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36761

Supelco

3-Chloro-4-methylaniline

PESTANAL®, analytical standard

Sinonimo/i:

3-Chloro-p-toluidine, 4-Amino-2-chlorotoluene

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About This Item

Formula condensata:
ClC6H3(CH3)NH2
Numero CAS:
95-74-9
Peso molecolare:
141.60
Beilstein:
636511
Numero CE:
202-446-3
Numero MDL:
MFCD00007773
Codice UNSPSC:
41116107
ID PubChem:
329755498

Grado

analytical standard

Nome Commerciale

PESTANAL®

Durata

limited shelf life, expiry date on the label

tecniche

HPLC: suitable
gas chromatography (GC): suitable

Indice di rifrazione

n20/D 1.584 (lit.)

P. eboll.

237-238 °C (lit.)

Punto di fusione

24-25 °C (lit.)

applicazioni

agriculture
environmental

Formato

neat

Stringa SMILE

Cc1ccc(N)cc1Cl

InChI

1S/C7H8ClN/c1-5-2-3-6(9)4-7(5)8/h2-4H,9H2,1H3
RQKFYFNZSHWXAW-UHFFFAOYSA-N

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Applicazioni

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Note legali

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

Pittogrammi

Skull and crossbonesEnvironment
GHS06,GHS09

Avvertenze

Danger

Indicazioni di pericolo

H301 + H311,H315,H317,H319,H410

Classi di pericolo

Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1

Codice della classe di stoccaggio

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

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

212.0 °F - closed cup

Punto d’infiammabilità (°C)

100 °C - closed cup

Dispositivi di protezione individuale

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

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Certificati d'analisi (COA)

Lot/Batch Number
SZBF118XV
SZBB207XV
SZB6313XV
SZE6313X
6313X

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Randal S Stahl et al.
Journal of agricultural and food chemistry, 50(4), 732-738 (2002-02-07)
A method using a deuterated surrogate of the avicide 3-chloro-p-toluidine hydrochloride (CPTH) was developed to quantify the CPTH residues in the gastrointestinal (GI) tract and breast muscle tissues in birds collected in CPTH-baited sunflower and rice fields. This method increased
Angshuman Bagchi et al.
Computational biology and chemistry, 30(3), 227-232 (2006-05-25)
Microbial redox reactions involving inorganic sulfur compounds in the environment are one of the major reactions of the global sulfur cycle. These reactions are mediated by phylogenetically diverse prokaryotes containing the sulfur oxidizing gene cluster (sox). The sox gene cluster
David A Goldade et al.
Journal of agricultural and food chemistry, 52(26), 8074-8080 (2004-12-23)
Ring-labeled [14C]-3-chloro-4-methylaniline hydrochloride (250 microg per bird) was delivered to 21 red-winged blackbirds (Agelaius phoeniceus) and 21 dark-eyed juncos (Junco hyemalis) via oral gavage, and the distribution and excretion of radioactivity were determined at 15 and 30 min and 1
J C Hurley et al.
Journal of agricultural and food chemistry, 47(7), 2904-2907 (1999-12-20)
Stabilization of the avicide 3-chloro-p-toluidine (CPTH) on rice baits by pseudo latex polymeric coating and beta-cyclodextin inclusion was investigated. When CPTH-treated rice baits were exposed to sunlight, the CPTH formed colored compounds, which exacerbated problems with bait acceptance and efficacy.
[Method of determining p-nitrotoluene, 2-chloro-4-nitrotoluene and 3-chloro-4-methylaniline in the air].
I I Pilenkova et al.
Gigiena truda i professional'nye zabolevaniia, (1)(1), 43-44 (1980-01-01)
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