Difference between revisions of "4-chloro-3-methylphenol"
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chlorocresol; p-chloro m-cresol; parachlorometacresol; 4-chloro-m-cresol; CMC; 2-chloro-5-hydroxytoluene | chlorocresol; p-chloro m-cresol; parachlorometacresol; 4-chloro-m-cresol; CMC; 2-chloro-5-hydroxytoluene | ||
| − | == | + | == Physical and Chemical Properties == |
Soluble in alcohol, benzene, chloroform, ether, acetone, mineral spirits, oils, terpenes, and aqueous alkaline solutions. | Soluble in alcohol, benzene, chloroform, ether, acetone, mineral spirits, oils, terpenes, and aqueous alkaline solutions. | ||
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! scope="row"| Melting Point | ! scope="row"| Melting Point | ||
| − | | 55.5 | + | | 55.5 - 66 C |
|- | |- | ||
! scope="row"| Molecular Weight | ! scope="row"| Molecular Weight | ||
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|- | |- | ||
! scope="row"| Boiling Point | ! scope="row"| Boiling Point | ||
| − | | 235 | + | | 235 C |
|} | |} | ||
| − | == | + | == Risks == |
| − | Toxic by ingestion. LD50 = 1830 mg/kg. Turns yellow with exposure to light and air. | + | * Toxic by ingestion. LD50 = 1830 mg/kg. Turns yellow with exposure to light and air. |
| − | Contact causes irritation, dermatitis and allergic reactions. | + | * Contact causes irritation, dermatitis and allergic reactions. |
| − | Fisher Scientific: [http://www.fishersci.ca/msds2.nsf/0/3E4243A8EDA2220F85256CA50000AAF8/$file/MSDS-97739.html?open MSDS] | + | * Fisher Scientific: [http://www.fishersci.ca/msds2.nsf/0/3E4243A8EDA2220F85256CA50000AAF8/$file/MSDS-97739.html?open MSDS] |
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== Comparisons == | == Comparisons == | ||
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[[media:download_file_14.pdf|pdf]] | [[media:download_file_14.pdf|pdf]] | ||
| − | + | ==Resources and Citations== | |
| − | |||
| − | == | ||
* ''The Merck Index'', Martha Windholz (ed.), Merck Research Labs, Rahway NJ, 10th edition, 1983 Comment: Entry # 2102 | * ''The Merck Index'', Martha Windholz (ed.), Merck Research Labs, Rahway NJ, 10th edition, 1983 Comment: Entry # 2102 | ||
Revision as of 14:53, 8 April 2022
Description
White crystals with a phenolic odor that have been used as a topical antiseptic. Chlorocresol dissolved in ethanol has been used as a Fungicide on paintings, Parchment, and Stone (Caneva et al 1991).
Synonyms and Related Terms
chlorocresol; p-chloro m-cresol; parachlorometacresol; 4-chloro-m-cresol; CMC; 2-chloro-5-hydroxytoluene
Physical and Chemical Properties
Soluble in alcohol, benzene, chloroform, ether, acetone, mineral spirits, oils, terpenes, and aqueous alkaline solutions.
| Composition | C7H7ClO |
|---|---|
| CAS | 59-50-7 |
| Melting Point | 55.5 - 66 C |
| Molecular Weight | mol. wt. = 142.58 |
| Boiling Point | 235 C |
Risks
- Toxic by ingestion. LD50 = 1830 mg/kg. Turns yellow with exposure to light and air.
- Contact causes irritation, dermatitis and allergic reactions.
- Fisher Scientific: MSDS
Comparisons
Resources and Citations
- The Merck Index, Martha Windholz (ed.), Merck Research Labs, Rahway NJ, 10th edition, 1983 Comment: Entry # 2102
- G.Caneva, M.P.Nugari, O.Salvadori, Biology in the Conservation of Works of Art, ICCROM, Rome, 1991
- Matte Paint: Its history and technology, analysis, properties and conservation treatment, Eric Hansen, Sue Walston, Mitchell Bishop (ed.), J. Paul Getty Trust, Los Angeles, Vol. 30 of AATA, 1993