p-Coumaric acid - Moligand™, ≥98% , CAS No.501-98-4

Name: p-Coumaric acid - Moligand™, ≥98% , CAS No.501-98-4
SKU: C108514
Availability: InStock

CAS: 501-98-4 Cat. No.: C108514 Fórmula: C₉H₈O₃ Peso molecular: 164.16 Beilstein Registry Number: 2207383 Número CE: 610-511-6

152 Citations COA

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p-Coumaric acid - Moligand™, ≥98% CAS No(501-98-4) by Aladdin Scientific

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Disponível para encomenda

GRADE & PURITY Moligand™ ? ≥98%

Synonyms

Storage

Room temperature,Argon charged

Shipped In

Normal

Specifications Nomes e identificadores Documentation Advanced Data Taxonomic Classification Estrutura 3D Alvos associados (humanos) Alvos associados (não humanos) Mecanismos de ação Certificados（CoA,COO,BSE/TSE e Mapa de Análise) Propriedades químicas e físicas FAQs e artigos Citations of This Product Calculadoras de soluções Revisões

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Why this grade

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

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Storage & shipping

Room temperature,Argon charged 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 152 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinónimos

Especificações e pureza

Moligand™, ≥98%

Mecanismos bioquímicos e fisiológicos

p-Coumaric acid is mainly a plant metabolite which exhibits antioxidant and anti-inflammatory properties It also shows bactericidal activity by damaging bacterial cell membrane and by interacting with bacterial DNA. In western blot, p-coumaric is also use

Condições de armazenamento de armazenamento

Room temperature,Argon charged

Enviado em

Normal

Grau

Moligand™

Pureza

≥98%

Nomes e identificadores

Pubchem Sid	488190845
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/488190845
Sorrisos canónicos	C1=CC(=CC=C1C=CC(=O)O)O
IUPAC Name	(E)-3-(4-hydroxyphenyl)prop-2-enoic acid
InChIKey	NGSWKAQJJWESNS-ZZXKWVIFSA-N
INCHI	1S/C9H8O3/c10-8-4-1-7(2-5-8)3-6-9(11)12/h1-6,10H,(H,11,12)/b6-3+
SMILES isoméricas	C1=CC(=CC=C1/C=C/C(=O)O)O
WGK Alemanha	2
RTECS	GD9095000
Peso molecular	164.16
Beilstein	2207383
Reaxy-Rn	2207381
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2207381&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

Kingdom Organic compounds
- Superclass Phenylpropanoids and polyketides
  - Classe Cinnamic acids and derivatives
    - Subclass Hydroxycinnamic acids and derivatives

Kingdom	Organic compounds
Superclass	Phenylpropanoids and polyketides
Classe	Cinnamic acids and derivatives
Subclass	Hydroxycinnamic acids and derivatives
Intermediate Tree Nodes	Not available
Direct Parent	Hydroxycinnamic acids
Alternative Parents	Coumaric acids Cinnamic acids Styrenes 1-hydroxy-2-unsubstituted benzenoids Monocarboxylic acids and derivatives Carboxylic acids Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework	Aromatic homomonocyclic compounds
Substituents	Cinnamic acid - Coumaric acid - Coumaric acid or derivatives - Hydroxycinnamic acid - Styrene - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Monocyclic benzene moiety - Benzenoid - Carboxylic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Organic oxide - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aromatic homomonocyclic compound
Descrição	This compound belongs to the class of organic compounds known as hydroxycinnamic acids. These are compounds containing an cinnamic acid where the benzene ring is hydroxylated.
External Descriptors	Paracoumaryl alcohol derivatives
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

Estrutura 3D

Alvos associados (humanos)

HCAR2 Tclin Hydroxycarboxylic acid receptor 2 (1 Activities)

Discover Target: HCAR2

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

CA2 Tclin Carbonic anhydrase 2 (1 Activities)

Discover Target: CA2

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

AKR1B1 Tclin Aldose reductase (1 Activities)

Discover Target: AKR1B1

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

EGFR Tclin Epidermal growth factor receptor erbB1 (33727 Activities)

Discover Target: EGFR

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

F2 Tclin Thrombin (11687 Activities)

Discover Target: F2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CA2 Tclin Carbonic anhydrase II (17698 Activities)

Discover Target: CA2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ESR1 Tclin Estrogen receptor alpha (17718 Activities)

Discover Target: ESR1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

TYR Tclin Tyrosinase (717 Activities)

Discover Target: TYR

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

PTGS2 Tclin Cyclooxygenase-2 (13999 Activities)

Discover Target: PTGS2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ESR2 Tclin Estrogen receptor beta (9272 Activities)

Discover Target: ESR2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

AKR1B1 Tclin Aldose reductase (1404 Activities)

