2-(hydroxymethyl) anthraquinone
9,10-anthracenedione, 2-(hydroxymethyl)-
Identification
| Name | 2-(hydroxymethyl) anthraquinone |
| IUPAC | 2-(hydroxymethyl)anthracene-9,10-dione |
| CAS Number | 17241-59-7 |
| EINECS | 241-274-3 |
| FDA UNII | Search |
| Molecular Formula | C15 H10 O3 |
| Molecular Weight | 238.24230000 |
| MDL Number | MFCD00001236 |
| Nikkaji Number | J208.594A |
| Beilstein | 2120452 |
| XlogP3 | 2.70 (est) |
Regulatory
Physical Properties
| Assay | 95.00 to 100.00 |
| Food Chemicals Codex Listed | No |
| Boiling Point | 472.90 °C. @ 760.00 mm Hg (est) |
| Flash Point | 489.00 °F. TCC ( 253.90 °C. ) (est) |
| logP (o/w) | 2.200 (est) |
| Soluble in | water, 58.35 mg/L @ 25 °C (est) |
No sensory data available
Safety Information
| Preferred SDS | View |
| Oral/Parenteral Toxicity | Not determined |
| Dermal Toxicity | Not determined |
| Inhalation Toxicity | Not determined |
GHS Classification
['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']
Safety in Use
| Category | natural substances and extractives |
| Recommendation for 2-(hydroxymethyl) anthraquinone usage levels up to | not for fragrance use. |
| Recommendation for 2-(hydroxymethyl) anthraquinone flavor usage levels up to | not for flavor use. |
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Potential Uses
Natural Occurrence
Synonyms
9,10-
anthracenedione, 2-(hydroxymethyl)-
anthraquinone, 2-(hydroxymethyl)-
2-(
hydroxymethyl)anthracene-9,10-dione
2-(
hydroxymethyl)anthraquinone
2-
hydroxymethylanthraquinone
PubMed:
Photoremovable protecting groups as controlled-release device for sex pheromone.
PubMed:
Long-range intramolecular photoredox reaction via coupled charge and proton transfer of triplet excited anthraquinones mediated by water.
PubMed:
Formal intramolecular photoredox chemistry of anthraquinones in aqueous solution: photodeprotection for alcohols, aldehydes and ketones.
PubMed:
A simple and smart oxygen sensor based on the intrazeolite reactions of a substituted anthraquinone.
PubMed:
[Studies on the chemical constituents from stem of Chirita longgangensis var. Hongyao].
PubMed:
Antibacterial activity of Tabebuia impetiginosa Martius ex DC (Taheebo) against Helicobacter pylori.
PubMed:
Excited state intramolecular redox reaction of 2-(hydroxymethyl)anthraquinone in aqueous solution.
PubMed:
Effect of a cytotoxic analog of LH-RH (T-98) on the growth of estrogen-dependent MXT mouse mammary cancers: correlations between growth characteristics and EGF receptor content of tumors.
PubMed:
LH-RH analogue carrying a cytotoxic radical is internalized by rat pituitary cells in vitro.
PubMed:
Effect of luteinizing hormone-releasing hormone analogs containing cytotoxic radicals on the function of rat pituitary cells: tests in a long term superfusion system.
PubMed:
Evaluation of binding of cytotoxic analogs of luteinizing hormone-releasing hormone to human breast cancer and mouse MXT mammary tumor.
PubMed:
Inhibition of growth of experimental prostate cancer in rats by LH-RH analogs linked to cytotoxic radicals.
PubMed:
Short-chain analogs of luteinizing hormone-releasing hormone containing cytotoxic moieties.
PubMed:
Effect of luteinizing hormone-releasing hormone analogs containing cytotoxic radicals on growth of estrogen-independent MXT mouse mammary carcinoma in vivo.
PubMed:
Analogues of luteinizing hormone-releasing hormone containing cytotoxic groups.
PubMed:
2-Methylanthraquinone derivatives as potential bioreductive alkylating agents.
PubMed:
Studies in the biochemistry of micro-organisms: Emodic acid (4:5:7-trihydroxyanthraquinone-2-carboxylic acid) and omega-hydroxyemodin (4:5:7-trihydroxy-2-(hydroxymethyl)-anthraquinone), metabolic products of a strain of Penicillium cyclopium Westling.