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Merck

45456

Supelco

Diphenylamin

PESTANAL®, analytical standard

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About This Item

Lineare Formel:
(C6H5)2NH
CAS-Nummer:
Molekulargewicht:
169.22
Beilstein:
508755
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
41116107
PubChem Substanz-ID:
NACRES:
NA.24

Qualität

analytical standard

Qualitätsniveau

Dampfdichte

5.82 (vs air)

Dampfdruck

1 mmHg ( 108 °C)

Produktlinie

PESTANAL®

Selbstzündungstemp.

1175 °F

Haltbarkeit

limited shelf life, expiry date on the label

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

bp

302 °C (lit.)

mp (Schmelzpunkt)

50-53 °C (lit.)

Anwendung(en)

agriculture
cleaning products
cosmetics
environmental
flavors and fragrances
food and beverages
personal care

Format

neat

SMILES String

N(c1ccccc1)c2ccccc2

InChI

1S/C12H11N/c1-3-7-11(8-4-1)13-12-9-5-2-6-10-12/h1-10,13H

InChIKey

DMBHHRLKUKUOEG-UHFFFAOYSA-N

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Allgemeine Beschreibung

Diphenylamine is an organic compound, used for post-harvest deterioration of apple and pear crops. It finds applications in rubber production, dyes, polymers, pesticides, pharmaceutical, lubricating oils and photography chemicals.

Anwendung

Diphenylamine may be used as an analytical reference standard for the quantification of the analyte in environmental samples and fruits using different analytical techniques.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Verpackung

abgefüllt unter Inertgas

Empfohlene Produkte

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Rechtliche Hinweise

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

Signalwort

Danger

Gefahreneinstufungen

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - STOT RE 2

Zielorgane

Kidney,Liver,spleen

Lagerklassenschlüssel

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

WGK

WGK 3

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges


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Kunden haben sich ebenfalls angesehen

A comparative study between PCR and PLS in simultaneous spectrophotometric determination of diphenylamine, aniline, and phenol: effect of wavelength selection
Hemmateenejad B, et al.
Spectrochimica Acta. Part A, Molecular and Biomolecular Spectroscopy, 67(2-4), 958-965 (2007)
Determination of ortho-phenylphenol, diphenyl and diphenylamine in apples and oranges using HPLC with fluorescence detection
Saad B, et al.
Food Chemistry, 84(2), 313-317 (2004)
Margot Van der Jeught et al.
Stem cells and development, 22(2), 296-306 (2012-07-13)
In embryonic stem cell culture, small molecules can be used to alter key signaling pathways to promote self-renewal and inhibit differentiation. In mice, small-molecule inhibition of both the FGF/MEK/Erk and the GSK3β pathways during preimplantation development suppresses hypoblast formation, and
M Francklin Philips et al.
Journal of hazardous materials, 237-238, 46-54 (2012-09-12)
Poly(diphenylamine-co-2-aminobenzonitrile) (P(DPA-co-2ABN)), a cyano group containing conducting polyaniline derivative, has been electrodeposited developed as the new material and utilized for the simultaneous electrochemical determination of trace levels of cadmium (Cd(2+)) and lead (Pb(2+)). P(DPA-co-2ABN) film preconcentrates effectively through cyano chelation
Walter J Jessen et al.
The Journal of clinical investigation, 123(1), 340-347 (2012-12-12)
Neurofibromatosis type 1 (NF1) patients develop benign neurofibromas and malignant peripheral nerve sheath tumors (MPNST). These incurable peripheral nerve tumors result from loss of NF1 tumor suppressor gene function, causing hyperactive Ras signaling. Activated Ras controls numerous downstream effectors, but

Protokolle

US EPA Method 8270 (Appendix IX): GC Analysis of Semivolatiles on Equity®-5 (30 m x 0.25 mm I.D., 0.50 μm)

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