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45381

Supelco

Chlorofenprop-methyl

PESTANAL®, analytical standard

Synonym(s):

Chlorophenprop-methyl

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About This Item

Empirical Formula (Hill Notation):
C10H10Cl2O2
CAS Number:
14437-17-3
Molecular Weight:
233.09
Beilstein:
2331933
EC Number:
238-413-5
MDL number:
MFCD00055268
UNSPSC Code:
41116107
PubChem Substance ID:
329756688
NACRES:
NA.24

grade

analytical standard

Quality Level

100

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

COC(=O)C(Cl)Cc1ccc(Cl)cc1

InChI

1S/C10H10Cl2O2/c1-14-10(13)9(12)6-7-2-4-8(11)5-3-7/h2-5,9H,6H2,1H3

InChI key

YJKIALIXRCSISK-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.

Legal Information

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

Pictograms

Skull and crossbonesEnvironment
GHS06,GHS09

Signal Word

Danger

Hazard Statements

H302,H311,H410

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1

Storage Class Code

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

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

45381S-50MG:
45381-50MG:
45381-250MG:
45381-VAR:
45381-1EA:
45381-BULK:

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Certificates of Analysis (COA)

Lot/Batch Number
BCCF9767
BCBW2041
BCBS8723V
SZBD022XV
SZB8017XV

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Istvan Jablonkai
Pest management science, 59(4), 443-450 (2003-04-19)
The relationship between S- and N-alkylating reactivity and herbicidal activity within a series of chloroacetamides, including several commercial herbicides and newly synthesised analogues was studied. The S-alkylating reactivity of selected chloroacetamides, as well as those of atrazine and chlorfenprop-methyl, was

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