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N-Acetylcaprolactam

Name: <I>N</I>-Acetylcaprolactam
Brand: ALDRICH

99%

Synonym(s):

1-Acetyl-2-oxohexamethyleneimine, 1-Acetylhexahydro-2H-azepin-2-one

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About This Item

Empirical Formula (Hill Notation):

C₈H₁₃NO₂

CAS Number:

1888-91-1

Molecular Weight:

155.19

Beilstein:

119598

EC Number:

217-565-6

MDL number:

MFCD00003262

UNSPSC Code:

12352100

PubChem Substance ID:

24856858

NACRES:

NA.22

Quality Level

100

Assay

99%

refractive index

n20/D 1.489 (lit.)

bp

134-135 °C/26 mmHg (lit.)

density

1.094 g/mL at 25 °C (lit.)

SMILES string

CC(=O)N1CCCCCC1=O

InChI

1S/C8H13NO2/c1-7(10)9-6-4-2-3-5-8(9)11/h2-6H2,1H3

InChI key

QISSLHPKTCLLDL-UHFFFAOYSA-N

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Related Categories

Organic Building Blocks

Application

N-Acetylcaprolactam has been used:

as initiator to investigate kinetics of anionic polymerization of ε-caprolactam
in ring-opening polymerization of nylon 6

Pictograms

GHS07

Signal Word

Warning

Hazard Statements

H302,H319

Precautionary Statements

P264 - P270 - P280 - P301 + P312 - P305 + P351 + P338 - P337 + P313

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2

WGK

WGK 1

Flash Point(F)

closed cup

Flash Point(C)

closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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The kinetic equation for the initiated, anionic polymerization of ?-caprolactam.

Greenley RZ, et al.

Macromolecules, 2(6), 561-567 (1969)

Effect of composite preparation techniques on electrical and mechanical properties and morphology of nylon 6 based conductive polymer composites.

Koysuren O, et al.

Journal of Applied Polymer Science, 102(3), 2520-2526 (2006)

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