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4-Chloro-3,5-dimethylphenol

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Name

4-Chloro-3,5-dimethylphenol

EINECS 201-793-8
CAS No. 88-04-0 Density 1.183 g/cm3
PSA 20.23000 LogP 2.66240
Solubility 0.3 g/L (20 °C) in water Melting Point 114-116 °C(lit.)
Formula C8H9ClO Boiling Point 246 °C at 760 mmHg
Molecular Weight 156.612 Flash Point 105.9 °C
Transport Information UN 3077 9/PG 3 Appearance white or cream crystalline powder with a characteristic odour
Safety 24-37 Risk Codes 22-36/38-43
Molecular Structure Molecular Structure of 88-04-0 (4-Chloro-3,5-dimethylphenol) Hazard Symbols HarmfulXn, IrritantXi
Synonyms

3,5-Xylenol,4-chloro- (6CI,8CI);2-Chloro-5-hydroxy-1,3-dimethylbenzene;2-Chloro-5-hydroxy-m-xylene;4-Chloro-3,5-Xylenol;4-Chloro-3,5-dimethylphenol;4-Chloro-5,3-dimethylphenol;4-Chloro-m-xylenol;Benzytol;Camel;Camel(pesticide);Chloroxylenol;Desson;Dettol;Dettol (biocide);Ecotru;Espadol;Husept Extra;NSC 4971;Nipacide PX;Ottasept Extra;PCMX;Parametaxylenol;RBA 777;p-Chloro-3,5-xylenol;p-Chloro-m-Xylenol;

Article Data 34

4-Chloro-3,5-dimethylphenol Synthetic route

108-68-9

3,5-Dimethylphenol

88-04-0

4-Chloro-3,5-dimethylphenol

Conditions
ConditionsYield
With N-chloro-N-(benzenesulfonyl)benzenesulfonamide In acetonitrile at 20 - 25℃; for 0.166667h; Green chemistry;98.9%
With hydrogenchloride; copper(II) choride dihydrate; oxygen; sodium chloride In 1,2-dichloro-ethane at 80℃; under 3750.38 Torr; Temperature; Solvent; Reagent/catalyst; Autoclave;97.2%
With iron(III) chloride; N-chloro-succinimide; 1-butyl-3-methylimidazolium trifluoromethanesulfonimide In tetrahydrofuran at 60℃; for 12h; Inert atmosphere; regioselective reaction;76%
6981-15-3

4-chloro-3,5-dimethylanisole

88-04-0

4-Chloro-3,5-dimethylphenol

Conditions
ConditionsYield
Kaninchen-Organismus;
With boron tribromide In dichloromethane at 0℃; for 2h;
22012-58-4

4-chloro-3, 5, dimethyl phenyl acetate

88-04-0

4-Chloro-3,5-dimethylphenol

Conditions
ConditionsYield
Kaninchen-Organismus;
108-68-9

3,5-Dimethylphenol

A

88-04-0

4-Chloro-3,5-dimethylphenol

B

5538-41-0

o-chloro-m-xylenol

Conditions
ConditionsYield
With sulfuryl dichloride; chloroform
With iron(III) chloride; 1,2-dithiacyclooctane; sulfuryl dichloride In dichloromethane at 20℃; for 4h; Reagent/catalyst; regioselective reaction;A 89 %Chromat.
B 7.6 %Chromat.
With 1,3-dichloro-5,5-dimethylhydantoin; diisopropylamine hydrochloride In toluene at 0℃; for 4h; Darkness; Overall yield = 86 %; regioselective reaction;

4-chloro-3,5-dimethylphenyl phosphate monoester

88-04-0

4-Chloro-3,5-dimethylphenol

Conditions
ConditionsYield
With hydrogenchloride at 98℃; Kinetics; Mechanism; Thermodynamic data; E(activ.), ΔS(excit.);

N,N,N',N'-Tetramethyl-acridine-3,6-diamine; compound with 4-chloro-3,5-dimethyl-phenol

A

88-04-0

4-Chloro-3,5-dimethylphenol

B

494-38-2

acridine orange

Conditions
ConditionsYield
In benzonitrile at 25℃; Equilibrium constant; ionic strength 0.1 M;

N,N,N',N'-Tetramethyl-acridine-3,6-diamine; compound with 4-chloro-3,5-dimethyl-phenol

A

88-04-0

4-Chloro-3,5-dimethylphenol

B

494-38-2

acridine orange

Conditions
ConditionsYield
In benzonitrile at 25℃; Equilibrium constant; ionic strength 0.1 M;
108-68-9

