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

kinetin
7H-purin-6-amine, N-(2-furanylmethyl)-

Supplier Sponsors

Name:N-(furan-2-ylmethyl)-7H-purin-6-amine
CAS Number: 525-79-1Picture of molecule3D/inchi
Other(deleted CASRN):33446-70-7
ECHA EINECS - REACH Pre-Reg:208-382-2
FDA UNII:P39Y9652YJ
Nikkaji Web:J6.656G
Beilstein Number:0021703
MDL:MFCD00075757
XlogP3-AA:1.00 (est)
Molecular Weight:215.21593000
Formula:C10 H9 N5 O
BioActivity Summary:listing
NMR Predictor:Predict (works with chrome or firefox)
Category:cosmetic ingredient for skin conditioning
 
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
Melting Point: 266.50 °C. @ 760.00 mm Hg
Boiling Point: 524.40 °C. @ 760.00 mm Hg (est)
Flash Point: 520.00 °F. TCC ( 270.90 °C. ) (est)
logP (o/w): 1.200 (est)
Soluble in:
 water, 1.124e+004 mg/L @ 25 °C (est)
 
Organoleptic Properties:
Odor and/or flavor descriptions from others (if found).
 
Cosmetic Information:
CosIng:cosmetic data
Cosmetic Uses: skin conditioning
 
Suppliers:
Alfa Biotechnology
For experimental / research use only.
Kinetin 98%
BOC Sciences
For experimental / research use only.
Kinetin >98%
Odor: characteristic
Use: Kinetin is a type of cytokinin, a class of plant hormone that promotes cell division.
Glentham Life Sciences
Kinetin
Jiangyin Healthway
Kinetin
New functional food ingredients
Sigma-Aldrich: Sigma
For experimental / research use only.
Kinetin ≥99.0% (HPLC)
TCI AMERICA
For experimental / research use only.
Kinetin >99.0%(HPLC)(T)
 
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 450 mg/kg
Nippon Yakurigaku Zasshi. Japanese Journal of Pharmacology. Vol. 61(2), Pg. 43S, 1965.

Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
 
Safety in Use Information:
Category:
cosmetic ingredient for skin conditioning
Recommendation for kinetin usage levels up to:
 not for fragrance use.
 
Recommendation for kinetin flavor usage levels up to:
 not for flavor use.
 
Safety References:
EPI System: View
ClinicalTrials.gov:search
Daily Med:search
Cancer Citations:Search
Toxicology Citations:Search
EPA Substance Registry Services (TSCA):525-79-1
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :3830
National Institute of Allergy and Infectious Diseases:Data
WGK Germany:3
N-(furan-2-ylmethyl)-7H-purin-6-amine
Chemidplus:0000525791
RTECS:AU6270000 for cas# 525-79-1
 
References:
 N-(furan-2-ylmethyl)-7H-purin-6-amine
NIST Chemistry WebBook:Search Inchi
Canada Domestic Sub. List:525-79-1
Pubchem (cid):3830
Pubchem (sid):135020172
 
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):C08272
HMDB (The Human Metabolome Database):HMDB12245
FooDB:FDB028887
Export Tariff Code:2933.99.8290
VCF-Online:VCF Volatile Compounds in Food
ChemSpider:View
Wikipedia:View
EFSA Update of results on the monitoring of furan levels in food:Read Report
EFSA Previous report: Results on the monitoring of furan levels in food:Read Report
EFSA Report of the CONTAM Panel on provisional findings on furan in food:Read Report
Formulations/Preparations:
•liquid concentrate •other products mixtures: cytoplex hms (+4-indol-3-ylbutyric acid + gibberellic acid), green sol 48 (+ gibberellic acid). •trade names: x-cyte; x-cyto •trade names: cytex, nitrozyme, cytogen, and burst yield booster •manufacturing products: form not identifiedliquid- 0.01 to 0.01%; soluble concentrateliquid- 0.0040 to 0.0120%. end use products: flowable concentrate- 0.004 to 0.0096%; liquid-ready to use- 0.00008 to 0.00008%; soluble concentrateliquid- 0.0003 to 0.0400%.
 
Potential Blenders and core components note
None Found
 
Potential Uses:
None Found
 
Occurrence (nature, food, other):note
 found in nature
 
Synonyms:
 adenine, N-furfuryl-
 cytokinin
6-[(fur-2-ylmethyl)amino]purine
N-(furan-2-ylmethyl)-1H-purin-6-amine
N-(furan-2-ylmethyl)-7H-purin-6-amine
N-(furan-2-ylmethyl)-9H-purin-6-amine
6-[(furan-2-ylmethyl)amino]-9H-purine
2-furanmethanamine, N-1H-purin-6-yl-
N-(2-furanyl methyl)-1H-purin-6-amine
N-(2-furanylmethyl)-1H-purin-6-amine
N-furfuryl adenine
N6-furfuryl adenine
6-(furfuryl amino) purine
 furfuryl(purin-6-yl) amine
 furfuryl(purin-6-yl)amine
6-furfuryladenine
N-furfuryladenine
6-(furfurylamino)purine
6-furfurylaminopurine
N-(2-furylmethyl)-1H-purin-6-amine
N-(2-furylmethyl)-3H-purin-6-amine
N-(2-furylmethyl)-7H-purin-6-amine
N-(2-furylmethyl)-9H-purin-6-amine
(2-furylmethyl)purin-6-ylamine
7H-purin-6-amine, N-(2-furanylmethyl)-
N-1H-purin-6-yl-2-furan methanamine
 

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Notes:
a furanyl adenine found in plants and fungi. it has plant growth regulation effects. Kinetin can react with UDP-D-glucose to produce kinetin-7-N-glucoside or kinetin-9-N-glucoside, with UDP as a byproduct. The reaction is catalyzed by UDP glycosyltransferase. Kinetin is a hormone derived from plants. [HMDB]
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