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PS319

2,4-D isooctyl ester

analytical standard

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About This Item

CAS Number:
EC Number:
UNSPSC Code:
41116107

grade

analytical standard

packaging

ampule of 1000 mg

manufacturer/tradename

Chem Service, Inc. PS-319

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture

format

neat

InChI

1S/C16H22Cl2O3/c1-3-5-6-12(4-2)10-21-16(19)11-20-15-8-7-13(17)9-14(15)18/h7-9,12H,3-6,10-11H2,1-2H3

InChI key

QZSFJRIWRPJUOH-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

Exclamation markEnvironment

Signal Word

Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Skin Sens. 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

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Certificates of Analysis (COA)

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J Harville et al.
American Industrial Hygiene Association journal, 50(8), 438-446 (1989-08-01)
Tyvek (laminated saranax) and unsupported nitrile gloves gave protection from permeation against formulation concentrates and aqueous emulsions of Esteron 99 [isooctyl ester of (2,4-dichlorophenoxy)acetic acid] under conditions simulating extremes of field conditions. Neoprene gloves, whether unsupported or supported, lined or
[Effect of 2,4-D isooctylester on sperms in tail of epididymis and HSP70 expression of testis tissue in rats].
Guo-Yuan Chen et al.
Zhonghua lao dong wei sheng zhi ye bing za zhi = Zhonghua laodong weisheng zhiyebing zazhi = Chinese journal of industrial hygiene and occupational diseases, 22(4), 281-282 (2004-09-10)
Congyun Liu et al.
Environmental monitoring and assessment, 184(7), 4247-4251 (2011-08-05)
A simple analytical method was developed to determine the 2,4-D isooctyl ester residue in wheat and soil by gas chromatography coupled with electron capture detector. Using the method, the dissipation and residue of 2,4-D isooctyl ester in wheat field was
R P Moody et al.
Journal of toxicology and environmental health, 29(3), 237-245 (1990-01-01)
Dermal absorption of the 14C-ring-labeled phenoxy herbicides 2,4-D [(2,4-dichlorophenoxy)acetic acid], 2,4-D amine (2,4-dichlorophenoxyacetic acid dimethylamine), 2,4-D isooctyl (2,4-dichlorophenoxyacetic acid isooctyl ester), and 2,4,5-T amine (2,4,5-trichlorophenoxyacetic acid trimethylamine) was examined following topical applications of the herbicides to the back of rabbits
Acute toxicity of four phenoxy herbicides to aquatic organisms.
H C Alexander et al.
Bulletin of environmental contamination and toxicology, 35(3), 314-321 (1985-09-01)

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