13335-73-4

Basic information

• Product Name: 3,4-DIMETHYLPHENOXYACETIC ACID
• Synonyms: OTAVA-BB BB7210540030;3,4-DIMETHYLPHENOXYACETIC ACID;AKOS BC-2698;AKOS BBS-00006524;AKOS BBB/236;3,4-xylyloxyacetic acid;3,4-Dimethylphenoxyacetic acid 97%;2-(3,4-dimethylphenoxy)ethanoic acid
• CAS NO: 13335-73-4
• Molecular Formula: C₁₀H₁₂O₃
• Molecular Weight: 180.2
• EINECS: 236-386-4
• Product Categories: Phenoxyacetic Acids and Alcohols (substituted)
• Mol File: 13335-73-4.mol
• Article Data: 6

Chemical Properties

• Melting Point: 164-166°C
• Boiling Point: 323.5 °C at 760 mmHg
• Flash Point: 128.2 °C
• Appearance: /
• Density: 1.146 g/cm³
• Vapor Pressure: 0.000107mmHg at 25°C
• Refractive Index: 1.533
• BRN: 2558866
• CAS DataBase Reference: 3,4-DIMETHYLPHENOXYACETIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 3,4-DIMETHYLPHENOXYACETIC ACID(13335-73-4)
• EPA Substance Registry System: 3,4-DIMETHYLPHENOXYACETIC ACID(13335-73-4)

Safety Data

• Hazard Codes: Xi,Xn
• Statements: 36/37/38-22
• Safety Statements: 26-37
• HazardClass: IRRITANT
• Hazardous Substances Data: 13335-73-4(Hazardous Substances Data)

Usage

General Description

3,4-DIMETHYLPHENOXYACETIC ACID is a chemical compound consisting of a phenyl ring with two methyl groups attached at the 3 and 4 positions, as well as a phenoxy group and an acetic acid moiety. It is commonly used as a herbicide and plant growth regulator, often applied to crops such as wheat, barley, and grapes to control the growth of weeds and increase the yield of the desired plants. The compound functions by mimicking the plant hormone auxin, disrupting normal plant growth and development processes. It is typically applied as a foliar spray or as a pre-harvest treatment, and has potential implications for human health and the environment due to its long persistence in soil and water.

InChI:InChI=1/C10H12O3/c1-7-3-4-9(5-8(7)2)13-6-10(11)12/h3-5H,6H2,1-2H3,(H,11,12)

Upstream product

• 95-65-8 3,4-Dimethylphenol 
• 79-11-8 chloroacetic acid 
• 79-08-3 bromoacetic acid 
• 192634-75-6 ethyl [(3,4-dimethylphenyl)oxy]acetate 
• 95450-81-0 (3,4-dimethyl-phenoxy)-acetic acid methyl ester 

Downstream Products

• 34279-10-2 3-[1-(3,4-Dimethyl-phenoxy)-meth-(Z)-ylidene]-3H-isobenzofuran-1-one 
• 1107603-71-3 C₂₅H₃₇NO₅ 
• 1107603-72-4 C₂₅H₃₇NO₅ 
• 123216-99-9 5-{[(3,4-dimethylphenyl)oxy]methyl}-1,3,4-thiadiazol-2-amine 
• 95450-81-0 (3,4-dimethyl-phenoxy)-acetic acid methyl ester 
• 82326-46-3 2-(3,4-Dimethyl-phenoxymethyl)-1H-benzoimidazole 
• 899270-46-3 2-(3,4-dimethylphenoxy)-N-(4-methylthiazol-2-yl)acetamide 
• 1440434-94-5 2-(3,4-dimethylphenoxy)-N-(4-(3-fluorophenyl)thiazol-2-yl)acetamide 
• 1440434-98-9 N-(4-(3-chlorophenyl)thiazol-2-yl)-2-(3,4-dimethylphenoxy)acetamide 

Relevant articles and documents

1,3,4-Thiadiazol-2-amine Derivatives as Urotensin-II Receptor (UT) Antagonists

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THIADIAZOLE DERIVATIVES, INHIBITORS OF STEAROYL-COA DESATURASE

The present invention relates to substituted thiadiazole compounds of the formula (I) and pharmaceutically acceptable salts thereof, to pharmaceutical compositions containing them and their use in medicine. In particular, the invention relates to compounds for modulating SCD activity.

Design, Synthesis, and Testing of Potential Antisickling Agents. 4. Structure-Activity Relationships of Benzyloxy and Phenoxy Acids

In this paper we further establish the activity of two classes of small molecules, benzyloxy and phenoxy acids, as potent inhibitors of hemoglobin S (HbS) gelation.Structural modifications with a large number of each class confirm our earlier work that the highest activity is observed with compounds that contain dihalogenated aromatic rings with attached polar side chains.We have also found a halogenated aromatic malonic acid derivative to be quite active.Compounds reported in this paper are compared with other antigelling agents studied in our laboratory.Comments are made concerning the antigelling activity and binding sites of four derivatives and their effect on the allosteric mechanism of hemoglobin (Hb) function.