3,5-Dimethylphenol

A

88-04-0

4-Chloro-3,5-dimethylphenol

B

133-53-9

2,4-dichloro-3,5-dimethylphenol

Conditions
ConditionsYield
With N-chlorotriethylammonium chloride In trifluoroacetic acid Ambient temperature; Yield given. Yields of byproduct given;
7782-50-5

chlorine

64-19-7

acetic acid

108-68-9

3,5-Dimethylphenol

88-04-0

4-Chloro-3,5-dimethylphenol

67-66-3

chloroform

108-68-9

3,5-Dimethylphenol

sulfuryl chloride (1 mol)

sulfuryl chloride (1 mol)

A

88-04-0

4-Chloro-3,5-dimethylphenol

B

5538-41-0

o-chloro-m-xylenol

4-Chloro-3,5-dimethylphenol Specification

The 4-Chloro-3,5-xylenol is an organic compound with the formula C8H9ClO. The IUPAC name of this chemical is 4-chloro-3,5-dimethylphenol. With the CAS registry number 88-04-0, it is also named as 2-Chloro-5-hydroxy-1,3-dimethylbenzene. The product's category is Categories: Phenoles and Thiophenoles. Besides, it is a white or cream crystalline powder with a characteristic odour, which should be stored in a cool, dry place at temperature of 2 - 8 °C. It used as Antiseptic and germicide.

Physical properties about 4-Chloro-3,5-xylenol are: (1)ACD/LogP: 3.35; (2)ACD/LogD (pH 5.5): 3.35; (3)ACD/LogD (pH 7.4): 3.34; (4)ACD/BCF (pH 5.5): 205.53; (5)ACD/BCF (pH 7.4): 204.65; (6)ACD/KOC (pH 5.5): 1574.57; (7)ACD/KOC (pH 7.4): 1567.83; (8)#H bond acceptors: 1; (9)#H bond donors: 1; (10)#Freely Rotating Bonds: 1; (11)Polar Surface Area: 20.23 Å2; (12)Index of Refraction: 1.558; (13)Molar Refractivity: 42.67 cm3; (14)Molar Volume: 132.3 cm3; (15)Polarizability: 16.91×10-24cm3; (16)Surface Tension: 40.2 dyne/cm; (17)Density: 1.183 g/cm3; (18)Flash Point: 105.9 °C; (19)Enthalpy of Vaporization: 50.27 kJ/mol; (20)Boiling Point: 246 °C at 760 mmHg; (21)Vapour Pressure: 0.0177 mmHg at 25°C.

Preparation: this chemical can be prepared by 3,5 - dichloro-dimethyl phenol and acid, also can be prepared by 3,5 - dimethyl phenol and chlorine catalyzed by zinc.

Uses of 4-Chloro-3,5-xylenol: it can be used to produce 2,6-bis-bromomethyl-4-chloro-3,5-dimethyl-phenol. It will need reagent HBr(g) and solvent acetic acid with reaction time of 30 min. The yield is about 57%.

When you are using this chemical, please be cautious about it as the following:
It is harmful if swallowed and may cause sensitisation by skin contact. Besides, this chemical is irritating to eyes and skin. When you are using it, wear suitable gloves and avoid contact with skin.

You can still convert the following datas into molecular structure:
(1)Canonical SMILES: CC1=CC(=CC(=C1Cl)C)O
(2)InChI: InChI=1S/C8H9ClO/c1-5-3-7(10)4-6(2)8(5)9/h3-4,10H,1-2H3
(3)InChIKey: OSDLLIBGSJNGJE-UHFFFAOYSA-N

The toxicity data is as follows:

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
mouse LD50 intraperitoneal 115gm/kg (115000mg/kg)   Journal of the American Pharmaceutical Association, Scientific Edition. Vol. 41, Pg. 595, 1952.
mouse LD50 oral 1gm/kg (1000mg/kg) BEHAVIORAL: ALTERED SLEEP TIME (INCLUDING CHANGE IN RIGHTING REFLEX)

BEHAVIORAL: ATAXIA

GASTROINTESTINAL: OTHER CHANGES
Science Reports of the Research Institutes, Tohoku University, Series C: Medicine. Vol. 36(1-4), Pg. 10, 1989.
rat LD50 oral 3830mg/kg (3830mg/kg) LUNGS, THORAX, OR RESPIRATION: OTHER CHANGES

GASTROINTESTINAL: OTHER CHANGES

KIDNEY, URETER, AND BLADDER: OTHER CHANGES
Journal of the American College of Toxicology. Vol. 4(5), Pg. 147, 1985.
women LDLo oral 6mL/kg (6mL/kg) VASCULAR: BP LOWERING NOT CHARACTERIZED IN AUTONOMIC SECTION

LUNGS, THORAX, OR RESPIRATION: RESPIRATORY STIMULATION

KIDNEY, URETER, AND BLADDER: URINE VOLUME DECREASED
Postgraduate Medical Journal. Vol. 53, Pg. 229, 1977.

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