4-Pyridinecarbonitrile - ≥98% , CAS No.100-48-1

CAS: 100-48-1 Cat. No.: P110335 Peso molecular: 104.11 Beilstein Registry Number: 107712 Número EC: 202-856-2
Disponible para pedir
GRADE & PURITY ≥98%
Synonyms
EN300-18319 | NSC60681 | NSC-60681 | GPHQHTOMRSGBNZ-UHFFFAOYSA- | Q27274960 | D77982 | NCGC00254647-01 | EINECS 202-856-2 | DS-16750 | InChI=1/C6H4N2/c7-5-6-1-3-8-4-2-6/h1-4H | pyridine-4-carbonitrile | 4-Pyridinecarbonitrile, purum, >=96.0% (GC) | SB5223
Storage
Argon charged,Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
25g
P110335-25g
≥10
9,90US$
100g
P110335-100g
2
10,90US$
500g
P110335-500g
2

33,90US$

50,90US$
Guardar 17,00 US$ (33.40%)
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

Argon charged,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 11 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinónimos
EN300-18319 | NSC60681 | NSC-60681 | GPHQHTOMRSGBNZ-UHFFFAOYSA- | Q27274960 | D77982 | NCGC00254647-01 | EINECS 202-856-2 | DS-16750 | InChI=1/C6H4N2/c7-5-6-1-3-8-4-2-6/h1-4H | pyridine-4-carbonitrile | 4-Pyridinecarbonitrile, purum, >=96.0% (GC) | SB5223
Especificaciones y pureza
≥98%
Condiciones de almacenamiento de almacenamiento
Argon charged, Room temperature
Enviado en
Normal
Pureza
≥98%
Nombres e identificadores
Pubchem Sid488180467
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488180467
Sonrisas canónicasC1=CN=CC=C1C#N
IUPAC Namepyridine-4-carbonitrile
InChIKeyGPHQHTOMRSGBNZ-UHFFFAOYSA-N
INCHI1S/C6H4N2/c7-5-6-1-3-8-4-2-6/h1-4H
Isómeros SMILES C1=CN=CC=C1C#N
WGK Alemania 3
Peso molecular 104.11
Beilstein 107712
Reaxy-Rn 107712
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=107712&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
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentPyridines and derivatives
Alternative Parents Heteroaromatic compounds  Nitriles  Azacyclic compounds  Organopnictogen compounds  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteromonocyclic compounds
Substituents Pyridine - Heteroaromatic compound - Azacycle - Nitrile - Carbonitrile - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteromonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as pyridines and derivatives. These are compounds containing a pyridine ring, which is a six-member aromatic heterocycle which consists of one nitrogen atom and five carbon atoms.
External Descriptors cyanopyridine
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (no humanos)
Pseudomonas aeruginosa (123386 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Acinetobacter baumannii (41033 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Frankliniella occidentalis (90 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Thrips tabaci (33 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
G2222860Certificate of AnalysisMay 09, 2026 P110335
G2222866Certificate of AnalysisMay 09, 2026 P110335
K2123581Certificate of AnalysisSep 04, 2025 P110335
I2130031Certificate of AnalysisJul 10, 2025 P110335
K1708053Certificate of AnalysisJun 12, 2025 P110335
G2405271Certificate of AnalysisApr 28, 2024 P110335
G2405272Certificate of AnalysisApr 28, 2024 P110335
K2521069Certificate of AnalysisAug 10, 2023 P110335
H2328787Certificate of AnalysisAug 10, 2023 P110335
H2328786Certificate of AnalysisAug 10, 2023 P110335
H2328785Certificate of AnalysisAug 10, 2023 P110335
H2328706Certificate of AnalysisAug 10, 2023 P110335
B2317916Certificate of AnalysisJan 10, 2023 P110335
B2317915Certificate of AnalysisJan 10, 2023 P110335
B2317914Certificate of AnalysisJan 10, 2023 P110335
B2317913Certificate of AnalysisJan 10, 2023 P110335
B2317912Certificate of AnalysisJan 10, 2023 P110335
B2317911Certificate of AnalysisJan 10, 2023 P110335
G2222867Certificate of AnalysisJun 10, 2022 P110335
G2222823Certificate of AnalysisJun 10, 2022 P110335

