trans-3-Hydroxycinnamic acid - ≥99% , CAS No.14755-02-3

CAS: 14755-02-3 Cat. No.: H100569 Peso molecular: 164.16 Beilstein Registry Number: 2084229 Número EC: 604-589-0
Disponible para pedir
GRADE & PURITY ≥99%
Synonyms
Cinnamic acid, 3-hydroxy- | trans-3-Hydroxycinnamic acid, 99% | 3-(3-hydroxyphenyl)-2-propenoic acid | 3-(3-Hydroxyphenyl)acrylsaeure | bmse000093 | Q6712039 | (E)-3-(3-hydroxyphenyl)prop-2-enoic acid | LS-13594 | HY-113357 | (2E)-3-(3-hydroxyphenyl)prop-
Storage
Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
5g
H100569-5g
5
17,90US$
10g
H100569-10g
3
33,90US$
25g
H100569-25g
1
65,90US$
50g
H100569-50g
1
117,90US$
100g
H100569-100g
1
211,90US$
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥99% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

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 3 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinónimos
Cinnamic acid, 3-hydroxy- | trans-3-Hydroxycinnamic acid, 99% | 3-(3-hydroxyphenyl)-2-propenoic acid | 3-(3-Hydroxyphenyl)acrylsaeure | bmse000093 | Q6712039 | (E)-3-(3-hydroxyphenyl)prop-2-enoic acid | LS-13594 | HY-113357 | (2E)-3-(3-hydroxyphenyl)prop-
Especificaciones y pureza
≥99%
Condiciones de almacenamiento de almacenamiento
Room temperature
Enviado en
Normal
Pureza
≥99%
Nombres e identificadores
Pubchem Sid488190844
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488190844
Sonrisas canónicasC1=CC(=CC(=C1)O)C=CC(=O)O
IUPAC Name(E)-3-(3-hydroxyphenyl)prop-2-enoic acid
InChIKeyKKSDGJDHHZEWEP-SNAWJCMRSA-N
INCHI1S/C9H8O3/c10-8-3-1-2-7(6-8)4-5-9(11)12/h1-6,10H,(H,11,12)/b5-4+
Isómeros SMILES C1=CC(=CC(=C1)O)/C=C/C(=O)O
WGK Alemania 3
Peso molecular 164.16
Beilstein 2084229
Reaxy-Rn 2690254
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2690254&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
ClaseCinnamic acids and derivatives
SubclassHydroxycinnamic acids and derivatives
Intermediate Tree Nodes Not available
Direct ParentHydroxycinnamic acids
Alternative Parents Coumaric acids  Cinnamic acids  Styrenes  1-hydroxy-4-unsubstituted benzenoids  1-hydroxy-2-unsubstituted benzenoids  Monocarboxylic acids and derivatives  Carboxylic acids  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Cinnamic acid - Coumaric acid - Coumaric acid or derivatives - Hydroxycinnamic acid - Styrene - 1-hydroxy-4-unsubstituted benzenoid - 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
DescripciónThis 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 3-coumaric acid
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.

9 results found

Lot NumberCertificate TypeFechaArticulo
F2605094Certificate of AnalysisJun 15, 2026 H100569
A2608002Certificate of AnalysisJan 14, 2026 H100569
L2123160Certificate of AnalysisOct 11, 2025 H100569
L2123161Certificate of AnalysisOct 11, 2025 H100569
L2123162Certificate of AnalysisOct 11, 2025 H100569
L2123163Certificate of AnalysisOct 11, 2025 H100569
B1928086Certificate of AnalysisDec 12, 2022 H100569
D2415417Certificate of AnalysisDec 09, 2021 H100569
I2504083Certificate of AnalysisDec 09, 2021 H100569
Propiedades químicas y físicas
SolubilidadSoluble in ether, methanol, benzene, ethanol
Punto de fusión (°C)196°C
Peso molecular164.160 g/mol
XLogP31.800
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count3
Rotatable Bond Count2
Exact Mass164.047 Da
Monoisotopic Mass164.047 Da
Topological Polar Surface Area57.500 Ų
Heavy Atom Count12
Formal Charge0
Complexity186.000
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
Citations of This Product
Referencias
1. Li Min, Wang Yayao, Xiao Jianxing, Yan Xingfu, Liu Bingru.  (2023)  Allelopathic inhibition effects and mechanism of phenolic acids to Microcystis aeruginosa.  ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH,  30  (15): (45388-45397).  [PMID:36705822] [10.1007/s11356-022-24992-5]
2. Zhi-Ming Wu, Yu Cao, Jin-Han Guo, Xiu-Qin Fang, Cheng-Mei Liu.  (2022)  Bio-based poly(vinyl benzoxazine) derived from 3-hydroxycinnamic acid— An intrinsically green flame-retardant polymer free of both halogen and phosphorus.  REACTIVE & FUNCTIONAL POLYMERS,      [PMID:] [10.1016/j.reactfunctpolym.2022.105430]
3. Teng Sun, Haiping Zhang, Zhe Dong, Zengshe Liu, Mingming Zheng.  (2020)  Ultrasonic-promoted enzymatic preparation, identification and multi-active studies of nature-identical phenolic acid glycerol derivatives.  RSC Advances,  10  (19): (11139-11147).  [PMID:35495308] [10.1039/C9RA09830E]
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