encapsulated Ni nanocatalysts for selective catalytic hydrogenation of cinnamaldehyde to hydrocinnamaldehyde.  JOURNAL OF MATERIALS SCIENCE,  57  (5): (3168-3182).  [PMID:] [10.1007/s10853-021-06796-z]
10. Shenghui Zhou, Fanglin Dai, Chao Dang, Ming Wang, Detao Liu, Fachuang Lu, Haisong Qi.  (2019)  Scale-up biopolymer-chelated fabrication of cobalt nanoparticles encapsulated in N-enriched graphene shells for biofuel upgrade with formic acid.  GREEN CHEMISTRY,  21  (17): (4732-4747).  [PMID:] [10.1039/C9GC01720H]
11. Yangyi Wu, Lijun Fan, Yixiang Chen, Xianhong Zhang, Dong Chen, Wantai Yang.  (2025)  Branching Structured Poly(vinyl chloride-co-hydroxyethyl acrylate)-g-polycaprolactone as Nonmigratory Polymeric Plasticizers and Compatibilizers in Flexible PVC.  ACS Applied Polymer Materials,      [PMID:] [10.1021/acsapm.4c03603]
12. Bin Chen, Jun Hu, Zhihao Yu, Lin Zhu, Chunzheng Wu, Hongbo Yu.  (2025)  Improving the Activity and Selectivity of Ir/SiO2 for the Selective Hydrogenation of Unsaturated Carbonyl Compounds by SnO2 Promotion.  INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH,      [PMID:] [10.1021/acs.iecr.4c04318]
13. Xing Gao, Ying Ma, Yingying Ruan, Wenna Zhang, Shihao Zhang, Wenxue Xiong, Dong Tian, Shiliu Yang, Pei Fan, Yanhui Yang, Yihu Dai.  (2024)  Water-promoted selective hydrogenation of cinnamaldehyde over hydrotalcite-derived Co catalysts.  Molecular Catalysis,      [PMID:] [10.1016/j.mcat.2024.114096]
14. Zhang Tianhao, Tian Yuan, Zhang Chong, Yan Tingting, Yan Hanwen, Zhang Guoliang, Li Jie, Li Zengxi, Wang Gang, Li Chunshan, Zhang Suojiang.  (2025)  Electronically tailored metal-ion-chelation strategy promotes ionic liquid catalysis at near-ambient condition.  Nature Communications,  16  (1): (1-12).  [PMID:41022719] [10.1038/s41467-025-63630-9]
15. Liwei Wang, Yanfu Ma, Haitao Li, Wenhao Luo, Jian Liu.  (2024)  Screening support effect of Pt/MOx for selective hydrogenation of cinnamaldehyde.  JOURNAL OF CATALYSIS,      [PMID:] [10.1016/j.jcat.2024.115391]
16. Jialu Zhang, Yu Fu, Peng Chen, Bowen Liu, Cuiling Ren.  (2025)  New silicon nanoparticles for “turn-on” detection of salicylaldehyde in food based on ESIPT mechanism.  FOOD CHEMISTRY,      [PMID:40440837] [10.1016/j.foodchem.2025.144879]
17. Yifan Zhang, Jiaying Liu, Shiwei Wang, Zhihao Yu, Haojian Zhang, Dong Wang, Lin Zhu, Chunzheng Wu, Hongbo Yu.  (2025)  Enhanced Selective Hydrogenation of Acetophenone over KIT-6 Supported Pd-MO x (M = Fe, Co, Ni) Hybrid Nanostructures.  Catalysis Science & Technology,      [PMID:] [10.1039/D5CY01108F]
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