Difference between pages "Volatile organic compound" and "4-chloro-3-methylphenol"
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== Description == | == Description == | ||
− | + | White crystals with a phenolic odor that have been used as a topical antiseptic. Chlorocresol dissolved in [[ethyl%20alcohol|ethanol]] has been used as a [[fungicide|fungicide]] on [[paint|paintings]], [[parchment|parchment]], and [[stone|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. | ||
+ | |||
+ | {| class="wikitable" | ||
+ | |- | ||
+ | ! scope="row"| Composition | ||
+ | | C7H7ClO | ||
+ | |- | ||
+ | ! scope="row"| CAS | ||
+ | | 59-50-7 | ||
+ | |- | ||
+ | ! scope="row"| Melting Point | ||
+ | | 55.5 - 66 C | ||
+ | |- | ||
+ | ! scope="row"| Molecular Weight | ||
+ | | mol. wt. = 142.58 | ||
+ | |- | ||
+ | ! scope="row"| 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: [http://www.fishersci.ca/msds2.nsf/0/3E4243A8EDA2220F85256CA50000AAF8/$file/MSDS-97739.html?open MSDS] |
+ | |||
+ | == Comparisons == | ||
− | + | [[media:download_file_14.pdf|pdf]] | |
==Resources and Citations== | ==Resources and Citations== | ||
− | * P. | + | * ''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 | ||
+ | |||
[[Category:Materials database]] | [[Category:Materials database]] |
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