103896-91-9

Basic information

• Product Name: (2,5-DIMETHYL-PHENOXY)-ACETIC ACID HYDRAZIDE
• Synonyms: 2-(2,5-dimethylphenoxy)acetohydrazide(SALTDATA: FREE);ARONIS001015;Oprea1_180451;ST5211127;ZINC02581477
• CAS NO: 103896-91-9
• Molecular Formula: C₁₀H₁₄N₂O₂
• Molecular Weight: 194.24
• Mol File: 103896-91-9.mol

Chemical Properties

• Boiling Point: 406.5°Cat760mmHg
• Flash Point: 199.6°C
• Appearance: /
• Density: 1.128g/cm³
• Vapor Pressure: 8.12E-07mmHg at 25°C
• Refractive Index: 1.544
• CAS DataBase Reference: (2,5-DIMETHYL-PHENOXY)-ACETIC ACID HYDRAZIDE(CAS DataBase Reference)
• NIST Chemistry Reference: (2,5-DIMETHYL-PHENOXY)-ACETIC ACID HYDRAZIDE(103896-91-9)
• EPA Substance Registry System: (2,5-DIMETHYL-PHENOXY)-ACETIC ACID HYDRAZIDE(103896-91-9)

Safety Data

• Hazardous Substances Data: 103896-91-9(Hazardous Substances Data)

Usage

Uses

Used in Agricultural Industry:
(2,5-DIMETHYL-PHENOXY)-ACETIC ACID HYDRAZIDE is used as a herbicide for controlling and eliminating unwanted plant growth. It is applied for its ability to interfere with the plant's hormonal system, effectively inhibiting growth and leading to the plant's death. This application is particularly useful in managing weed populations and maintaining the health and productivity of crops.
Used as a Plant Growth Regulator:
In addition to its herbicidal properties, (2,5-DIMETHYL-PHENOXY)-ACETIC ACID HYDRAZIDE is also utilized as a plant growth regulator. It helps in managing the growth patterns of plants, which can be beneficial in various agricultural practices where controlling plant size or growth rate is necessary for optimal crop yield and quality.
Safety and Environmental Considerations:
(2,5-DIMETHYL-PHENOXY)-ACETIC ACID HYDRAZIDE is used with the understanding that it has low toxicity to mammals, making it a safer alternative for use in environments where human and animal safety is a concern. However, it is imperative to handle, store, and apply this chemical according to the manufacturer's recommendations to minimize any potential risks to the environment, non-target organisms, and human health. Compliance with safety instructions and regulations is essential to ensure the responsible and effective use of this chemical compound.

InChI:InChI=1/C10H14N2O2/c1-7-3-4-8(2)9(5-7)14-6-10(13)12-11/h3-5H,6,11H2,1-2H3,(H,12,13)

Upstream product

• 95-87-4 2,5-Dimethylphenol 

Downstream Products

• 125299-04-9 (2,5-Dimethyl-phenoxy)-acetic acid [2-oxo-1,2-dihydro-indol-(3Z)-ylidene]-hydrazide 
• 103896-75-9 C₁₇H₁₈ClN₃O₂S 
• 103896-74-8 C₁₇H₁₈ClN₃O₂S 
• 103896-86-2 [4-(3-Chloro-phenyl)-5-(2,5-dimethyl-phenoxymethyl)-4H-[1,2,4]triazol-3-ylsulfanyl]-acetic acid 
• 103896-87-3 [4-(4-Chloro-phenyl)-5-(2,5-dimethyl-phenoxymethyl)-4H-[1,2,4]triazol-3-ylsulfanyl]-acetic acid 
• 103896-85-1 [5-(2,5-Dimethyl-phenoxymethyl)-4-phenyl-4H-[1,2,4]triazol-3-ylsulfanyl]-acetic acid 
• 103896-80-6 4-(3-Chloro-phenyl)-5-(2,5-dimethyl-phenoxymethyl)-4H-[1,2,4]triazole-3-thiol 
• 103896-81-7 4-(4-Chloro-phenyl)-5-(2,5-dimethyl-phenoxymethyl)-4H-[1,2,4]triazole-3-thiol 
• 103896-79-3 5-(2,5-Dimethyl-phenoxymethyl)-4-phenyl-4H-[1,2,4]triazole-3-thiol 
• 103896-73-7 1-(2,5-dimethylphenoxymethyl)-4-phenylthiosemicarbazide 
• 125299-14-1 C₂₀H₁₉N₃O₄S 

Relevant articles and documents

Synthesis and Herbicidal Activity of Some Novel Pyrazole Derivatives

Some novel pyrazole derivatives were designed and synthesized through multi-step reactions from substituted phenol as starting material. Their structures were confirmed by 1H NMR, FTIR, MS and elemental analysis. All these compounds were evaluated their herbicidal activity. The preliminary bioassay results indicated that some of title compounds displayed moderate herbicidal activity at 200 μg/mL. Among them, compounds 4-chloro-N'-(2-(2,5-dimethyl-phenoxy) acetyl)-3-ethyl-1-methyl-1H-pyrazole-5-carbohydrazide, 4-chloro-N'-(2-(2,4-dichlorophenoxy)acetyl)- 3-ethyl-1-methyl-1H-pyrazole-5-carbohydrazide, 4-chloro-3-ethyl-1-methyl-N'-(2-(m-tolyloxy) acetyl)-1H-pyrazole-5-carbohydrazide and 4-chloro-3-ethyl-1-methyl-N'-(2-(3-nitrophenoxy)acetyl)- 1H-pyrazole-5-car-bohydrazide possessed 95%, 100%, 95% and 95% inhibition against Brassica campestris respectively. In the further bioassay, the compound 6l exhibited excellent herbicidal activity either monocotyledon or dicotyledon plant at 150 g/ha.