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Key Documents

45451

Supelco

Dinobuton

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C14H18N2O7
CAS Number:
Molecular Weight:
326.30
Beilstein/REAXYS Number:
2065340
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
environmental

format

neat

SMILES string

CCC(C)c1cc(cc(c1OC(=O)OC(C)C)[N+]([O-])=O)[N+]([O-])=O

InChI

1S/C14H18N2O7/c1-5-9(4)11-6-10(15(18)19)7-12(16(20)21)13(11)23-14(17)22-8(2)3/h6-9H,5H2,1-4H3

InChI key

HDWLUGYOLUHEMN-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.

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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.

Legal Information

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

pictograms

Skull and crossbonesEnvironment

signalword

Danger

Hazard Classifications

Acute Tox. 2 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges


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F P Trinus et al.
Voprosy meditsinskoi khimii, 30(4), 48-50 (1984-07-01)
High affinity interactions between blood serum albumin and five substances of various chemical structure, exhibiting distinct physiological activity, were accompanied by alterations in the protein tertiary structure, while the albumin secondary structure was involved in conformational transformation after less effective
[The characteristics of extracting 4-methyl-2,6-dinitrophenol and 2-(1-methylpropyl)-4,6-dinitrophenol from aqueous solutions].
V K Shormanov et al.
Sudebno-meditsinskaia ekspertiza, 40(1), 36-38 (1997-01-01)
[Biological activity of soil microorganisms as an indicator of the toxic effects of acrex and metathione].
S A Ivashina
Gigiena i sanitariia, (12)(12), 65-66 (1983-12-01)
[Biological action of Acrex and substantiation of its maximum allowable concentration in atmospheric air].
R U Ubaĭdullaev et al.
Gigiena i sanitariia, (5)(5), 74-75 (1988-05-01)
[Data to substantiate the maximum permissible concentration of Acrex in soil].
A V Bolotnyĭ et al.
Gigiena i sanitariia, (11)(11), 77-78 (1985-11-01)

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