3',4',7-trihydroxyflavone, 2150-11-0

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CODE148575 CODE148575
Product(s):
2150-11-0 3',4',7-Trihydroxyflavone >9%
3'4'7-Trihydroxyflavone is a natural flavonoid found in the seeds of Cassia occidentalis. 3',4',7-Trihydroxyflavone can prevent apoptotic cell death in neuronal cells from hydrogen peroxide-induced oxidative stress.

CAS Number:	2150-11-0	3D/inchi
FDA UNII:	Search
Nikkaji Web:	J548.247J
Beilstein Number:	0253031
MDL:	MFCD00017434
XlogP3:	2.90 (est)
Molecular Weight:	270.24070000
Formula:	C15 H10 O5
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:	572.80 °C. @ 760.00 mm Hg (est)
Flash Point:	435.00 °F. TCC ( 224.00 °C. ) (est)
logP (o/w):	2.840 (est)
Soluble in:
	water, 1188 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.

3',4',7-Trihydroxyflavone >9%

Odor: characteristic

Use: 3'4'7-Trihydroxyflavone is a natural flavonoid found in the seeds of Cassia occidentalis. 3',4',7-Trihydroxyflavone can prevent apoptotic cell death in neuronal cells from hydrogen peroxide-induced oxidative stress.

ExtraSynthese

For experimental / research use only.

3',4',7-Trihydroxyflavone (HPLC) ≥90%

Safety Information:


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:
intraperitoneal-mouse LD > 1000 mg/kg Farmaco, Edizione Scientifica. Vol. 38, Pg. 67, 1983.
Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined

Safety in Use Information:

Category:
natural substances and extractives
Recommendation for 3',4',7-trihydroxyflavone usage levels up to:
	not for fragrance use.

Recommendation for 3',4',7-trihydroxyflavone 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 :5322065

National Institute of Allergy and Infectious Diseases:Data

2-(3,4-dihydroxyphenyl)-7-hydroxychromen-4-one

Chemidplus:0002150110

References:

	2-(3,4-dihydroxyphenyl)-7-hydroxychromen-4-one
NIST Chemistry WebBook:	Search Inchi
Pubchem (cid):	5322065
Pubchem (sid):	135121602

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):	HMDB34004
FooDB:	FDB012021
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

	alfalfa Search Trop Picture
	bean fava bean Search Trop Picture
	fenugreek Search Trop Picture

Synonyms:

4H-1-	benzopyran-4-one, 2-(3,4-dihydroxyphenyl)-7-hydroxy-
2-(3,4-	dihydroxyphenyl)-7-hydroxy-4H-1-benzopyran-4-one
2-(3,4-	dihydroxyphenyl)-7-hydroxychromen-4-one
7,3',4'-	trihydroxyflavone

Articles:

PubMed:New flavan and alkyl alpha,beta-lactones from the stem bark of Horsfieldia superba.

PubMed:3,3',4',5,5'-Pentahydroxyflavone is a potent inhibitor of amyloid β fibril formation.

PubMed:Flavonoids from Sudanese Albizia zygia (Leguminosae, subfamily Mimosoideae), a plant with antimalarial potency.

PubMed:A new 5-deoxyflavone glycoside from the aerial parts of Calea clausseniana.

PubMed:Bioactive constituents of Spatholobus suberectus in regulating tyrosinase-related proteins and mRNA in HEMn cells.

PubMed:Geranylated phenolic constituents from the fruits of Artocarpus nobilis.

PubMed:Antioxidant activity from the stem bark of Albizzia julibrissin.

PubMed:IDENTIFICATION OF 3',4',7-TRIHYDROXYFLAVONE IN LADINO CLOVER.

Notes:

None found

3',4',7-trihydroxyflavone 4H-1-benzopyran-4-one, 2-(3,4-dihydroxyphenyl)-7-hydroxy-

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Articles:

3',4',7-trihydroxyflavone
4H-1-benzopyran-4-one, 2-(3,4-dihydroxyphenyl)-7-hydroxy-