C2204
ε-己内酰胺
99%
别名:
2-酮基六亚基亚胺, 环己酮异肟
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经验公式（希尔记法）:
C6H11NO
化学文摘社编号:
分子量:
113.16
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-313-2
Beilstein/REAXYS Number:
106934
MDL number:
产品名称
ε-己内酰胺, 99%
assay
99%
InChI key
JBKVHLHDHHXQEQ-UHFFFAOYSA-N
InChI
1S/C6H11NO/c8-6-4-2-1-3-5-7-6/h1-5H2,(H,7,8)
SMILES string
O=C1CCCCCN1
vapor pressure
<0.01 mmHg ( 20 °C)
form
crystals
autoignition temp.
707 °F
expl. lim.
8 %
bp
136-138 °C/10 mmHg (lit.)
mp
68-71 °C (lit.)
Quality Level
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Application
ε-己内酰胺可用作开环聚合生产尼龙-6反应的前体。它还可在阴离子催化剂的存在下，通过ε己内酰胺微波辐照合成聚(ε己内酰胺-co-ε-己内酯)。
signalword
Warning
Hazard Classifications
Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
305.6 °F - closed cup
flash_point_c
152 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
?-Caprolactam: New by-product free synthesis routes
Dahlhoff, G, et al.
Catalysis Reviews: Science and Engineering, 43(4), 381-441 (2001)
Design of a ?green? one-step catalytic production of ?-caprolactam (precursor of nylon-6)
Thomas JM and Raja R
Proceedings of the National Academy of Sciences of the USA, 102(39), 13732-13736 (2005)
Microwave syntheses of poly (?-caprolactam-co-?-caprolactone)
Fang X, et al.
Journal of Polymer Science Part A: Polymer Chemistry, 38(8), 1379-1390 (2000)
Ibrahim I Ozturk et al.
Journal of inorganic biochemistry, 109, 57-65 (2012-03-02)
Three new antimony(III) halide complexes (SbX(3), X=Cl, Br and I) with the heterocyclic thione ω-thiocaprolactam (1-azacycloheptane-2-thione, (Hthcl)) of formulae {[SbCl(2)(μ(2)-Cl)(Hthcl)(2)](n)} (1), {[(SbBr(2)(μ(2)-Br)(Hthcl)(2))(2)]} (2) and {[(SbI(2)(μ(2)-I)(Hthcl)(2))(2)]} (3) were synthesized from the reaction of antimony(III) halides with ω-thiocaprolactam in 1:2 stoichiometry. The
Ahmad Bitar et al.
Journal of biomedical nanotechnology, 8(5), 709-719 (2012-08-15)
Temperature and glucose sensitive microgels were prepared via radical precipitation polymerization, using N-vinylcaprolactam (NVCL) as the main monomer, N,N-methylenebisacrylamide (MBA) as a crosslinker, V50 as initiator and 4-vinylphenylboronic acid (VPBA) as a functional monomer. The LCST of homopoly (NVCL) was
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