N-Cyclopropyl-2,4,6-triamino-1,3,5-triazin

Name: <I>N</I>-Cyclopropyl-2,4,6-triamino-1,3,5-triazin
Brand: ALDRICH
Price: 307 EUR

97%

Synonym(e):

N-Cyclopropyl-1,3,5-triazin-2,4,6-triamin, Cyromazin

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Über diesen Artikel

Empirische Formel (Hill-System):

C₆H₁₀N₆

CAS-Nummer:

66215-27-8

Molekulargewicht:

166.18

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24879213

EC Number:

266-257-8

Beilstein/REAXYS Number:

882879

MDL number:

MFCD00078650

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Produktname

N-Cyclopropyl-2,4,6-triamino-1,3,5-triazin, 97%

InChI key

LVQDKIWDGQRHTE-UHFFFAOYSA-N

InChI

1S/C6H10N6/c7-4-10-5(8)12-6(11-4)9-3-1-2-3/h3H,1-2H2,(H5,7,8,9,10,11,12)

SMILES string

Nc1nc(N)nc(NC2CC2)n1

assay

97%

mp

223-227 °C (lit.)

Quality Level

100

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Dieser Artikel	93101	C33301	D23408
Sigma-Aldrich 551295 N-Cyclopropyl-2,4,6-triamino-1,3,5-triazin	Supelco 93101 Cyromazin-(cyclopropyl-2,2,3,3-d₄)	Sigma-Aldrich C33301 Atrazin-desethyl-desisopropyl	Sigma-Aldrich D23408 2,4-Diamino-6-Phenyl-1,3,5-Triazin
assay 97%	assay ≥98.0% (HPLC)	assay 95%	assay 97%
Quality Level 100	Quality Level 100	Quality Level 200	Quality Level 100
mp 223-227 °C (lit.)	mp -	mp >320 °C (lit.)	mp 219-221 °C (lit.)

General description

N-Cyclopropyl-2,4,6-triamino-1,3,5-triazine, also known as cyromazine, is an insect growth regulator(IGR) that is commonly used as an insecticide. It undergoes metabolism in plants and animals to form melamine.[1] Surface-enhanced Raman scattering (SERS) spectroscopic study indicates that it interacts with the surface of silver colloid through the lone pair on nitrogen.[2]

Hazard Classifications

Aquatic Chronic 2

Lagerklasse

11 - Combustible Solids

wgk

WGK 2

flash_point_f

212.0 °F - closed cup

flash_point_c

100 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

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Raman and surface-enhanced Raman study of insecticide cyromazine.

Mukherjee K, et al.

Vibrational Spectroscopy, 25(1), 91-99 (2001)

[Adsorption of cyromazine on five typical soils in China].

Ling-li Tang et al.

Huan jing ke xue= Huanjing kexue, 30(10), 3072-3076 (2009-12-09)

Batch equilibrium experiments were used to reveal cyromazine adsorption on five kinds of soils, namely Ali-Perudic Ferrosols collected from Yingtan of Jiangxi, Udic Argosols collected from Nanjing and Gleyic-Stagnic Anthrosols collected from Changshu of Jiangsu, Ustic Cambosols collected from Fengqiu

Determination of residues of cyromazine and its metabolite, melamine, in animal-derived food by gas chromatography-mass spectrometry with derivatization.

Xinle Zhu et al.

Journal of agricultural and food chemistry, 57(23), 11075-11080 (2009-11-11)

A gas chromatography-mass spectrometric (GC-MS) method was established for the determination of cyromazine and its metabolite, melamine, in animal-derived food. Chicken and tilapia muscle samples were spiked with (15)N(3)-melamine, extracted with an acidic acetonitrile/water solution, and defatted with dichloromethane. Egg

Putative polymerase chain reaction markers for insecticide resistance in the leafminer Liriomyza trifolii (Diptera: Agromyzidae) to cyromazine and abamectin.

Scott Ferguson et al.

Journal of economic entomology, 103(6), 2197-2203 (2011-02-12)

In this study, random amplified polymorphic DNA polymerase chain reaction (RAPD-PCR) was used to identify polymorphic genomic DNA that would discriminate among cyromazine-resistant, abamectin-resistant, and susceptible Liriomyza trifolii (Burgess) (Diptera: Agromyzidae) leafminers. Using a reference strain that was susceptible to

Efficacy of cyromazine to control immature stable flies (Diptera: Muscidae) developing in winter hay feeding sites.

D B Taylor et al.

Journal of economic entomology, 105(2), 726-731 (2012-05-23)

Hay mixed with manure and urine residues at sites where hay has been provided as supplemental winter feed for cattle provide an excellent substrate for the development of immature stable flies, Stomoxys calcitrans (L.). Such sites are primary sources of

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N-Cyclopropyl-2,4,6-triamino-1,3,5-triazin