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Merck
CN

36587

Supelco

Propazine solution

100 μg/mL in methanol, PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C9H16ClN5
CAS Number:
139-40-2
Molecular Weight:
229.71
Beilstein:
747081
EC Number:
200-659-6
MDL number:
MFCD00047341
UNSPSC Code:
41116107
PubChem Substance ID:
329755410
NACRES:
NA.24

Key Documents

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grade

analytical standard

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

concentration

100 μg/mL in methanol

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
cleaning products
cosmetics
food and beverages
personal care

format

single component solution

storage temp.

2-8°C

SMILES string

CC(C)Nc1nc(Cl)nc(NC(C)C)n1

InChI

1S/C9H16ClN5/c1-5(2)11-8-13-7(10)14-9(15-8)12-6(3)4/h5-6H,1-4H3,(H2,11,12,13,14,15)

InChI key

WJNRPILHGGKWCK-UHFFFAOYSA-N

General description

Standard for Supelco MIP SPE cartridges. For more information request Supelco Literature T407075, T706023

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 Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Flam. Liq. 2 - STOT SE 1

Target Organs

Eyes

Storage Class Code

3 - Flammable liquids

WGK

WGK 2

Flash Point(F)

51.8 °F

Flash Point(C)

11 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

危险化学品
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Certificates of Analysis (COA)

Lot/Batch Number
BCBS2259V

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C Cacho et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 802(2), 347-353 (2004-03-17)
In this paper, the Langmuir-Freundlich isotherm (LF) is used to characterise a propazine-imprinted polymer obtained by precipitation polymerisation (MIP-P). Different rebinding studies were carried out allowing to explain the different interactions taking place between the molecularly imprinted polymer and six
H Jiang et al.
Environmental science & technology, 40(11), 3609-3616 (2006-06-22)
Atrazine, simazine, and propazine and their major chlorinated degradates (deethylatrazine, deisopropylatrazine, and didealkylatrazine) are considered as a group to be endocrine-disrupting chemicals by the U.S. Environmental Protection Agency. On this basis, regulatory action levels are currently under consideration for the
C Cacho et al.
Analytical and bioanalytical chemistry, 376(4), 491-496 (2003-05-10)
An analytical methodology based on a molecularly imprinted solid-phase extraction (MISPE) procedure was developed for the determination of several triazines (atrazine, simazine, desethylatrazine (DEA), desisopropylatrazine (DIA), and propazine) in vegetable samples. A methacrylic acid-based imprinted polymer was prepared by precipitation
J T Sanderson et al.
Environmental health perspectives, 109(10), 1027-1031 (2001-10-25)
We investigated a potential mechanism for the estrogenic properties of three chloro-s-triazine herbicides and six metabolites in vitro in several cell systems. We determined effects on human aromatase (CYP19), the enzyme that converts androgens to estrogens, in H295R (adrenocortical carcinoma)
Luciana B O Dos Santos et al.
Journal of separation science, 32(4), 494-500 (2009-02-13)
This paper describes the development of a sequential injection chromatography (SIC) procedure for separation and quantification of the herbicides simazine, atrazine, and propazine exploring the low backpressure of a 2.5 cm long monolithic C(18) column. The separation of the three
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