2-(hydroxymethyl) anthraquinone

9,10-anthracenedione, 2-(hydroxymethyl)-

CAS: 17241-59-7 C15 H10 O3 MW: 238.24230000

Identification

Name2-(hydroxymethyl) anthraquinone
IUPAC2-(hydroxymethyl)anthracene-9,10-dione
CAS Number17241-59-7
EINECS241-274-3
FDA UNIISearch
Molecular FormulaC15 H10 O3
Molecular Weight238.24230000
MDL NumberMFCD00001236
Nikkaji NumberJ208.594A
Beilstein2120452
XlogP32.70 (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 SDSView
Oral/Parenteral ToxicityNot determined
Dermal ToxicityNot determined
Inhalation ToxicityNot determined

GHS Classification

['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']

Safety in Use

Categorynatural substances and extractives
Recommendation for 2-(hydroxymethyl) anthraquinone usage levels up tonot for fragrance use.
Recommendation for 2-(hydroxymethyl) anthraquinone flavor usage levels up tonot for flavor use.

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Potential Uses

None Found

Natural Occurrence

turmeric rhizome turmeric wild turmeric leaf

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.