Chnnamyl alcohol - ≥98% , CAS No.104-54-1

CAS: 104-54-1 Cat. No.: C110605 Peso molecular: 134.18 Beilstein Registry Number: 1903999 Número EC: 203-212-3
Disponible para pedir
GRADE & PURITY ≥98%
Synonyms
3-HYDROXY-1-PHENYLPROP-1-ENE | 3-PHENYL-2-PROPEN-1-OL | DTXSID9041491 | SR-01000944721-1 | Cinnamyl alcohol, 98% | HSDB 5011 | Cinnamyl alcohol, analytical standard | Tox21_300847 | GTPL12661 | (2E)-3-Phenyl-2-propen-1-ol | BBL027413 | BS-14235 | J-700106
Storage
Protected from light,Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
25g
C110605-25g
2
9,90US$
100g
C110605-100g
2

14,90US$

21,90US$
Guardar 7,00 US$ (31.96%)
250g
C110605-250g
4

25,90US$

47,90US$
Guardar 22,00 US$ (45.93%)
Enter a quantity for the sizes you want to add.
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Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Protected from light,Room temperature Ships Normal Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 25 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

Cinnamyl alcohol causes Friedel Crafts alkylation of bulky aromatic compound 2,4-di-tert-butylphenol using mesoporous aluminosilicate as catalyst. Cinnamyl alcohol undergoes partial oxidation in air to form cinnamaldehyde over a series of Bi-Pt/alumina catalysts. Cinnamyl alcohol is used in perfumery and in deodorant compositions.
Cinnamyl alcohol was used to study the alkylation of 2,4-di-tert-butylphenol by cinnamyl alcohol using aluminum-containing mesoporous ethane-silica catalyst. It was used to study gold nanoparticles supported on titanium dioxide catalysed oxidative coupling of alcohols and amines to form the corresponding imines.

Specifications

Sinónimos
3-HYDROXY-1-PHENYLPROP-1-ENE | 3-PHENYL-2-PROPEN-1-OL | DTXSID9041491 | SR-01000944721-1 | Cinnamyl alcohol, 98% | HSDB 5011 | Cinnamyl alcohol, analytical standard | Tox21_300847 | GTPL12661 | (2E)-3-Phenyl-2-propen-1-ol | BBL027413 | BS-14235 | J-700106
Especificaciones y pureza
≥98%
Condiciones de almacenamiento de almacenamiento
Protected from light, Room temperature
Enviado en
Normal
Pureza
≥98%
Nombres e identificadores
Pubchem Sid488195330
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488195330
Sonrisas canónicasC1=CC=C(C=C1)C=CCO
IUPAC Name(E)-3-phenylprop-2-en-1-ol
InChIKeyOOCCDEMITAIZTP-QPJJXVBHSA-N
INCHI1S/C9H10O/c10-8-4-7-9-5-2-1-3-6-9/h1-7,10H,8H2/b7-4+
Isómeros SMILES C1=CC=C(C=C1)/C=C/CO
WGK Alemania 2
RTECS GE2200000
CAS alternativo 4407-36-7
Número ONU 1987
Peso molecular 134.18
Beilstein 1903999
Reaxy-Rn 1903999
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1903999&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
SuperclassPhenylpropanoids and polyketides
ClaseCinnamyl alcohols
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentCinnamyl alcohols
Alternative Parents Styrenes  Primary alcohols  Hydrocarbon derivatives  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Cinnamyl alcohol - Styrene - Benzenoid - Monocyclic benzene moiety - Organic oxygen compound - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Alcohol - Aromatic homomonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as cinnamyl alcohols. These are aromatic alcohols containing a 3-phenylprop-2-en-1-ol moiety.
External Descriptors cinnamyl alcohol
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
TYR Tclin Tyrosinase (717 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
XDH Tclin Xanthine dehydrogenase (1038 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
UGT1A9 Tbio UDP-glucuronosyltransferase 1-9 (343 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
UGT2A1 UDP-glucuronosyltransferase 2A1 (59 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
Hrh4 Histamine H4 receptor (388 Activities)
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Pseudomonas aeruginosa (123386 Activities)
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Burkholderia cepacia (649 Activities)
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Enterobacter cloacae (7976 Activities)
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Klebsiella pneumoniae (43867 Activities)
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Micrococcus luteus (7463 Activities)
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Staphylococcus aureus (210822 Activities)
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Escherichia coli (133304 Activities)
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Aspergillus niger (16508 Activities)
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Bacillus subtilis (32866 Activities)
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Pichia kudriavzevii (7448 Activities)
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Candida albicans (78123 Activities)
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Trichophyton rubrum (3646 Activities)
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Mus musculus (284745 Activities)
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Rattus norvegicus (775804 Activities)
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RAW264.7 (28094 Activities)
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Trpa1 Transient receptor potential cation channel subfamily A member 1 (1003 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Abutilon theophrasti (831 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Aspergillus parasiticus (296 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Bursaphelenchus xylophilus (372 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Aspergillus sydowii (55 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.

