4-Pyridinecarboxaldehyde - ≥98% , CAS No.872-85-5

CAS: 872-85-5 Cat. No.: P105913 Peso molecular: 107.11 Beilstein Registry Number: 105342 Número EC: 212-832-3
Disponible para pedir
GRADE & PURITY ≥98%
Synonyms
4-pyridincarboxaldehyde | EC 212-832-3 | 4-pyrdinecarboxaldehyde | 4-pyridinecarbox-aldehyde | 4-pyridine carbaldehyde | 4-Pyridinecarboxaldehyde, 97% | p-Formylpyridine | carbonyl-1,4-dihydropyridine | NSC 8953 | UNII-P577557492 | pyridine4-carboxaldehyd
Storage
Store at 2-8°C,Argon charged
Shipped In
Wet ice
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
5g
P105913-5g
2

9,90US$

14,90US$
Guardar 5,00 US$ (33.56%)
25g
P105913-25g
3

15,90US$

23,90US$
Guardar 8,00 US$ (33.47%)
100g
P105913-100g
3

46,90US$

70,90US$
Guardar 24,00 US$ (33.85%)
500g
P105913-500g
1

218,90US$

328,90US$
Guardar 110,00 US$ (33.44%)
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Why this grade

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

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Storage & shipping

Store at 2-8°C,Argon charged Ships Wet ice 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.

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Literature proof

Cited in 32 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

4-Pyridinecarboxaldehyde is a heterocyclic building block used to prepare Schiff bases via a Korich-type reaction.

Specifications

Sinónimos
4-pyridincarboxaldehyde | EC 212-832-3 | 4-pyrdinecarboxaldehyde | 4-pyridinecarbox-aldehyde | 4-pyridine carbaldehyde | 4-Pyridinecarboxaldehyde, 97% | p-Formylpyridine | carbonyl-1, 4-dihydropyridine | NSC 8953 | UNII-P577557492 | pyridine4-carboxaldehyd
Especificaciones y pureza
≥98%
Condiciones de almacenamiento de almacenamiento
Store at 2-8°C, Argon charged
Enviado en
Wet ice
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Pureza
≥98%
Nombres e identificadores
Sonrisas canónicasC1=CN=CC=C1C=O
IUPAC Namepyridine-4-carbaldehyde
InChIKeyBGUWFUQJCDRPTL-UHFFFAOYSA-N
INCHI1S/C6H5NO/c8-5-6-1-3-7-4-2-6/h1-5H
Isómeros SMILES C1=CN=CC=C1C=O
WGK Alemania 1
RTECS NR9400000
Número ONU 1993
Peso molecular 107.11
Beilstein 105342
Reaxy-Rn 105342
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=105342&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
SuperclassOrganoheterocyclic compounds
ClasePyridines and derivatives
SubclassPyridine carboxaldehydes
Intermediate Tree Nodes Not available
Direct ParentPyridine carboxaldehydes
Alternative Parents Aryl-aldehydes  Heteroaromatic compounds  Azacyclic compounds  Organopnictogen compounds  Organonitrogen compounds  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteromonocyclic compounds
Substituents 4-pyridine carboxaldehyde - Aryl-aldehyde - Heteroaromatic compound - Azacycle - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Aldehyde - Aromatic heteromonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as pyridine carboxaldehydes. These are aromatic compounds containing a pyridine ring which bears a carboxaldehyde group.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
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Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
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Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
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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.

24 results found

Lot NumberCertificate TypeFechaArticulo
D2621688Certificate of AnalysisMar 06, 2026 P105913
D2621687Certificate of AnalysisMar 06, 2026 P105913
D2621661Certificate of AnalysisMar 06, 2026 P105913
D2621684Certificate of AnalysisMar 06, 2026 P105913
H2205503Certificate of AnalysisFeb 04, 2026 P105913
H2205502Certificate of AnalysisFeb 04, 2026 P105913
G2215253Certificate of AnalysisJan 19, 2026 P105913
B2511360Certificate of AnalysisJan 07, 2025 P105913
B2511361Certificate of AnalysisJan 07, 2025 P105913
B2511362Certificate of AnalysisJan 07, 2025 P105913
B2511375Certificate of AnalysisJan 07, 2025 P105913
B2626085Certificate of AnalysisJan 07, 2025 P105913
A2607102Certificate of AnalysisJan 07, 2025 P105913
H2205501Certificate of AnalysisMay 20, 2024 P105913
D2415189Certificate of AnalysisFeb 29, 2024 P105913
C2330436Certificate of AnalysisApr 11, 2023 P105913
C2330405Certificate of AnalysisApr 11, 2023 P105913
C2330404Certificate of AnalysisApr 11, 2023 P105913
C2330403Certificate of AnalysisApr 11, 2023 P105913
J2417286Certificate of AnalysisApr 11, 2023 P105913
C2412059Certificate of AnalysisJun 30, 2022 P105913
G2314130Certificate of AnalysisJun 30, 2022 P105913
F2215122Certificate of AnalysisJun 21, 2022 P105913
D2014040Certificate of AnalysisFeb 21, 2022 P105913

