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C102202

Sigma-Aldrich

Cyclohexanone oxime

97%

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About This Item

Linear Formula:
C6H10(=NOH)
CAS Number:
Molecular Weight:
113.16
Beilstein:
1616769
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

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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Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Precautionary Statements

Hazard Classifications

Acute Tox. 4 Oral

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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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
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
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
N G Palmen et al.
Archives of toxicology, 72(5), 270-276 (1998-06-18)
Both oximes and hydroxylamine (HYAM) are compounds with known oxidative capacity. We tested in vitro whether acetaldoxime (AAO), cyclohexanone oxime (CHO), methyl ethyl ketoxime (MEKO) or HYAM affect haemoglobin oxidation (into HbFe3+), formation of thiobarbituric acid reactive substances (TBARS), and
Shelli J Schomaker et al.
Toxicology and applied pharmacology, 185(1), 48-54 (2002-12-04)
The purpose of these studies was to evaluate bone marrow from male CD rats following exposure to known hematotoxins using flow cytometry (FC) and a monoclonal antibody to the cell surface antigen CD71. Rats were treated with either CHO (300

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