Skip to Content
Merck
CN
All Photos(1)

Key Documents

View All Documentation

Safety Information

45420

Supelco

2,4-DB

PESTANAL®, analytical standard

Synonym(s):

4-(2,4-Dichlorophenoxy)butyric acid, 2,4-DB

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
Cl2C6H3O(CH2)3CO2H
CAS Number:
94-82-6
Molecular Weight:
249.09
Beilstein:
1976809
EC Number:
202-366-9
MDL number:
MFCD00002819
UNSPSC Code:
12352209
PubChem Substance ID:
329756717
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

mp

118-120 °C (lit.)

application(s)

agriculture
environmental

format

neat

SMILES string

COc1ccc(cc1OC)[C@H](CC(O)=O)NC(=O)OC(C)(C)C
OC(=O)CCCOc1ccc(Cl)cc1Cl

InChI

1S/C10H10Cl2O3/c11-7-3-4-9(8(12)6-7)15-5-1-2-10(13)14/h3-4,6H,1-2,5H2,(H,13,14)

InChI key

YIVXMZJTEQBPQO-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

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

Not finding the right product?  

Try our Product Selector Tool.

Pictograms

Exclamation markEnvironment
GHS07,GHS09

Signal Word

Warning

Hazard Statements

H302,H411

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Regulatory Information

农药列管产品

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCBZ3299
BCBW5710

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Tuansheng Shi et al.
Journal of agricultural and food chemistry, 53(6), 2207-2212 (2005-03-17)
Effects of diethyl suberate (DESU), diethyl sebacate (DES), dibutyl suberate (DBSU), dibutyl sebacate (DBS), and tributyl phosphate (TBP) on diffusion of 14C-2,4-dichlorophenoxy butyric acid (2,4-DB) across cuticular membranes (CM) was studied. Astomatous CM were isolated enzymatically from Stephanotis floribunda Brongn.
Andrew A G Wiszniewski et al.
Plant molecular biology, 69(5), 503-515 (2008-12-02)
Indole-3-butyric acid (IBA) and 2,4-dichlorophenoxybutyric acid (2,4-DB) are metabolised by peroxisomal beta-oxidation to active auxins that inhibit root growth. We screened Arabidopsis mutants for resistance to IBA and 2,4-DB and identified two new 2,4-DB resistant mutants. The mutant genes encode
Mohd Zobir Bin Hussein et al.
Journal of nanoscience and nanotechnology, 9(3), 2140-2147 (2009-05-14)
Hybridization of beneficial organic guest with inorganic host affords scientists an opportunity to synthesize various combinations of new organic-inorganic nanohybrids with various potential applications, especially for controlled delivery of beneficial agent and storage. A new layered organic-inorganic nanohybrid material containing
Virginia Cuadrado et al.
International journal of systematic and evolutionary microbiology, 60(Pt 11), 2606-2612 (2009-12-22)
A bacterial consortium able to degrade the herbicide 4-(2,4-dichlorophenoxy) butyric acid (2,4-DB) was obtained from an agricultural soil of the Argentinean Humid Pampa region which has a history of long-term herbicide use. Four bacterial strains were isolated from the consortium
Eva Simánová et al.
Pest management science, 61(4), 383-389 (2005-03-08)
Equilibrium sorption of n-alkyl esters (dimethyl suberate, diethyl suberate, diethyl sebacate, dibutyl suberate and dibutyl sebacate) and monodisperse alcohol ethoxylates (diethylene glycol, tetraethylene glycol, pentaethylene glycol, hexaethylene glycol and octaethylene glycol monododecyl ether) between the reconstituted cuticular waxes of Stephanotis
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service