20 results found

Lot NumberCertificate TypeFechaArticulo
F2225113Certificate of AnalysisApr 02, 2026 C110605
F2225157Certificate of AnalysisApr 02, 2026 C110605
F2225159Certificate of AnalysisApr 02, 2026 C110605
L2125023Certificate of AnalysisOct 11, 2025 C110605
L2125022Certificate of AnalysisOct 11, 2025 C110605
L2125021Certificate of AnalysisOct 11, 2025 C110605
L2001146Certificate of AnalysisSep 05, 2024 C110605
L2001145Certificate of AnalysisSep 05, 2024 C110605
C2510072Certificate of AnalysisJul 27, 2024 C110605
C2510073Certificate of AnalysisJul 27, 2024 C110605
C2510074Certificate of AnalysisJul 27, 2024 C110605
C2510075Certificate of AnalysisJul 27, 2024 C110605
E2613007Certificate of AnalysisJul 27, 2024 C110605
G2410586Certificate of AnalysisMay 09, 2024 C110605
G2410587Certificate of AnalysisMay 09, 2024 C110605
J1916160Certificate of AnalysisAug 08, 2023 C110605
H1905196Certificate of AnalysisMay 08, 2023 C110605
I2503087Certificate of AnalysisJun 08, 2022 C110605
B2307099Certificate of AnalysisJun 08, 2022 C110605
B2625156Certificate of AnalysisJun 08, 2022 C110605

