Cuminaldehyde - ≥97% , CAS No.122-03-2

CAS: 122-03-2 Cat. No.: C117706 Peso molecular: 148.2 Beilstein Registry Number: 636547 Número EC: 204-516-9
Disponible para pedir
GRADE & PURITY ≥97%
Synonyms
cuminic aldehyde | p-cumic aldehyde | WLN: VHR DY1 & 1 | cuminal | EC 204-516-9 | HY-Y0790 | bmse000508 | cuminaldehyde | P-ISOPROPYLBENZALDEHYDE | p-iso-Propylbenzaldehyde | p-isopropyl-Benzaldehyde | Cumin aldehyde | p-(1-methylethyl)benzaldehyde | CHEB
Storage
Argon charged,Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
25g
C117706-25g
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.

14,90US$

22,90US$
Guardar 8,00 US$ (34.93%)
100g
C117706-100g
2

29,90US$

44,90US$
Guardar 15,00 US$ (33.41%)
500g
C117706-500g
1

74,90US$

112,90US$
Guardar 38,00 US$ (33.66%)
Enter a quantity for the sizes you want to add.
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Why this grade

≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Argon charged,Room temperature Ships Normal 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 7 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

Cuminaldehyde increases the insulin secretion in streptozotocin-induced diabetic rats. It suppresses melanin formation in cultured murine B16-F10 melanoma cells.
Cuminaldehyde has been used to study larvicidal and adulticidal toxicity of monoterpenes against Culex pipiens. It has been used in evaluation of chemical composition, antimicrobial and antioxidant activities of essential oil and various extracts of Eucalyptus gilii.

Specifications

Sinónimos
cuminic aldehyde | p-cumic aldehyde | WLN: VHR DY1 & 1 | cuminal | EC 204-516-9 | HY-Y0790 | bmse000508 | cuminaldehyde | P-ISOPROPYLBENZALDEHYDE | p-iso-Propylbenzaldehyde | p-isopropyl-Benzaldehyde | Cumin aldehyde | p-(1-methylethyl)benzaldehyde | CHEB
Especificaciones y pureza
≥97%
Condiciones de almacenamiento de almacenamiento
Argon charged, Room temperature
Enviado en
Normal
Pureza
≥97%
Nombres e identificadores
Pubchem Sid504750377
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504750377
Sonrisas canónicasCC(C)C1=CC=C(C=C1)C=O
IUPAC Name4-propan-2-ylbenzaldehyde
InChIKeyWTWBUQJHJGUZCY-UHFFFAOYSA-N
INCHI1S/C10H12O/c1-8(2)10-5-3-9(7-11)4-6-10/h3-8H,1-2H3
Isómeros SMILES CC(C)C1=CC=C(C=C1)C=O
WGK Alemania 2
RTECS CU7000000
Peso molecular 148.2
Beilstein 636547
Reaxy-Rn 636547
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=636547&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
ClasePrenol lipids
SubclassMonoterpenoids
Intermediate Tree Nodes Not available
Direct ParentAromatic monoterpenoids
Alternative Parents Monocyclic monoterpenoids  Phenylpropanes  Cumenes  Benzoyl derivatives  Benzaldehydes  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents P-cymene - Aromatic monoterpenoid - Monocyclic monoterpenoid - Cumene - Phenylpropane - Benzaldehyde - Benzoyl - Aryl-aldehyde - Benzenoid - Monocyclic benzene moiety - Hydrocarbon derivative - Aldehyde - Organic oxide - Organic oxygen compound - Organooxygen compound - Aromatic homomonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as aromatic monoterpenoids. These are monoterpenoids containing at least one aromatic ring.
External Descriptors a small molecule
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
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Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
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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.

10 results found

Lot NumberCertificate TypeFechaArticulo
I2510066Certificate of AnalysisSep 12, 2025 C117706
I2523068Certificate of AnalysisSep 12, 2025 C117706
C2222473Certificate of AnalysisSep 08, 2025 C117706
C2222482Certificate of AnalysisSep 08, 2025 C117706
C2222528Certificate of AnalysisSep 08, 2025 C117706
C2222618Certificate of AnalysisSep 08, 2025 C117706
G2313231Certificate of AnalysisApr 02, 2025 C117706
I2118058Certificate of AnalysisJun 15, 2023 C117706
A2105158Certificate of AnalysisOct 20, 2022 C117706
G1930213Certificate of AnalysisApr 14, 2022 C117706
Propiedades químicas y físicas
Sensibilidadair sensitive
Índice de refracción1.529-1.532
Punto de inflamación (°F)199.4 °F
Punto de inflamación (°C)93℃
Punto de ebullición (°C)234-235°C
Peso molecular148.200 g/mol
XLogP32.700
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count1
Rotatable Bond Count2
Exact Mass148.089 Da
Monoisotopic Mass148.089 Da
Topological Polar Surface Area17.100 Ų
Heavy Atom Count11
Formal Charge0
Complexity121.000
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. Hui Li, Keren Agyekumwaa Addo, Yi-gang Yu, Xing-long Xiao.  (2023)  Cuminaldehyde inhibits biofilm formation by affecting the primary adhesion of Staphylococcus aureus.  SOUTH AFRICAN JOURNAL OF BOTANY,      [PMID:] [10.1016/j.sajb.2023.02.031]
2. Zuobing Xiao, Chengjing Wu, Xinyu Lu, Yunwei Niu, Peiran Yu, Xiaojie Ma.  (2023)  Substituent effect on controlled release of fragrant aldehydes from pH-triggered nicotinoylhydrazone-based precursors.  Molecular Systems Design & Engineering,  (6): (767-774).  [PMID:] [10.1039/D2ME00279E]
3. Xu Zhang, Li-Hua Hu, Da-Wei Song, Yang Hu, Jiong Chen.  (2022)  Evaluation on prevention and treatment of cuminaldehyde in culture of shrimp against white spot syndrome virus.  AQUACULTURE,      [PMID:] [10.1016/j.aquaculture.2022.738760]
4. Changyue Deng, Chuan Cao, Yingying Zhang, Jingwei Hu, Yongqiang Gong, Mingming Zheng, Yibin Zhou.  (2021)  Formation and stabilization mechanism of β-cyclodextrin inclusion complex with C10 aroma molecules.  FOOD HYDROCOLLOIDS,      [PMID:] [10.1016/j.foodhyd.2021.107013]
5. Chenghui Zhang, Changzhu Li, Tariq Aziz, Metab Alharbi, Haiying Cui, Lin Lin.  (2024)  Screening of E. coli O157:H7 AI-2 QS inhibitors and their inhibitory effect on biofilm formation in combination with disinfectants.  Food Bioscience,      [PMID:] [10.1016/j.fbio.2024.103821]
6. Liu Dazhao, Reymick Okwong Oketch, Luo Yuwei, Chen Xin, Che JinXin, Tao Nengguo.  (2025)  Cuminaldehyde: a potent antifungal agent for managing postharvest blue mold disease in Citrus reticulata Blanco cv. Ponkan.  WORLD JOURNAL OF MICROBIOLOGY & BIOTECHNOLOGY,  41  (5): (1-11).  [PMID:40289242] [10.1007/s11274-025-04367-x]
7. Yao Wang, Junhua Qiu, Chengwei Wang, Ruiyu Yang, Fuyou Guo, Tian Li, Shili Li, Lei Yang, Wei Ding.  (2026)  Sustainable Strategy of Natural trans-Anethole in Controlling Bacterial Wilt: Virulence Suppression and Beneficial Microbiome Enrichment.  JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY,      [PMID:41568748] [10.1021/acs.jafc.5c13627]
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