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Propiedades químicas y físicas
SolubilidadSoluble in water (20 mg/ml at 20 °C), ethanol, and acetone.
SensibilidadAir and Light sensitive.
Índice de refracción1.5352
Punto de inflamación (°F)179.6 °F
Punto de inflamación (°C)54℃
Punto de ebullición (°C)198°C
Punto de fusión (°C)-2--4°C
Peso molecular107.110 g/mol
XLogP30.400
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count2
Rotatable Bond Count1
Exact Mass107.037 Da
Monoisotopic Mass107.037 Da
Topological Polar Surface Area30.000 Ų
Heavy Atom Count8
Formal Charge0
Complexity76.600
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
Preguntas frecuentes y artículos
Citations of This Product
Referencias
1. Ziming Qiao, Zhipeng Yang, Mengke Li, Yi Feng, Xiongwei Qu, Hemi Qu, Xiaojie Zhang.  (2023)  One-Pot Synthesis of Quaternary Pyridinium-Type Cationic-Based Porous Organic Frameworks: Enhanced Poly(ethylene oxide) Composite Polymer Electrolytes for All-Solid-State Li–S Batteries.  ACS Applied Energy Materials,      [PMID:] [10.1021/acsaem.3c02630]
2. Brian Musikavanhu, Zeping Huang, Quanhong Ma, Yongdi Liang, Zhaoli Xue, Lei Feng, Long Zhao.  (2023)  A pyridine modified naphthol hydrazone Schiff base chemosensor for Al3+ via intramolecular charge transfer process.  SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY,      [PMID:37290147] [10.1016/j.saa.2023.122961]
3. Yajuan Wang, Wenqiang Liu, Jiangxin Li, Juan Zhang.  (2022)  Preparation of porous macromolecule oxazine poly-ionic liquid solid acid catalyst and its application in an esterification reaction.  JOURNAL OF CHEMICAL TECHNOLOGY AND BIOTECHNOLOGY,  98  (1): (129-139).  [PMID:] [10.1002/jctb.7228]
4. Zheng Qu, Jiamin Huang, Guoliang Wu, Liangliang Dong, Chunfang Zhang, Yunxiang Bai.  (2022)  Tailor-made iron-organic molecular cage embedded polydimethylsiloxane membranes via emulsion casting technique for efficient VOCs removal.  JOURNAL OF APPLIED POLYMER SCIENCE,  139  (41): (e53004).  [PMID:] [10.1002/app.53004]
5. Yupeng Chen, Chong Chen, Xue Li, Nengjie Feng, Lei Wang, Hui Wan, Guofeng Guan.  (2022)  Hydroxyl-ionic liquid functionalized metalloporphyrin as an efficient heterogeneous catalyst for cooperative cycloaddition of CO2 with epoxides.  Journal of CO2 Utilization,      [PMID:] [10.1016/j.jcou.2022.102107]
6. Yuhao Chen, Zhonghua Chen, Yaowen Zhuo.  (2022)  Newly Synthesized Morpholinyl Mannich Bases as Corrosion Inhibitors for N80 Steel in Acid Environment.  Materials,  15  (12): (4218).  [PMID:35744277] [10.3390/ma15124218]
7. Boyi Chen, Zhongyuan Wang, Junsen Wang, Hailing Zheng, Junyi Zhou, Xushi Chen, Bing Wang, Yang Zhou, Zhiqin Peng.  (2021)  Ultrasensitive dual enhanced electrochemical immunosensor to detect ancient wool relics.  Analytical Methods,  14  (4): (394-400).  [PMID:34981794] [10.1039/D1AY01514A]
8. Xin Lai, Jianfeng Hu, Tao Ruan, Jianhui Zhou, Jinqing Qu.  (2021)  Chitosan derivative corrosion inhibitor for aluminum alloy in sodium chloride solution: A green organic/inorganic hybrid.  CARBOHYDRATE POLYMERS,      [PMID:33966838] [10.1016/j.carbpol.2021.118074]
9. Yue Zhang, Lin Liu, Wei-Guo Xu, Zheng-Bo Han.  (2021)  MOF@POP core–shell architecture as synergetic catalyst for high-efficient CO2 fixation without cocatalyst under mild conditions.  Journal of CO2 Utilization,      [PMID:] [10.1016/j.jcou.2021.101463]
