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N12483

N-(2-Ethylhexyl)-5-norbornene-2,3-dicarboximide

analytical standard

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About This Item

Empirical Formula (Hill Notation):
C17H25NO2
CAS Number:
113-48-4
Molecular Weight:
275.39
EC Number:
204-029-1
MDL number:
MFCD00072467
UNSPSC Code:
41116107
PubChem Substance ID:
329818541
Pricing and availability is not currently available.

grade

analytical standard

packaging

ampule of 250 mg

manufacturer/tradename

Chem Service, Inc. PS-962

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

format

neat

SMILES string

CCCCC(CC)CN1C(=O)C2[C@H]3C[C@H](C=C3)C2C1=O

InChI

1S/C17H25NO2/c1-3-5-6-11(4-2)10-18-16(19)14-12-7-8-13(9-12)15(14)17(18)20/h7-8,11-15H,3-6,9-10H2,1-2H3/t11?,12-,13+,14?,15?

InChI key

WLLGXSLBOPFWQV-OTHKPKEBSA-N

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Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Pictograms

Skull and crossbonesEnvironment
GHS06,GHS09

Signal Word

Danger

Hazard Statements

H311,H317,H332,H411

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 4 Inhalation - Aquatic Chronic 2 - Skin Sens. 1B

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flash Point(F)

350.6 °F - closed cup

Flash Point(C)

177 °C - closed cup

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I-Hsiung Wang et al.
Journal of chromatography. A, 983(1-2), 145-152 (2003-02-06)
An isocratic reversed-phase high-performance liquid chromatographic (RP-HPLC) method development for the simultaneous determination of five active ingredients (S)-methoprene, MGK264, PBO, sumithrin and permethrin in a new complex pesticide formulation is described. These active ingredients have similar polarities and contain isomers.
Effects of synergists on bendiocarb and pyrethrins resistance in the German cockroach (Dictyoptera: Blattellidae).
D G Cochran
Journal of economic entomology, 80(4), 728-732 (1987-08-01)
I H Wang et al.
Journal of chromatography. A, 864(2), 271-281 (2000-02-11)
N-Octyl bicycloheptene dicarboximide (MGK 264) has exo and endo diastereomers. Each structure has a chiral center at the nitrogen side chain. Enantioselective separation of MGK 264 was achieved by normal-phase high-performance liquid chromatography (HPLC) using cellulose-based Chiralcel OD column with
G L Zellers et al.
Annals of emergency medicine, 19(3), 327-329 (1990-03-01)
A man experienced one hour and 40 minutes of continual, inappropriate, uncontrollable laughter. The onset was preceded by a single-inhalation exposure to an insecticide of very low toxicity. The episode was terminated by a single dose of IV diazepam. A
H S Radwan et al.
Toxicology, 14(3), 193-198 (1979-11-01)
Piperonyl butoxide, sulfoxide and MGK 264 were found to act as synergists for certain organotin compounds; with respect to their toxicity on the larvae of a susceptible strain of the cotton leafworm, Spodoptera littoralis (Boisd.). High degree of synergism was
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