morin
2',3,4',5,7-pentahydroxyflavone
 
Notes:
Constit. of various woods, e.g. Morus alba (white mulberry). First isol. in 1830
  • BOC Sciences
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      Product(s):
      480-16-0 Morin >98%
      Morin induces caspase-dependent apoptosis through extrinsic pathway by upregulating Fas receptor as well as through the intrinsic pathway by modulating Bcl- anti-cancer
       
       
  • Charkit Chemical
    • Charkit Chemical Corporation
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      about: Since 1982, Charkit has been committed to expanding the markets we serve as our roster of products and services continues to grow with us. Our substantial portfolio of personal care ingredients now include a wide array of luxury and exotic components to compliment the key products we have always offered. We have expanded our offerings to the nutraceutical, industrial, and resin markets with a growing roster of versatile and unique ingredients. We continue to lead the way in our traditional markets such as Metal and Water Treatment, Imaging, Flavor & Fragrance, Aroma and Food. Our Pharmaceutical offerings continue to expand, still anchored by the Boronic Derivatives that meet the demands of Suzuki coupling reactions. Please contact us to learn how we can help you reach your goals.
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      Product(s):
      MORIN, NEW PROCESS
       
Synonyms   Articles   Notes   Search
CAS Number: 480-16-0Picture of molecule3D/inchi
Other(deleted CASRN): 11128-85-1
ECHA EINECS - REACH Pre-Reg: 207-542-9
FDA UNII: 8NFQ3F76WR
Nikkaji Web: J1.542C
Beilstein Number: 0327474
MDL: MFCD00217054
XlogP3: 1.50 (est)
Molecular Weight: 302.23910000
Formula: C15 H10 O7
BioActivity Summary: listing
NMR Predictor: Predict (works with chrome 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
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Physical Properties:
Assay: 95.00 to 100.00 % 
Food Chemicals Codex Listed: No
Boiling Point: 645.50 °C. @ 760.00 mm Hg (est)
Flash Point: 481.00 °F. TCC ( 249.30 °C. ) (est)
logP (o/w): 1.610 (est)
Soluble in:
 water, 250 mg/L @ 20 °C (exp)
 water, 2192 mg/L @ 25 °C (est)
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Organoleptic Properties:
 
Odor and/or flavor descriptions from others (if found).
 
 
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Cosmetic Information:
None found
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Suppliers:
Abbey Color
Natural Yellow 11
Alfa Biotechnology
For experimental / research use only.
Morin 98%
BOC Sciences
For experimental / research use only.
Morin >98%
Odor: characteristic
Use: Morin induces caspase-dependent apoptosis through extrinsic pathway by upregulating Fas receptor as well as through the intrinsic pathway by modulating Bcl- anti-cancer
Charkit Chemical
MORIN, NEW PROCESS
ExtraSynthese
For experimental / research use only.
Morin (HPLC) ≥99%
Sigma-Aldrich: Sigma
For experimental / research use only.
Morin hydrate powder
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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:
intraperitoneal-mouse LD50  555 mg/kg
BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY) LUNGS, THORAX, OR RESPIRATION: RESPIRATORY DEPRESSION BEHAVIORAL: MUSCLE WEAKNESS
Archives Internationales de Pharmacodynamie et de Therapie. Vol. 123, Pg. 395, 1960.

Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
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Safety in Use Information:
Category: natural substances and extractives
Recommendation for morin usage levels up to:
 not for fragrance use.
 
Recommendation for morin flavor usage levels up to:
 not for flavor use.
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Safety References:
EPI System: View
Chemical Carcinogenesis Research Information System: Search
Cancer Citations: Search
Toxicology Citations: Search
EPA Substance Registry Services (TSCA): 480-16-0
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 5281670
National Institute of Allergy and Infectious Diseases: Data
WGK Germany: 3
 2-(2,4-dihydroxyphenyl)-3,5,7-trihydroxychromen-4-one
Chemidplus: 0000480160
RTECS: LK8749000 for cas# 480-16-0
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References:
 2-(2,4-dihydroxyphenyl)-3,5,7-trihydroxychromen-4-one
NIST Chemistry WebBook: Search Inchi
Canada Domestic Sub. List: 480-16-0
Pubchem (cid): 5281670
Pubchem (sid): 135017718
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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
Golm Metabolome Database: Search
KEGG (GenomeNet): C10105
HMDB (The Human Metabolome Database): HMDB30796
FooDB: FDB002736
Export Tariff Code: 3203.00.5000
VCF-Online: VCF Volatile Compounds in Food
ChemSpider: View
Wikipedia: View
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Potential Blenders and core components note
 
None Found
 
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Potential Uses:
None Found
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Occurrence (nature, food, other): note
 mulberry wood
Search Trop  Picture
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Synonyms:
 calico yellow
2-(2,4-dihydroxyphenyl)-3,5,7-trihydroxychromen-4-one
 morin hydrate
 natural yellow 11
2',3,4',5,7-pentahydroxyflavone
 toxylon pomiferum
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