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Propiedades químicas y físicas
SolubilidadSoluble in water 1.8 g/L (20°C).
SensibilidadLight sensitive.
Punto de congelación (°C)31 °C
Punto de inflamación (°F)126°
Punto de inflamación (°C)126°
Punto de ebullición (°C)249-250°C
Punto de fusión (°C)31-35°C
Peso molecular134.170 g/mol
XLogP31.900
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count1
Rotatable Bond Count2
Exact Mass134.073 Da
Monoisotopic Mass134.073 Da
Topological Polar Surface Area20.200 Ų
Heavy Atom Count10
Formal Charge0
Complexity101.000
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. 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. An Zhidong, Yang Piaoping, Duan Delong, Li Jiang, Wan Tong, Kong Yue, Caratzoulas Stavros, Xiang Shuting, Liu Jiaxing, Huang Lei, Frenkel Anatoly I., Jiang Yuan-Ye, Long Ran, Li Zhenxing, Vlachos Dionisios G..  (2023)  Highly active, ultra-low loading single-atom iron catalysts for catalytic transfer hydrogenation.  Nature Communications,  14  (1): (1-12).  [PMID:37863924] [10.1038/s41467-023-42337-9]
3. 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]
4. Shurui Xu, Baoqiang Lin, Qihang Huang, Wenting Qiu, Wenqian Yuan, Weirui Xu, Xingfeng Xue, Guoyu Zhong, Wenbo Liao, Wenlong Wang, Xiaobo Fu.  (2022)  Enhanced activity of alcohol oxidation on nitrogen-doped carbon by FeN interaction.  DIAMOND AND RELATED MATERIALS,      [PMID:] [10.1016/j.diamond.2022.109635]
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. Qianqian Zhang, Yifan Sun, Wei Li, Jinli Zhang, Yan Fu.  (2022)  Highly selective electrocatalytic hydrogenation of cinnamaldehyde over tin dioxide-supported palladium nanocatalysts.  INTERNATIONAL JOURNAL OF HYDROGEN ENERGY,      [PMID:] [10.1016/j.ijhydene.2022.09.004]
7. Yanghuan Huang, Haocheng Zhang, Lou Gao, Tianlan Yan, Yueer Yan, Yahong Zhang, Yi Tang.  (2022)  Direct grafting synthesis of bi-functional Zr–Al-MWW zeolites and their catalytic characteristics in Lewis-Brønsted cascade reaction.  MICROPOROUS AND MESOPOROUS MATERIALS,      [PMID:] [10.1016/j.micromeso.2022.112110]
8. 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]
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. Jinshan Song, Nengwei Ma, Wenqing Chen, Jianmeng Chen, Qizhou Dai.  (2021)  Insights into mechanism of catalytic ozonation of cinnamyl alcohol over core–shell Fe3O4@SiO2@La2O3 catalyst.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2021.119969]
11. Xiaoping Liu, Yunbo Zhai, Guangli Liu, Xiangmin Liu, Bei Wang, Zhexian Wang, Ya Zhu, Yuwei Fan, Haoran Shi, Min Xu.  (2021)  Mechanistic insights into enhanced waste activated sludge dewaterability with Cu(II) and Cu(II)/H2O2 treatment: Radical and non-radical pathway.  CHEMOSPHERE,      [PMID:34653483] [10.1016/j.chemosphere.2021.132549]
12. Liu Chen, Long Huali, Wu Xingdong, Hou Jinjun, Gao Lei, Yao Shuai, Lei Min, Zhang Zijia, Guo De-an, Wu Wanying.  (2021)  Quantitative and fingerprint analysis of proanthocyanidins and phenylpropanoids in Cinnamomum verum bark, Cinnamomum cassia bark, and Cassia twig by UPLC combined with chemometrics.  EUROPEAN FOOD RESEARCH AND TECHNOLOGY,  247  (11): (2687-2698).  [PMID:] [10.1007/s00217-021-03795-x]
13. Yunchang Fan, Hui Luo, Chunyan Zhu, Wenjin Li, Di Wu, Hongwei Wu.  (2021)  Hydrophobic natural alcohols based deep eutectic solvents: Effective solvents for the extraction of quinine.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2021.119112]
