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Safety Information

PS355

Propachlor

analytical standard

Synonym(s):

2-Chloro-N-isopropylacetanilide

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About This Item

Empirical Formula (Hill Notation):
C11H14ClNO
CAS Number:
1918-16-7
Molecular Weight:
211.69
Beilstein:
2103903
EC Number:
217-638-2
MDL number:
MFCD00078731
UNSPSC Code:
41116107
PubChem Substance ID:
24899193

grade

analytical standard

packaging

ampule of 250 mg

manufacturer/tradename

Chem Service, Inc. PS-355

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
environmental

format

neat

SMILES string

CC(C)N(C(=O)CCl)c1ccccc1

InChI

1S/C11H14ClNO/c1-9(2)13(11(14)8-12)10-6-4-3-5-7-10/h3-7,9H,8H2,1-2H3

InChI key

MFOUDYKPLGXPGO-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.

Pictograms

Skull and crossbonesEnvironment
GHS06,GHS09

Signal Word

Danger

Hazard Statements

H302,H311,H317,H319,H410

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - Skin Sens. 1

Storage Class Code

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

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

农药列管产品
危险化学品

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Certificates of Analysis (COA)

Lot/Batch Number

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Sheng Tai et al.
Molecular cancer therapeutics, 11(6), 1320-1331 (2012-04-12)
PI3K/AKT/mTOR pathway plays a key role in the tumorigenesis of many human cancers including prostate cancer. However, inhibitors of this pathway, such as Rad001, have not shown therapeutic efficacy as a single agent. Through a high-throughput screen of 5,000 widely
A R Loch et al.
Environmental science & technology, 36(19), 4065-4073 (2002-10-17)
Reactions of bisulfide and polysulfides with alachlor, propachlor, and metolachlor were examined in aqueous solution to investigate the role reduced sulfur species could play in effecting abiotic transformations of chloroacetanilide herbicides. Experiments at 25 degrees C demonstrated that reactions were
M B Genter et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 47(6), 1051-1057 (2009-05-09)
Alachlor and butachlor are chloracetanilide herbicides that induce olfactory tumors in rats, whereas propachlor does not. The mechanism by which alachlor induces tumors is distinct from many other nasal carcinogens, in that alachlor induces a gradual de-differentiation of the olfactory
K L Davison et al.
Xenobiotica; the fate of foreign compounds in biological systems, 24(10), 1003-1012 (1994-10-01)
1. 14C-labelled propachlor, alachlor, butachlor, metolachlor, methoxypropachlor and some of their mercapturic acid pathway metabolites (MAP) were given to rat either by gavage or by perfusion into a renal artery. MAP metabolites were isolated from bile and urine. 2. Rat
Ioannis K Konstantinou et al.
Water research, 36(11), 2733-2742 (2002-07-31)
The light-induced degradation of propachlor (2-chloro-N-isopropylacetanilide) under simulated solar irradiation has been investigated in aqueous solutions containing TiO2 suspensions as photocatalysts. The study focuses on the identification of possible intermediate products and the determination of inorganic ions formed during the
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