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Propiedades químicas y físicas
SolubilidadSoluble in water.
SensibilidadHygroscopic.
Punto de inflamación (°F)88 °C
Punto de inflamación (°C)88°C
Punto de ebullición (°C)196°C
Punto de fusión (°C)77-81°C
Peso molecular104.110 g/mol
XLogP30.500
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count2
Rotatable Bond Count0
Exact Mass104.037 Da
Monoisotopic Mass104.037 Da
Topological Polar Surface Area36.700 Ų
Heavy Atom Count8
Formal Charge0
Complexity105.000
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
Preguntas frecuentes y artículos
Citations of This Product
Referencias
1. Yangyang Sun, Zhuzhu Tang, Yanjun Li, Yongkang Song, Hualei Wang, Dongzhi Wei, Shengli Yang.  (2023)  Identification and evolution of non-traditional nitrilase from Spirosoma linguale DSM 74 with high hydration activity.  BIOORGANIC CHEMISTRY,      [PMID:38185008] [10.1016/j.bioorg.2023.107055]
2. Junling Guo, Zhongyi Cheng, Lukasz Peplowski, Zhemin Zhou.  (2023)  Highly efficient biosynthesis of isonicotinamide through a substrate access tunnel engineered nitrile hydratase from Carbonactinospora thermoautotrophicus.  NEW JOURNAL OF CHEMISTRY,  47  (28): (13279-13285).  [PMID:] [10.1039/D3NJ00331K]
3. Guixiang Yang, Yuwei Wang, Ye Li, Chenglu Yan, Zhenxi Liu, Huiyong Wang, Huaqiao Peng, Juan Du, Baozhan Zheng, Yong Guo.  (2022)  Synthesis of Vitamin B1-Stabilized Gold Nanoclusters with High Quantum Yields for Application as Sensors.  ACS Applied Nano Materials,      [PMID:] [10.1021/acsanm.2c04289]
4. Min Zhang, Dong Peng, Feifei Peng, Anwei Huang, Kaiqiang Song, Qingbing He, Changqing Yin, Jinsong Rao, Yuxin Zhang, Haitao Chen, Dalong Cong, Zhongsheng Li.  (2021)  Effects of Additives Containing Cyanopyridine on Electrodeposition of Bright Al Coatings from AlCl3-EMIC Ionic Liquids.  Coatings,  11  (11): (1396).  [PMID:] [10.3390/coatings11111396]
5. Zhishan Luo, Min Zhou, Xinchen Wang.  (2018)  Cobalt-based cubane molecular co-catalysts for photocatalytic water oxidation by polymeric carbon nitrides.  APPLIED CATALYSIS B-ENVIRONMENTAL,      [PMID:] [10.1016/j.apcatb.2018.07.056]
6. Guojian Chen, Xiaochen Wang, Jing Li, Wei Hou, Yu Zhou, Jun Wang.  (2015)  Direct Carbonization of Cyanopyridinium Crystalline Dicationic Salts into Nitrogen-Enriched Ultra-Microporous Carbons toward Excellent CO2 Adsorption.  ACS Applied Materials & Interfaces,      [PMID:26234297] [10.1021/acsami.5b04842]
7. Xiaolin Pei, Lirong Yang, Gang Xu, Qiuyan Wang, Jianping Wu.  (2013)  Discovery of a new Fe-type nitrile hydratase efficiently hydrating aliphatic and aromatic nitriles by genome mining.  JOURNAL OF MOLECULAR CATALYSIS B-ENZYMATIC,      [PMID:] [10.1016/j.molcatb.2013.10.015]
8. Meng Zhao, Yun Yang, Xue-Song Gu, Lanlan Sun.  (2024)  Interior precisely designed metal–organic framework for light hydrocarbons separation.  POLYHEDRON,      [PMID:] [10.1016/j.poly.2024.116917]
9. Rui Xue, Rong Qiang, Yulong Shao, Xiao Yang, Qian Ma, Yi Chen, Fangjie Ren, Yuancheng Ding, Bowen Chen, Shijiang Feng.  (2024)  MoS2-Decorated Tubular Carbon Nanostructures with Enhanced Dielectric Loss for Boosting Microwave Absorption.  ACS Applied Nano Materials,      [PMID:] [10.1021/acsanm.4c01930]
10. Yingxuan Wen, Fangfang Zhang, Jingru Dou, Shougui Wang, Fei Gao, Falong Shan, Jipeng Dong, Guanghui Chen.  (2024)  Multifunctional ionic covalent triazine framework as heterogeneous catalysts for efficient CO2 cycloaddition.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2024.130579]
11. Jinghua Huang, Mingbao Huang, Jinan Li, Jie Zhang, Zhiyong Fu.  (2025)  New Thermoelectricity Utilization System Based on Aqueous Organic Redox Flow Battery Involving the Tripyridinium–Triazine Radicals.  CHEMISTRY-A EUROPEAN JOURNAL,      [PMID:40105032] [10.1002/chem.202500237]
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