14. Hongbo Yu, Jihao Zhao, Chunzheng Wu, Bo Yan, Shuangliang Zhao, Hongfeng Yin, Shenghu Zhou.  (2021)  Highly Efficient Ir–CoOx Hybrid Nanostructures for the Selective Hydrogenation of Furfural to Furfuryl Alcohol.  LANGMUIR,      [PMID:33492955] [10.1021/acs.langmuir.0c03367]
15. Tao Guo, Ting Xu, Wentao Xia, Andrew J. Carrier, Li Wang, Xu Zhang.  (2020)  Graphene oxide and CuO double quantum dot composites (GOQD-q-CuO) with enhanced haloperoxidase-like activity and its application in colorimetric detection of H2O2 and glucose.  MATERIALS CHEMISTRY AND PHYSICS,      [PMID:] [10.1016/j.matchemphys.2020.124126]
16. Yingpeng Huo, Jiwen Hu, Yuanyuan Tu, Zhenzhu Huang, Shudong Lin, Yangfei Hu, Chao Feng.  (2020)  Platinum-Imidazolyl Schiff Base Complexes Immobilized in Periodic Mesoporous Organosilica Frameworks as Catalysts for Hydrosilylation.  APPLIED ORGANOMETALLIC CHEMISTRY,  34  (8): (e5697).  [PMID:] [10.1002/aoc.5697]
17. Fei Li, Yong Wang, Jian Du, Yong Zhu, Congying Xu, Licheng Sun.  (2017)  Simultaneous oxidation of alcohols and hydrogen evolution in a hybrid system under visible light irradiation.  APPLIED CATALYSIS B-ENVIRONMENTAL,      [PMID:] [10.1016/j.apcatb.2017.11.072]
18. Zhen Gao, Jianlin Chu, Tianyue Jiang, Tingting Xu, Bin Wu, Bingfang He.  (2017)  Lipase immobilization on functionalized mesoporous TiO2: Specific adsorption, hyperactivation and application in cinnamyl acetate synthesis.  PROCESS BIOCHEMISTRY,      [PMID:] [10.1016/j.procbio.2017.09.011]
19. Tao Wang, Pengfei Zhang, Yan Sun, Bing Liu, Yunling Liu, Zhen-An Qiao, Qisheng Huo, Sheng Dai.  (2017)  New Polymer Colloidal and Carbon Nanospheres: Stabilizing Ultrasmall Metal Nanoparticles for Solvent-Free Catalysis.  CHEMISTRY OF MATERIALS,      [PMID:] [10.1021/acs.chemmater.7b00710]
20. Lyu Fei, Gao Fei, Wei Qianqian, Liu Lin.  (2017)  Changes of membrane fatty acids and proteins of Shewanella putrefaciens treated with cinnamon oil and gamma irradiation.  Bioresources and Bioprocessing,  (1): (1-10).  [PMID:28203517] [10.1186/s40643-017-0140-1]
21. Fan Wang, Zehui Zhang.  (2016)  Catalytic Transfer Hydrogenation of Furfural into Furfuryl Alcohol over Magnetic γ-Fe2O3@HAP Catalyst.  ACS Sustainable Chemistry & Engineering,      [PMID:] [10.1021/acssuschemeng.6b02272]
22. Shaojie Liu, Huali Wang, Xiaomeng Chu.  (2016)  Nitroxide polymer brushes as efficient and recoverable catalysts for the selective oxidation of primary alcohols to aldehydes.  JOURNAL OF APPLIED POLYMER SCIENCE,  134  (1):   [PMID:] [10.1002/app.44365]
23. Zhang Guofu, Zhang Guihua, Lei Jie, Li Shasha, Xu Shengjun, Ding Chengrong, Shan Shang.  (2016)  Aerobic alcohol ammoxidation catalyzed by copper(I)/amino acid: a scalable protocol to nitriles.  CHEMICAL RESEARCH IN CHINESE UNIVERSITIES,  32  (4): (586-593).  [PMID:] [10.1007/s40242-016-6067-9]
24. Xiaoxue Wu, Jiao He, Huarong Xu, Kaishun Bi, Qing Li.  (2014)  Quality assessment of Cinnamomi Ramulus by the simultaneous analysis of multiple active components using high-performance thin-layer chromatography and high-performance liquid chromatography.  JOURNAL OF SEPARATION SCIENCE,  37  (18): (2490-2498).  [PMID:24964287] [10.1002/jssc.201400494]
25. Qingshan Zhao, Yang Li, Ru Liu, Ao Chen, Guoliang Zhang, Fengbao Zhang, Xiaobin Fan.  (2013)  Enhanced hydrogenation of olefins and ketones with a ruthenium complex covalently anchored on graphene oxide.  Journal of Materials Chemistry A,  (47): (15039-15045).  [PMID:] [10.1039/C3TA13378H]
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