jaceidin, 10173-01-0

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CODE148651 CODE148651
Product(s):
10173-01-0 Jaceidin

Name:	5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3,6-dimethoxychromen-4-one
CAS Number:	10173-01-0	3D/inchi
FDA UNII:	Search
Nikkaji Web:	J15.593D
XlogP3-AA:	2.80 (est)
Molecular Weight:	360.31912000
Formula:	C18 H16 O8
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:	647.80 °C. @ 760.00 mm Hg (est)
Flash Point:	461.00 °F. TCC ( 238.30 °C. ) (est)
logP (o/w):	1.560 (est)
Soluble in:
	water, 160.4 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.

Jaceidin

Coompo

For experimental / research use only.

Jaceidin from Plants ≥96%

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:
Not determined
Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined

Safety in Use Information:

Category:
natural substances and extractives
Recommendation for jaceidin usage levels up to:
	not for fragrance use.

Recommendation for jaceidin 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 :5464461

National Institute of Allergy and Infectious Diseases:Data

5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3,6-dimethoxychromen-4-one

Chemidplus:0010173010

References:

	5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3,6-dimethoxychromen-4-one
NIST Chemistry WebBook:	Search Inchi
Pubchem (cid):	5464461
Pubchem (sid):	135030535

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):	HMDB33819
FooDB:	FDB011984
VCF-Online:	VCF Volatile Compounds in Food
ChemSpider:	View
Wikipedia:	View

Potential Blenders and core components note

None Found

Potential Uses:

None Found

Occurrence (nature, food, other):note

	achillea biebersteinu Search Trop Picture
	chamomile sweet false chamomile plant Search Trop Picture
	cherry sweet cherry Search Trop Picture
	varthemia iphionoides Search Trop Picture

Synonyms:

4H-1-	benzopyran-4-one, 5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3,6-dimethoxy-
5,7-	dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3,6-dimethoxy-4H-1-benzopyran-4-one
5,7-	dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3,6-dimethoxy-4H-chromen-4-one
5,7-	dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3,6-dimethoxychromen-4-one
	jaceidine
	quercetagetin 3,3',6-trimethyl ether

Articles:

PubMed:Short photoirradiation induces flavonoid synthesis and increases its production in postharvest vegetables.

PubMed:Protective effect on human lymphocytes of some flavonoids isolated from two Achillea species.

PubMed:One new triterpene ester from Nepeta suavis.

PubMed:Antiplatelet activity of Varthemia iphionoides.

PubMed:Bioactive flavonoids of Tanacetum parthenium revisited.

PubMed:The synthesis of jaceidin.

Notes:

Found in buds of Prunus avium (wild cherry)

jaceidin quercetagetin 3,3',6-trimethyl ether

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Articles:

jaceidin
quercetagetin 3,3',6-trimethyl ether