Caprolactam - ≥99% , CAS No.105-60-2

CAS: 105-60-2 Cat. No.: C111700 Formule: C6H11NO Poids moléculaire: 113.16 Beilstein Registry Number: 106934 Numéro CE: 203-313-2
DISPONIBLE À COMMANDE
GRADE & PURITY ≥99%
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
Allemagne (EU)
USA*
Price
Qty
100g
C111700-100g
—
3 En stock
13,80€
500g
C111700-500g
—
3 En stock
21,61€
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,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.

Vue d’ensemble

ε-Caprolactam can be used as a precursor for the production of nylon-6 by ring-opening polymerization.It is also microwave irradiated with ε caprolactone in the presence of an anionic catalyst to yield poly(ε caprolactam-co-ε-caprolactone).

Specifications

Synonymes
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
Spécifications et pureté
≥99%
Conditions de stockage de stockage
Room temperature,Argon charged
Expédié en
Normal
Pureté
≥99%
Noms et identifiants
Pubchem Sid
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/504751451
Sourires canoniques
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)
Isomères SMILES
C1CCC(=O)NCC1
WGK Allemagne
1
RTECS
CM3675000
Poids moléculaire
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
ClasseLactams
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
DescriptionThis 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
Structure 3D
Modèle de structure chimique interactif





Cibles associées (non humaines)
Mus musculus (284745 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mécanismes d'action
Certificats (CoA, COO, BSE/TSE et tableau d'analyse)
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.

51 results found

Lot NumberCertificate TypeDateArticle
H2631256Certificate of AnalysisAug 18, 2026 C111700
H2631255Certificate of AnalysisAug 18, 2026 C111700
H2631239Certificate of AnalysisAug 18, 2026 C111700
H2631237Certificate of AnalysisAug 18, 2026 C111700
E2614256Certificate of AnalysisApr 29, 2026 C111700
E2614184Certificate of AnalysisApr 29, 2026 C111700
E2614177Certificate of AnalysisApr 29, 2026 C111700
E2614176Certificate of AnalysisApr 29, 2026 C111700
G2606103Certificate of AnalysisApr 29, 2026 C111700
A2606189Certificate of AnalysisDec 24, 2025 C111700
A2606190Certificate of AnalysisDec 24, 2025 C111700
A2606191Certificate of AnalysisDec 24, 2025 C111700
A2606192Certificate of AnalysisDec 24, 2025 C111700
A2606194Certificate of AnalysisDec 24, 2025 C111700
H2505237Certificate of AnalysisJun 24, 2025 C111700
H2505238Certificate of AnalysisJun 24, 2025 C111700
H2505236Certificate of AnalysisJun 24, 2025 C111700
H2505168Certificate of AnalysisJun 24, 2025 C111700
C2531364Certificate of AnalysisMar 19, 2025 C111700
C2531230Certificate of AnalysisMar 19, 2025 C111700
C2531229Certificate of AnalysisMar 19, 2025 C111700
C2531123Certificate of AnalysisMar 19, 2025 C111700
C2531122Certificate of AnalysisMar 19, 2025 C111700
J2410428Certificate of AnalysisSep 20, 2024 C111700
J2410279Certificate of AnalysisSep 20, 2024 C111700
J2410429Certificate of AnalysisSep 20, 2024 C111700
B2506091Certificate of AnalysisSep 20, 2024 C111700
K2425273Certificate of AnalysisJul 19, 2024 C111700
K2425271Certificate of AnalysisJul 19, 2024 C111700
K2425272Certificate of AnalysisJul 19, 2024 C111700
F2412232Certificate of AnalysisMay 28, 2024 C111700
F2412172Certificate of AnalysisMay 28, 2024 C111700
F2412171Certificate of AnalysisMay 28, 2024 C111700
D2418597Certificate of AnalysisMar 25, 2024 C111700
D2418595Certificate of AnalysisMar 25, 2024 C111700
D2418593Certificate of AnalysisMar 25, 2024 C111700
A2417253Certificate of AnalysisJan 05, 2024 C111700
A2417254Certificate of AnalysisJan 05, 2024 C111700
A2417252Certificate of AnalysisJan 05, 2024 C111700
H2303561Certificate of AnalysisJul 15, 2023 C111700
H2303511Certificate of AnalysisJul 15, 2023 C111700
H2303444Certificate of AnalysisJul 15, 2023 C111700
D23191143Certificate of AnalysisApr 10, 2023 C111700
D23191137Certificate of AnalysisApr 10, 2023 C111700
D23191133Certificate of AnalysisApr 10, 2023 C111700
D23191132Certificate of AnalysisApr 10, 2023 C111700
L22151167Certificate of AnalysisDec 20, 2022 C111700
G2220441Certificate of AnalysisJun 08, 2022 C111700
G2220422Certificate of AnalysisJun 08, 2022 C111700
G2220421Certificate of AnalysisJun 08, 2022 C111700
G2220420Certificate of AnalysisJun 08, 2022 C111700
Propriétés chimiques et physiques
SolubilitéSoluble in benzene, ethanol, water, chloroform, methanol, tetrahydrofurfuryl alcohol, ether, dimethylformamide, chlorinated hydrocarbons, cyclohexene and petroleum fractions.
SensibilitéMoisture sensitive
Indice de réfraction1.4935
Point d'éclair (°F)305.6 °F
Point d'éclair (°C)125 °C
Point d'ébullition (°C)136-138 °C/10 mmHg (lit.)
Point de fusion (°C)68-71°C
Poids moléculaire113.160 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
FAQ et articles
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
Caprolactam Handling & Solution Preparation Protocol
Citations of This Product
Calculateurs de solution
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