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4-PHENYLPHENOL | ||
PRODUCT IDENTIFICATION |
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CAS NO. | 92-69-3 |
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EINECS NO. | 202-179-2 | |
FORMULA | C6H5C6H4OH | |
MOL WT. | 170.21 | |
H.S. CODE |
2907.19.8000 | |
TOXICITY |
Oral rat LD50; 2000 mg/kg | |
SYNONYMS | p-Phenylphenol; 1,1'-Biphenyl-4-ol; (1,1-Biphenyl)-4-ol; | |
4-Hydroxdiphenyl; 4-Hydroxybiphenyl; Biphenylol; Biphenyl-4-ol; p-Xenol; Orthoxenol; 4-Biphenylol; p-Xonal; p-Hydroxydipbenyl; Paraxenol; 4-Diphenylol; 4-Phenylphenol; Phenol p-phenyl; Paraxenol; para-Hydroxydiphenyl; para-Phenylphenol; Other RN: 61840-56-0, 110617-59-9 | ||
SMILES | c1(c2ccccc2)ccc(O)cc1 | |
CLASSIFICATION |
Phenol, Biphenyl |
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EXTRA NOTES |
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PHYSICAL AND CHEMICAL PROPERTIES |
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PHYSICAL STATE | white flakes, mild odor | |
MELTING POINT | 165 - 167 C | |
BOILING POINT |
307 C | |
SPECIFIC GRAVITY |
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SOLUBILITY IN WATER | 0.7 g/l at 20 C | |
SOLVENT SOLUBILITY |
soluble in alkalies, in most organic solvents | |
VAPOR DENSITY |
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pKa | 9.55 (Dissociation Constant at 25 C) | |
log P | 3.2 (Octanol-water) | |
VAPOR PRESSURE | 1.86E-05 (mmHg at 25 C) | |
HENRY LAW CONSTANT | 5.23E-08 (atm-m3/mole at 25 C) | |
OH RATE CONSTANT | 2.73E-11 (cm3/molecule-sec at 25 C Atmospheric) | |
REFRACTIVE INDEX |
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AUTOIGNITION |
250 C | |
NFPA RATINGS | Health: 2; Flammability: 1; Reactivity: 0 | |
FLASH POINT |
165 C | |
STABILITY |
Stable under ordinary conditions | |
EXTERNAL LINKS & GENERAL DESCRIPTION |
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PubChem Compound Summary - 4-Phenylphenol Local: |
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SALES SPECIFICATION | ||
APPEARANCE |
white flakes | |
ASSAY |
98.0% min |
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MELTING POINT | 165 - 167 C | |
MOISTURE |
0.1% max |
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TRANSPORTATION | ||
PACKING |
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HAZARD CLASS | ||
UN NO. |
Not regulated | |
SAFETY INFORMATION | ||
HAZARD OVERVIEW |
Causes skin irritation. Toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment. May cause eye and respiratory tract irritation. Target Organs: Skin. |
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GHS |
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SIGNAL WORD | Warning | |
PICTOGRAMS |
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HAZARD STATEMENTS |
H315: Causes skin irritation |
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PRECAUTIONARY STATEMENTS |
P273: Avoid release to the environment |
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EC DIRECTIVES |
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HAZARD CODES |
Xi Irritant |
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RISK PHRASES |
36/37/38: Irritating to eyes, respiratory system and skin. |
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SAFETY PHRASES |
37: Wear suitable gloves. |
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GENERAL DESCRIPTION OF BIPHENYL | ||
Biphenyl (also called Diphenyl, but exactly one of two compounds. The other is o-phenylphenol, used to prevent the growth of moulds ) is an aromatic hydrocarbon; molecule structure is composed of two six-sided carbon rings connected at one carbon site on each ring. Pure biphenyl is a toxic colourless crystalline solid with a pleasant odour; melting point 70 C, boiling point 255 C, which gives plates or monoclinic prismatic crystals; it is insoluble in water but soluble in ordinary organic solvents. It is directly used in the preservation of citrus fruits as a fungistat in transportation containers. It is a raw material for polychlorinated diphenyls (PCB) in which chlorine replaces hydrogen in biphenyls. There are 209 chlorinated isomers of biphenyl theoretically. But PCBs are referred to the biphenyl compounds with one to ten chlorine substitutions. PCBs are used heat-transfer agents and as electric insulators that block the flow of electric current across in electrical equipments. They are known as environmental pollution materials which are accumulated in animal tissues and cause toxic effects including carcinogenesis. Biphenyl is used as an intermediate for the production of a wide range of organic compounds (e.g. emulsifiers, optical brighteners, crop protection products, plastics), as a heat transfer medium alone or with diphenyl ether in heating fluids, as a dyestuff carrier for textiles and copying paper and as a solvent in pharmaceutical production. Aminodiphenyls are used as rubber antioxidants and intermediates for the synthesis of organic compounds ( azo dyes and pharmaceuticals). Biphenyl derivatives are used as an intermediate for the synthesis of organic compounds including pharmaceuticals, antifungal agents, optical brightening agents and dyes. Biphenyl compounds also used in luminescence chemistry, spectrophotometric analysis, molecular chemistry, and as a stating material for organometallic-complexes. | ||
PRICE INFORMATION | ||
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