CAS 6161-87-1

2-(2,4,6-trichlorophenoxy)ethanol

Description:

2-(2,4,6-trichlorophenoxy)ethanol, with the CAS number 6161-87-1, is an organic compound characterized by its structure, which features a phenoxy group substituted with three chlorine atoms at the 2, 4, and 6 positions of the aromatic ring, linked to an ethanol moiety. This compound is typically a colorless to pale yellow liquid and is known for its use as a herbicide and in various agricultural applications due to its ability to inhibit plant growth. It exhibits moderate solubility in water and is more soluble in organic solvents, reflecting its amphiphilic nature. The presence of chlorine atoms enhances its biological activity and stability, but also raises concerns regarding environmental persistence and toxicity. Safety data indicates that it should be handled with care, as it may pose risks to human health and the environment. Proper storage and disposal practices are essential to mitigate potential hazards associated with this chemical.

Formula: C₈H₇Cl₃O₂

InChI: InChI=1/C8H7Cl3O2/c9-5-3-6(10)8(7(11)4-5)13-2-1-12/h3-4,12H,1-2H2

SMILES: C(COc1c(cc(cc1Cl)Cl)Cl)O

Synonyms:

• 2-(2,4,6-Trichloro-phenoxy)-ethanol
• Ethanol, 2-(2,4,6-Trichlorophenoxy)-
• 2-(2,4,6-Trichlorophenoxy)ethanol

2-(2,4,6-Trichlorophenoxy)ethanol

CAS: 6161-87-1

Formula: C₈H₇Cl₃O₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 241.4990

Ref: IN-DA00E9DF

2-(2,4,6-Trichlorophenoxy)ethanol

CAS: 6161-87-1

2-(2,4,6-Trichlorophenoxy)ethanol

Purity: 98%

Molecular weight: 241.5g/mol

Ref: 54-OR1063253

2-(2,4,6-Trichlorophenoxy)ethanol

CAS: 6161-87-1

Formula: C₈H₇Cl₃O₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 241.49

Ref: 10-F336976

2-(2,4,6-Trichlorophenoxy)ethanol

CAS: 6161-87-1

2-(2,4,6-Trichlorophenoxy)ethanol is a chlorinating agent that catalyzes the reaction of chlorine with hydroxyl groups to form hypochlorite. 2-(2,4,6-Trichlorophenoxy)ethanol can be used to produce chlorinated water or other disinfectants. It has been shown to have a weak estrogenic effect and has been found in the urine of animals treated with this compound. This chemical also binds to glucuronic acid and is excreted in the urine as a conjugate with glucuronide. The fixation of 2-(2,4,6-trichlorophenoxy)ethanol onto the imidazole ring of histidine residues can be inhibited by prochloraz and chloramine T.

Formula: C₈H₇Cl₃O₂

Purity: Min. 95%

Molecular weight: 241.5 g/mol

Ref: 3D-GAA16187