Caprolactam - CP , CAS No.105-60-2

CAS: 105-60-2 Cat. No.: C111698 Fórmula: C6H11NO Peso molecular: 113.16 Beilstein Registry Number: 106934 Número EC: 203-313-2
Disponible para pedir
GRADE & PURITY CP ? Chemically Pure grade — moderate purity above technical grade but below analytical. Use for general lab reactions where ultra-low impurities aren't critical.
Synonyms
Caprolon B | e-Kaprolaktam | Hexahydro-2H-azepin-2-one | 6-Caprolactam | hexahydro 2H Azepin 2 one | NSC-117393 | Tarnamid T | 2-Oxohexamethylenimine | caprolactim | Stylon | UNII-6879X594Z8 | .epsilon.-Caprolactam | AI3-14515 | cis-Hexahydro-2-azepinone
Storage
Room temperature,Argon charged
Shipped In
Normal
★
Size
USA
Alemania (EU)*
Price
Qty
100g
C111698-100g
3 Disponible
—
9,90US$
250g
C111698-250g
2 Disponible
1 Disponible

11,90US$

14,90US$
Guardar 3,00 US$ (20.13%)
500g
C111698-500g
Fabricado bajo pedido · 8–12 semanas

14,90US$

19,90US$
Guardar 5,00 US$ (25.13%)
Enter a quantity for the sizes you want to add.
🧪
Why this grade

CP CP for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature,Argon charged 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 57 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinónimos
Caprolon B | e-Kaprolaktam | Hexahydro-2H-azepin-2-one | 6-Caprolactam | hexahydro 2H Azepin 2 one | NSC-117393 | Tarnamid T | 2-Oxohexamethylenimine | caprolactim | Stylon | UNII-6879X594Z8 | .epsilon.-Caprolactam | AI3-14515 | cis-Hexahydro-2-azepinone
Especificaciones y pureza
CP
Condiciones de almacenamiento de almacenamiento
Room temperature,Argon charged
Enviado en
Normal
Grado
CP
Nombres e identificadores
Sonrisas canónicas
C1CCC(=O)NCC1
IUPAC Name
azepan-2-one
InChIKey
JBKVHLHDHHXQEQ-UHFFFAOYSA-N
INCHI
1S/C6H11NO/c8-6-4-2-1-3-5-7-6/h1-5H2,(H,7,8)
Isómeros SMILES
C1CCC(=O)NCC1
WGK Alemania
1
RTECS
CM3675000
Peso molecular
113.16
Beilstein
106934
Reaxy-Rn
106934
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=106934&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
ClaseLactams
SubclassCaprolactams
Intermediate Tree Nodes Not available
Direct ParentCaprolactams
Alternative Parents Azepanes  Secondary carboxylic acid amides  Azacyclic compounds  Organopnictogen compounds  Organonitrogen compounds  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic heteromonocyclic compounds
Substituents Caprolactam - Azepane - Secondary carboxylic acid amide - Carboxamide group - Azacycle - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Carbonyl group - Aliphatic heteromonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as caprolactams. These are cyclic amides of caproic acid. Caproic acid is the carboxylic acid derived from hexane with the general formula C5H11COOH.
External Descriptors a lactam
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (no humanos)
Mus musculus (284745 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.

21 results found

Lot NumberCertificate TypeFechaArticulo
H2631238Certificate of AnalysisSep 10, 2026 C111698
G2609143Certificate of AnalysisJul 21, 2026 C111698
G2220423Certificate of AnalysisMay 09, 2026 C111698
A2606193Certificate of AnalysisJan 10, 2026 C111698
A2606195Certificate of AnalysisJan 10, 2026 C111698
L2511093Certificate of AnalysisDec 25, 2025 C111698
L2115467Certificate of AnalysisSep 17, 2025 C111698
H2505239Certificate of AnalysisAug 14, 2025 C111698
H2505240Certificate of AnalysisAug 14, 2025 C111698
I2102131Certificate of AnalysisJun 09, 2025 C111698
C2531228Certificate of AnalysisApr 18, 2025 C111698
C2531121Certificate of AnalysisApr 18, 2025 C111698
F2412169Certificate of AnalysisJun 15, 2024 C111698
F2412170Certificate of AnalysisJun 15, 2024 C111698
C2420049Certificate of AnalysisMar 22, 2024 C111698
A2417251Certificate of AnalysisFeb 01, 2024 C111698
J2318801Certificate of AnalysisNov 01, 2023 C111698
H2303411Certificate of AnalysisAug 14, 2023 C111698
H2303415Certificate of AnalysisAug 14, 2023 C111698
G2308172Certificate of AnalysisJul 13, 2023 C111698
G2220424Certificate of AnalysisSep 01, 2022 C111698
Propiedades químicas y físicas
SolubilidadSoluble in water, soluble in most organic solvents such as ethanol, ether, chloroform, etc.
SensibilidadMoisture sensitive
Índice de refracción1.4935
Punto de inflamación (°F)305.6 °F
Punto de inflamación (°C)125 °C
Punto de ebullición (°C)136-138 °C/10 mmHg (lit.)
Punto de fusión (°C)68-71°C
Peso molecular113.160 g/mol
XLogP3-0.100
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count1
Rotatable Bond Count0
Exact Mass113.084 Da
Monoisotopic Mass113.084 Da
Topological Polar Surface Area29.100 Ų
Heavy Atom Count8
Formal Charge0
Complexity90.500
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
Picking CP Grade Reagents: Applications, Limits, and Upgrade Paths
The Role of 7-Membered Nitrogen Heterocycles in Drug Discovery: Microstate Management, Conformational Bias, and Developability Trade-offs (with Research Selection Navigator and Product Tables 1–3)
From Piperidine to Homopiperidine: How a Seven-Membered Nitrogen Ring Redirects Substituent Vectors and Shifts Salt Formation/Solubility Behavior (Tables 1–3)
Adding a Temperature-Triggered Switch to NCO: How Blocked Isocyanates Affect the Storage, Curing, and Film Performance of 1K Baking Coatings
1K, 2K, Waterborne, Moisture-Curing, and Blocked Systems: Classification Logic and Identification Methods for Polyurethane Coating Curing Systems
Key Control Points in Polyurethane Coating Formulation Design and Application
Film Formation and Curing Mechanisms of Polyester Resins for Coatings: From Functional Groups and Curing Systems to Crosslinked Networks
From Water to Film: Film-Formation Mechanisms and Performance Development of Waterborne Emulsions and Dispersions
Citations of This Product
Calculadoras de soluciones
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