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36732

Supelco

1-Naphthylacetamide

PESTANAL®, analytical standard

Synonym(s):

1-Naphthaleneacetamide

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About This Item

Linear Formula:
C10H7CH2CONH2
CAS Number:
86-86-2
Molecular Weight:
185.22
Beilstein:
1945547
EC Number:
201-704-2
MDL number:
MFCD00004047
UNSPSC Code:
41116107
PubChem Substance ID:
329755480
NACRES:
NA.24

grade

analytical standard

Quality Level

100

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

mp

180-183 °C (lit.)

application(s)

agriculture
environmental

format

neat

SMILES string

NC(=O)Cc1cccc2ccccc12

InChI

1S/C12H11NO/c13-12(14)8-10-6-3-5-9-4-1-2-7-11(9)10/h1-7H,8H2,(H2,13,14)

InChI key

XFNJVKMNNVCYEK-UHFFFAOYSA-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.

Legal Information

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

Signal Word

Danger

Hazard Statements

H302,H318,H361d,H412

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Repr. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCH7602
BCBW2057
SZBD120XV
SZBA109XV
SZBA109X

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Tsung-Rong Kuo et al.
Analytica chimica acta, 699(1), 81-86 (2011-06-28)
A simple technique for quantitative analysis of four urinary biomarkers, tryptophan (TRP), 5-hydroxytryptophan (5-HTP), 5-hydroxytryptamine (5-HT) and 5-hydroxyindole acetic acid (5-HIAA) of carcinoid tumors is developed using gold nanoparticles as the assisted matrix in surface-assisted laser desorption/ionization time-of-flight mass spectrometry
C Ravikumar et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 75(2), 859-866 (2010-01-06)
FT Raman and IR spectra of the biologically active molecule, 1-naphthalene acetamide (NA) have been recorded and analyzed. The equilibrium geometry, bonding features and harmonic vibrational wavenumbers of NA have been calculated with the help of B3LYP density functional theory
W P Cochrane et al.
Journal - Association of Official Analytical Chemists, 63(1), 145-148 (1980-01-01)
A simple, rapid, and accurate method has been developed for the determination of naphthalene-acetamide (NAAmide) residues in apples. After extraction with chloroform, separation is performed on an RP-8 high pressure liquid chromatographic column using acetonitrile-water (30 + 70) buffered to
Yoshitaka Arai et al.
Journal of plant research, 117(3), 191-198 (2004-03-26)
The activity of indole-3-acetamide (IAM) hydrolase from rice cells was enriched ca. 628-fold by gel filtration and anion exchange column chromatography. The molecular masses of the IAM hydrolase estimated by gel filtration and sodium dodecyl sulfate polyacrylamide gel electrophoresis were
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