C102202
Cyclohexanone oxime
97%
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100 G
$46.90
500 G
$113.00
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100 G
$46.90
500 G
$113.00
About This Item
Fórmula lineal:
C6H10(=NOH)
Número de CAS:
Peso molecular:
113.16
Beilstein/REAXYS Number:
1616769
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
assay
97%
form
crystals
bp
206-210 °C (lit.)
mp
86-89 °C (lit.)
SMILES string
O\N=C1/CCCCC1
InChI
1S/C6H11NO/c8-7-6-4-2-1-3-5-6/h8H,1-5H2
InChI key
VEZUQRBDRNJBJY-UHFFFAOYSA-N
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signalword
Warning
hcodes
pcodes
Hazard Classifications
Acute Tox. 4 Oral
Storage Class
11 - Combustible Solids
wgk_germany
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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S Ramalingam et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 96, 207-220 (2012-06-12)
In the present analysis, FT-IR/FT-Raman spectra of the cyclohexanone oxime (CHO, C(6)H(11)NO) are recorded. The observed vibrational frequencies are assigned and the computational calculations are carried out by HF and DFT (B3LYP and B3PW91) methods with 6-311++G(d,p) basis set and
Moa Andresen Bergström et al.
Journal of medicinal chemistry, 51(8), 2541-2550 (2008-03-29)
Metabolic activation of chemicals (prohaptens) in the skin can cause allergic contact dermatitis. We have explored structure-allergenic activity relationships for seven potential oxime prohaptens using the local lymph node assay and a GSH trapping screen with liver microsomes. The general
M J Derelanko et al.
Fundamental and applied toxicology : official journal of the Society of Toxicology, 5(1), 117-127 (1985-02-01)
Cyclohexanone oxime (CHO) was given po to male and female Fischer 344 rats at dose levels of 10, 25, 75, 150, and 300 mg/kg, five times a week for a period of 2 weeks. Control animals received distilled water. All
R E Glover et al.
Chemical research in toxicology, 12(10), 952-957 (1999-10-20)
Cyclohexanone oxime (CHOX), an intermediate used in the synthesis of polycaprolactam (Nylon-6), has been reported to be hematotoxic in Fischer rats. The in vivo metabolism of CHOX was found to release nitric oxide, which was detected in venous blood by
D Parmar et al.
Drug metabolism and disposition: the biological fate of chemicals, 19(6), 1101-1107 (1991-11-01)
Cyclohexanone oxime (CHOX), an intermediate used in the synthesis of Polycaprolactam/Nylon, was found to be rapidly absorbed and cleared from the body within 24 hours after a single oral administration of 1, 10 and 30 mg/kg of [14C]-CHOX to the
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