Product Name

  • Name

    2,5-Dimethylphenol

  • EINECS 202-461-5
  • CAS No. 95-87-4
  • Article Data136
  • CAS DataBase
  • Density 1.041 g/cm3
  • Solubility 1 g/100 mL (60 °C) in water
  • Melting Point 75-77 °C
  • Formula C8H10O
  • Boiling Point 211.1 °C at 760 mmHg
  • Molecular Weight 122.167
  • Flash Point 86.7 °C
  • Transport Information UN 2261 6.1/PG 2
  • Appearance White to cream colored crystals
  • Safety 26-36/37/39-45-61
  • Risk Codes 24/25-34-51/53
  • Molecular Structure Molecular Structure of 95-87-4 (2,5-Dimethylphenol)
  • Hazard Symbols ToxicT, DangerousN
  • Synonyms 2,5-Xylenol(8CI);1,2,5-Xylenol;1-Hydroxy-2,5-dimethylbenzene;2,5-Dimethylphenol;2-Hydroxy-p-xylene;3,6-Dimethylphenol;NSC 2599;p-Xylenol;
  • PSA 20.23000
  • LogP 2.00900

2,5-Dimethylphenol Consensus Reports

Reported in EPA TSCA Inventory.

2,5-Dimethylphenol Specification

The 2,5-Xylenol , with the register number 95-87-4, has other names as xylenol(2,5-) ; 1,2,5-xylenol ; 1,4-dimethyl-2-hydroxybenzene ; 1-hydroxy-2,5-dimethylbenzene ; 2,5-dimethyl-pheno ; 3,6-dimethylphenol ; 3,6-xylenol ; 6-methyl-m-cresol .

The characteristics of this kind of chemical are as the following:(1)#H bond acceptors:  1  ; (2)#H bond donors:  1  ; (3)#Freely Rotating Bonds:  1  ; (4)Polar Surface Area:  20.23 ; (5)Index of Refraction:  1.54  ; (6)Molar Refractivity:  37.78 cm ; (7)Molar Volume:  120.4 cm3  ; (8)Polarizability:  14.97 ×10-24 cm3  ; (9)Surface Tension:  37.2 dyne/cm  ; (10)Density:  1.014 g/cm ; (11)Flash Point:  86.7 °C  ; (12)Enthalpy of Vaporization:  46.57 kJ/mol  ; (13)Boiling Point:  211.1 °C at 760 mmHg  ; (14)Vapour Pressure:  0.128 mmHg at 25°C .

It is a kind of white acicular crystalline and it is soluble in water and ethanol. Besides, it could sublimate and could volatile with steam. As for its product categories, they are various, including aromatic phenols;intermediatesofgemfibroil.

As being a kind of toxic chemical, it could cause damage to health and if in contact with skin and if swallowed, it will bring great damage to our health. For another thing, it is dangerous for the environment for it is toxic to aquatic organisms, which may cause long-term adverse effects in the aquatic environment; And it could also present an immediate or delayed danger to one or more components of the environment. Except all these, it will cause burns.

Because of the harmful properties, you should be very careful while dealing with this chemical. Wear suitable protective clothing, gloves and eye/face protection; If in case of contacting with eyes, rinse immediately with plenty of water and seek medical advice; If in case of accident or if you feel unwell seek medical advice immediately (show the label where possible). Beside, remember to avoid releasing to the environment and refer to special instructions/safety data sheet. If you need more safety information, you could refer to the WGK Germany  3.
 
When it comes to its usage, it is widely applied in many fields, such as being the intermediate in organic synthesis and be used in dying and the synthesis of lipid-lowering drugs of Gemfibrozil. What's more, there is a simple way to get this chemical. Prepare the raw material of xylidine and then have the diazotization and the hydrolyzation. Then you could get it.

Below are the toxicity of this chemical:

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
mouse LD50 oral 383mg/kg (383mg/kg) BEHAVIORAL: ATAXIA

BEHAVIORAL: MUSCLE CONTRACTION OR SPASTICITY)

LUNGS, THORAX, OR RESPIRATION: DYSPNEA
Hygiene and Sanitation Vol. 33(7-9), Pg. 329, 1968.
rabbit LD50 oral 938mg/kg (938mg/kg) BEHAVIORAL: ATAXIA

LUNGS, THORAX, OR RESPIRATION: DYSPNEA

BEHAVIORAL: MUSCLE CONTRACTION OR SPASTICITY)
Hygiene and Sanitation Vol. 33(7-9), Pg. 329, 1968.
rat LD50 oral 444mg/kg (444mg/kg)   Gigiena Truda i Professional'naya Patologiya v Estonskoi SSR. Labor Hygiene and Occupational Pathology in the Estonian SSR. Vol. 8, Pg. 145, 1972.
rat LD50 unreported 730mg/kg (730mg/kg) BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD Journal of Pharmacology and Experimental Therapeutics. Vol. 53, Pg. 227, 1935.

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