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

2,4,6-trihydroxybenzaldehyde
benzaldehyde, 2,4,6-trihydroxy-

Supplier Sponsors

CAS Number: 487-70-7Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg:207-663-7
FDA UNII: I70C45KRO9
Nikkaji Web:J148.960G
Beilstein Number:2254429
MDL:MFCD00003329
XlogP3-AA:0.90 (est)
Molecular Weight:154.12162000
Formula:C7 H6 O4
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
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Google Scholar: with word "odor"Search
Google Patents:Search
US Patents:Search
EU Patents:Search
Pubchem Patents:Search
PubMed:Search
NCBI:Search
 
Physical Properties:
Food Chemicals Codex Listed: No
Boiling Point: 319.10 °C. @ 760.00 mm Hg (est)
Flash Point: 322.00 °F. TCC ( 161.00 °C. ) (est)
logP (o/w): 1.370 (est)
Soluble in:
 water, 7665 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.
2,4,6-trihydroxybenzaldehyde 95%
ExtraSynthese
For experimental / research use only.
Phloroglucinol carboxaldehyde
Santa Cruz Biotechnology
For experimental / research use only.
2,4,6-Trihydroxybenzaldehyde
Sigma-Aldrich: Aldrich
For experimental / research use only.
2,4,6-Trihydroxybenzaldehyde ≥97%
sds
TCI AMERICA
For experimental / research use only.
2,4,6-Trihydroxybenzaldehyde >98.0%(HPLC)
sds
 
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:
oral-mouse LD50 3200 mg/kg
Biochemical Journal. Vol. 34, Pg. 1196, 1940.

Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
 
Safety in Use Information:
Category:
natural substances and extractives
Recommendation for 2,4,6-trihydroxybenzaldehyde usage levels up to:
 not for fragrance use.
 
Recommendation for 2,4,6-trihydroxybenzaldehyde flavor usage levels up to:
 not for flavor use.
 
Safety References:
EPI System: View
AIDS Citations:Search
Cancer Citations:Search
Toxicology Citations:Search
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :68099
National Institute of Allergy and Infectious Diseases:Data
WGK Germany:2
2,4,6-trihydroxybenzaldehyde
Chemidplus:0000487707
RTECS:CU8440000 for cas# 487-70-7
 
References:
 2,4,6-trihydroxybenzaldehyde
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):68099
Pubchem (sid):135023808
 
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
CHEMBL:View
HMDB (The Human Metabolome Database):Search
Export Tariff Code:2912.49.2600
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
 found in nature
 
Synonyms:
 benzaldehyde, 2,4,6-trihydroxy-
 formylphloroglucinal
 phloroglucinaldehyde
 phloroglucinol carboxaldehyde
 

Articles:

PubMed:Proton and gallium(III) binding properties of a biologically active salicylidene acylhydrazide.
PubMed:Synthesis of nitrogen-doped activated graphene aerogel/gold nanoparticles and its application for electrochemical detection of hydroquinone and o-dihydroxybenzene.
PubMed:The identification of degradation products and degradation pathway of malvidin-3-glucoside and malvidin-3,5-diglucoside under microwave treatment.
PubMed:Modulation of Nrf2-dependent gene transcription by bilberry anthocyanins in vivo.
PubMed:The anthocyanin metabolites gallic acid, 3-O-methylgallic acid, and 2,4,6-trihydroxybenzaldehyde decrease human colon cancer cell viability by regulating pro-oncogenic signals.
PubMed:Contribution of gut bacteria to the metabolism of cyanidin 3-glucoside in human microbiota-associated rats.
PubMed:Synthesis, activity testing and molybdenum(VI) complexation of Schiff bases derived from 2,4,6-trihydroxybenzaldehyde investigated as xanthine oxidase inhibitors.
PubMed:An update of MALDI-TOF mass spectrometry in lipid research.
PubMed:Gut metabolites of anthocyanins, gallic acid, 3-O-methylgallic acid, and 2,4,6-trihydroxybenzaldehyde, inhibit cell proliferation of Caco-2 cells.
PubMed:UVA and UVB radiation-induced oxidation products of quercetin.
PubMed:First total synthesis of a polyunsaturated chromone metabolite isolated from the brown algae Zonaria tournefortii.
PubMed:Identification of Cabernet Sauvignon anthocyanin gut microflora metabolites.
PubMed:Antibacterial activities of phenolic benzaldehydes and benzoic acids against Campylobacter jejuni, Escherichia coli, Listeria monocytogenes, and Salmonella enterica.
PubMed:Intestinal bacterial metabolism of flavonoids and its relation to some biological activities.
 
Notes:
None found
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