EU/US Properties Organoleptics Cosmetics Suppliers Safety Safety in use Safety references References Other Blenders Uses Occurrence Synonyms Articles Notes
 

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

Supplier Sponsors

Name:2-(hydroxymethyl)anthracene-9,10-dione
CAS Number: 17241-59-7Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg:241-274-3
FDA UNII: Search
Nikkaji Web:J208.594A
Beilstein Number:2120452
MDL:MFCD00001236
XlogP3:2.70 (est)
Molecular Weight:238.24230000
Formula:C15 H10 O3
BioActivity Summary:listing
NMR Predictor:Predict (works with chrome, Edge or firefox)
Category:natural substances and extractives
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar:Search
Google Books:Search
Google Scholar: with word "volatile"Search
Google Scholar: with word "flavor"Search
Google Scholar: with word "odor"Search
Google Patents:Search
US Patents:Search
EU Patents:Search
Pubchem Patents:Search
PubMed:Search
NCBI:Search
 
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)
 
Organoleptic Properties:
Odor and/or flavor descriptions from others (if found).
 
Cosmetic Information:
None found
 
Suppliers:
BOC Sciences
For experimental / research use only.
2-(Hydroxymethyl)anthraquinone >95%
Odor: characteristic
Use: 2-(Hydroxymethyl)anthraquinone is found in the dried inner bark (taheebo) of Tabebuia impetiginosa.
Santa Cruz Biotechnology
For experimental / research use only.
2-(Hydroxymethyl)anthraquinone ≥96%
Sigma-Aldrich: Aldrich
For experimental / research use only.
2-(Hydroxymethyl)anthraquinone 97%
 
Safety Information:
Preferred SDS: View
 
Hazards identification
 
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
 
Pictogram
 
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
Not determined
Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
 
Safety in Use Information:
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.
 
Safety References:
EPI System: View
Chemical Carcinogenesis Research Information System:Search
AIDS Citations:Search
Cancer Citations:Search
Toxicology Citations:Search
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :87014
National Institute of Allergy and Infectious Diseases:Data
WGK Germany:3
2-(hydroxymethyl)anthracene-9,10-dione
Chemidplus:0017241597
RTECS:CB7600000 for cas# 17241-59-7
 
References:
 2-(hydroxymethyl)anthracene-9,10-dione
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):87014
Pubchem (sid):135043640
 
Other Information:
(IUPAC):Atomic Weights of the Elements 2011 (pdf)
Videos:The Periodic Table of Videos
tgsc:Atomic Weights use for this web site
(IUPAC):Periodic Table of the Elements
CHEBI:View
CHEMBL:View
KEGG (GenomeNet):C10354
HMDB (The Human Metabolome Database):Search
FooDB:FDB005316
Export Tariff Code:2914.61.0000
VCF-Online:VCF Volatile Compounds in Food
ChemSpider:View
 
Potential Blenders and core components note
None Found
 
Potential Uses:
None Found
 
Occurrence (nature, food, other):note
 turmeric rhizome
Search Trop Picture
 turmeric wild turmeric leaf
Search Trop Picture
 
Synonyms:
9,10-anthracenedione, 2-(hydroxymethyl)-
 anthraquinone, 2-(hydroxymethyl)-
2-(hydroxymethyl)anthracene-9,10-dione
2-(hydroxymethyl)anthraquinone
2-hydroxymethylanthraquinone
 

Articles:

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.
 
Notes:
None found
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