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Category: antioxidants
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Physical Properties:
| Assay: | 95.00 to 100.00 %
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| Food Chemicals Codex Listed: | No |
| Melting Point: | 76.00 °C. @ 760.00 mm Hg
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| Boiling Point: | 225.10 °C. @ 760.00 mm Hg (est)
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| Vapor Pressure: | 0.014000 mmHg (est) |
| Flash Point: | 194.00 °F. TCC ( 89.90 °C. ) (est)
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| logP (o/w): | 1.710 |
| Soluble in: |
| | water, 2596 mg/L @ 25 °C (est) |
Organoleptic Properties:
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| Odor and/or flavor descriptions from others (if found). |
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Cosmetic Information:
Suppliers:
Safety Information:
| Preferred SDS: View |
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| Hazards identification |
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| Classification of the substance or mixture |
| GHS Classification in accordance with 29 CFR 1910 (OSHA HCS) |
| None found. |
| GHS Label elements, including precautionary statements |
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| Pictogram | |
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| Hazard statement(s) |
| None found. |
| Precautionary statement(s) |
| None found. |
| Oral/Parenteral Toxicity: |
oral-guinea pig LD50 1775 mg/kg BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY)
LUNGS, THORAX, OR RESPIRATION: DYSPNEA
BEHAVIORAL: ATAXIA Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 51(2), Pg. 72, 1986.
intraperitoneal-mouse LD50 300 mg/kg National Technical Information Service. Vol. AD277-689
oral-mouse LD50 2625 mg/kg LUNGS, THORAX, OR RESPIRATION: DYSPNEA
BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY)
BEHAVIORAL: ATAXIA Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 51(2), Pg. 72, 1986.
oral-rat LD50 2635 mg/kg BEHAVIORAL: ATAXIA
BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY)
LUNGS, THORAX, OR RESPIRATION: DYSPNEA Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 51(2), Pg. 72, 1986.
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| Dermal Toxicity: |
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Not determined
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| Inhalation Toxicity: |
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Not determined
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Safety in Use Information:
| Category: | antioxidants |
| Recommendation for thioacetanilide usage levels up to: | | | not for fragrance use.
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| Recommendation for thioacetanilide flavor usage levels up to: |
| | not for flavor use.
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Safety References:
References:
Other Information:
Potential Blenders and core components note
Potential Uses:
Occurrence (nature, food, other): note
Synonyms:
| | ethanethioamide, N-phenyl- | | N- | phenyl thioacetamide | | 1-( | phenylamino)ethane-1-thione | | N- | phenylethanethioamide | | N- | phenylethanthioamid | | N- | phenylthioacetamide |
Articles:
| PubMed: | Arylazolylthioacetanilide. Part 11: design, synthesis and biological evaluation of 1,2,4-triazole thioacetanilide derivatives as novel non-nucleoside HIV-1 reverse transcriptase inhibitors. |
| PubMed: | Arylazolyl(azinyl)thioacetanilides. Part 10: design, synthesis and biological evaluation of novel substituted imidazopyridinylthioacetanilides as potent HIV-1 inhibitors. |
| PubMed: | Arylazolyl(azinyl)thioacetanilide. Part 9: Synthesis and biological investigation of thiazolylthioacetamides derivatives as a novel class of potential antiviral agents. |
| PubMed: | 1,2,3-thiadiazole thioacetanilides. Part 2: Synthesis and biological evaluation of a new series of 2-{[4-(3,4-dichlorophenyl)-1,2,3-thiadiazol-5-yl]sulfanyl}acetanilides as HIV-1 inhibitors. |
| PubMed: | 1,2,3-Selenadiazole thioacetanilides: synthesis and anti-HIV activity evaluation. |
| PubMed: | Synthesis and biological evaluation of imidazole thioacetanilides as novel non-nucleoside HIV-1 reverse transcriptase inhibitors. |
| PubMed: | Application of beta-(2-chloroaroyl)thioacetanilide in synthesis(III): an efficient three-component synthesis of thiochromeno[2,3-b]pyridines catalyzed by KF/neutral Al2O3 co-operated with PEG 6000 under microwave irradiation. |
| PubMed: | 1,2,3-Thiadiazole thioacetanilides as a novel class of potent HIV-1 non-nucleoside reverse transcriptase inhibitors. |
| PubMed: | Thioacetanilide at 120 K. |
| PubMed: | Application of beta-(2-chloroaroyl) thioacetanilides in synthesis: an unusual and highly efficient access to thiochromeno[2,3-b]pyridine derivatives. |
| PubMed: | Synthesis and biological evaluation of new 3-substituted indole derivatives as potential anti-inflammatory and analgesic agents. |
| PubMed: | Tetrazole thioacetanilides: potent non-nucleoside inhibitors of WT HIV reverse transcriptase and its K103N mutant. |
| PubMed: | Synthesis, anticonvulsant, and anti-inflammatory evaluation of some new benzotriazole and benzofuran-based heterocycles. |
| PubMed: | Correlation analyses for bimolecular nucleophilic substitution reactions of chloroacetanilide herbicides and their structural analogs with environmentally relevant nucleophiles. |
| PubMed: | Optical analysis of the cirrhotic liver by near-infrared time-resolved spectroscopy. |
| PubMed: | [Substantiation of maximum permissible levels of thioacylanilide in the air of work areas]. |
| PubMed: | The metabolism of thioacetanilide in the rat. |
| PubMed: | Determination of some organic thio-compounds by precipitation of mercuric sulphide from mercury(II) ammine complexes-I Determination of thioacetamide and thioacetanilide. |
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