10. Hengye Chen, Liuna Wei, Xiaoming Guo, Chengying Hai, Lu Xu, Lei Zhang, Wei Lan, Chunsong Zhou, Yuanbin She, Haiyan Fu.  (2020)  Determination of l-theanine in tea water using fluorescence-visualized paper-based sensors based on CdTe quantum dots/corn carbon dots and nano-porphyrin with chemometrics.  JOURNAL OF THE SCIENCE OF FOOD AND AGRICULTURE,  101  (6): (2552-2560).  [PMID:33063338] [10.1002/jsfa.10882]
11. Shichao Xu, Xiaojing Zeng, Songlin Dai, Jing Wang, Yuxiang Chen, Jie Song, Yunfei Shi, Xian Cheng, Shengliang Liao, Zhendong Zhao.  (2020)  Turpentine Derived Secondary Amines for Sustainable Crop Protection: Synthesis, Activity Evaluation and QSAR Study.  JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY,      [PMID:32975941] [10.1021/acs.jafc.0c01909]
12. Song Liu, Zhen-jie Huang, Feng Li, Wei-jing Zhang, Chun-rong Zhu, Cheng-bin Gong, Jun-fei Long, Qian Tang.  (2020)  Star-shaped monosubstituted 2,6-diphenyl-4,4′-bipyridinium salts with good electrochromic switching stability.  SYNTHETIC METALS,      [PMID:] [10.1016/j.synthmet.2020.116330]
13. Dongmei He, Li Zeng, Guiqing Zhang, Wenjuan Guan, Zuoying Cao, Qinggang Li, Shengxi Wu.  (2019)  Extraction behavior and mechanism of nickel in chloride solution using a cleaner extractant.  Journal of Cleaner Production,      [PMID:] [10.1016/j.jclepro.2019.118517]
14. Xu Han, Jilin Wang, Lulu Wang.  (2018)  Preparation of anion exchange membranes based on pyridine functionalized poly(vinyl alcohol) crosslinked by 1,4-dichlorobutane.  JOURNAL OF APPLIED POLYMER SCIENCE,  136  (16): (47395).  [PMID:] [10.1002/app.47395]
15. Chunfang Zhang, Xuejian Si, Shuo Zhang, Bei Pei, Jin Gu, Yunxiang Bai.  (2018)  Porous metal–organic molecular cage: a promising candidate to highly improve the nanofiltration performance of thin film nanocomposite membranes.  NEW JOURNAL OF CHEMISTRY,  43  (4): (1699-1709).  [PMID:] [10.1039/C8NJ04603D]
16. Tingting Xiao, Xiaoyang Zhang, Jingyu Wu, Jiazhi Yang, Yong Yang.  (2017)  Aliphatic-Alcohol-Induced Opaque-to-Transparent Transformation and Application of Solubility Theory in a Bis-Dipeptide-Based Supramolecular Gel.  ChemPlusChem,  82  (6): (879-887).  [PMID:31961561] [10.1002/cplu.201700206]
17. He Li, Chunzhi Li, Jian Chen, Lina Liu, Qihua Yang.  (2017)  Synthesis of a Pyridine–Zinc-Based Porous Organic Polymer for the Co-catalyst-Free Cycloaddition of Epoxides.  Chemistry-An Asian Journal,  12  (10): (1095-1103).  [PMID:28326679] [10.1002/asia.201700258]
18. Xiuquan Jia, Jiping Ma, Min Wang, Xiaofang Li, Jin Gao, Jie Xu.  (2016)  Alkali α-MnO2/NaxMnO2 collaboratively catalyzed ammoxidation–Pinner tandem reaction of aldehydes.  Catalysis Science & Technology,  (20): (7429-7436).  [PMID:] [10.1039/C6CY00874G]
19. Weifen Niu, Ming Nan, Li Fan, Man Shing Wong, Shaomin Shuang, Chuan Dong.  (2015)  A novel pH fluorescent probe based on indocyanine for imaging of living cells.  DYES AND PIGMENTS,      [PMID:] [10.1016/j.dyepig.2015.11.027]
20. Gang Liu, Mingdi Yang, Lianke Wang, Jun Zheng, Hongping Zhou, Jieying Wu, Yupeng Tian.  (2014)  Schiff base derivatives containing heterocycles with aggregation-induced emission and recognition ability.  Journal of Materials Chemistry C,  (15): (2684-2691).  [PMID:] [10.1039/C3TC32591A]
21. Xuan Kuang, Yu Ma, Hao Su, Jine Zhang, Yu-Bin Dong, Bo Tang.  (2014)  High-Performance Liquid Chromatographic Enantioseparation of Racemic Drugs Based on Homochiral Metal–Organic Framework.  ANALYTICAL CHEMISTRY,      [PMID:24380495] [10.1021/ac403674p]
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