Discover Target: AKR1B1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

PLA2G7 Tchem LDL-associated phospholipase A2 (1338 Activities)

Discover Target: PLA2G7

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CA3 Tclin Carbonic anhydrase III (753 Activities)

Discover Target: CA3

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CA6 Tclin Carbonic anhydrase VI (993 Activities)

Discover Target: CA6

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CA1 Tclin Carbonic anhydrase I (13240 Activities)

Discover Target: CA1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

SYK Tclin Tyrosine-protein kinase SYK (7372 Activities)

Discover Target: SYK

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CA5B Tclin Carbonic anhydrase VB (957 Activities)

Discover Target: CA5B

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CA5A Tclin Carbonic anhydrase VA (1168 Activities)

Discover Target: CA5A

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CA14 Tclin Carbonic anhydrase XIV (1305 Activities)

Discover Target: CA14

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CA12 Tclin Carbonic anhydrase XII (6231 Activities)

Discover Target: CA12

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CAMK2A Tchem CaM kinase II alpha (1938 Activities)

Discover Target: CAMK2A

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CA9 Tclin Carbonic anhydrase IX (8255 Activities)

Discover Target: CA9

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Caco-2 (12174 Activities)

Lot Number	Certificate Type	Data	Item
D2616012	Certificate of Analysis	Apr 27, 2026	C108514
D2608088	Certificate of Analysis	Apr 15, 2026	C108514
C2212529	Certificate of Analysis	Dec 10, 2025	C108514
B2223341	Certificate of Analysis	Dec 10, 2025	C108514
B2223348	Certificate of Analysis	Dec 10, 2025	C108514
B2625196	Certificate of Analysis	Jul 12, 2025	C108514
H2617038	Certificate of Analysis	Jul 12, 2025	C108514
H2511034	Certificate of Analysis	Jul 12, 2025	C108514
G2503047	Certificate of Analysis	Jul 12, 2025	C108514
H2121248	Certificate of Analysis	Jun 09, 2025	C108514
L2405541	Certificate of Analysis	Jun 26, 2024	C108514
L2405540	Certificate of Analysis	Jun 26, 2024	C108514
B2514013	Certificate of Analysis	Jun 26, 2024	C108514
L2405542	Certificate of Analysis	Jun 26, 2024	C108514
L2423557	Certificate of Analysis	Jun 26, 2024	C108514
F2518065	Certificate of Analysis	Jan 02, 2023	C108514
C2307649	Certificate of Analysis	Jan 02, 2023	C108514
C2307651	Certificate of Analysis	Jan 02, 2023	C108514
C2307646	Certificate of Analysis	Jan 02, 2023	C108514
C2307644	Certificate of Analysis	Jan 02, 2023	C108514
C2307630	Certificate of Analysis	Jan 02, 2023	C108514
C2307582	Certificate of Analysis	Jan 02, 2023	C108514
C2307580	Certificate of Analysis	Jan 02, 2023	C108514
C2307561	Certificate of Analysis	Jan 02, 2023	C108514
C2307559	Certificate of Analysis	Jan 02, 2023	C108514
D2407069	Certificate of Analysis	Jan 10, 2022	C108514
H2401052	Certificate of Analysis	Jan 10, 2022	C108514
L22151180	Certificate of Analysis	Jan 10, 2022	C108514
B2223373	Certificate of Analysis	Jan 10, 2022	C108514
B2223371	Certificate of Analysis	Jan 10, 2022	C108514
B2223370	Certificate of Analysis	Jan 10, 2022	C108514
B2223347	Certificate of Analysis	Jan 10, 2022	C108514
H2121244	Certificate of Analysis	Jul 02, 2021	C108514

Solubilidade	Solubility in Methanol very faint turbidity,Slightly soluble in water
Sensibilidade	air sensitive
Ponto de fusão (°C)	210-214°C
Peso molecular	164.160 g/mol
XLogP3	1.500
Hydrogen Bond Donor Count	2
Hydrogen Bond Acceptor Count	3
Rotatable Bond Count	2
Exact Mass	164.047 Da
Monoisotopic Mass	164.047 Da
Topological Polar Surface Area	57.500 Å²
Heavy Atom Count	12
Formal Charge	0
Complexity	178.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	1
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	1
Covalently-Bonded Unit Count	1

p-Coumaric acid - Moligand™, ≥98% , CAS No.501-98-4

Storage & shipping

Quality documents

Literature proof

Specifications

Documentation

📋 Safety Data Sheet (SDS)

✅ Certificate of Analysis (COA)

📊 Datasheet

🔬 Specification Sheet

Advanced Data

Molarity Calculator

Dilution Calculator

Reconstitution Calculator

Avaliações dos Clientes

📚 Citations by Application

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