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

4-nerolidyl catechol

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CAS Number: 74683-11-7Picture of molecule3D/inchi
FDA UNII: Search
Nikkaji Web:J911.662A
XlogP3-AA:7.00 (est)
Molecular Weight:314.46850000
Formula:C21 H30 O2
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
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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
Soluble in:
 water, 0.007014 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.
4-Nerolidylcatechol > 95%
 
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 4-nerolidyl catechol usage levels up to:
 not for fragrance use.
 
Recommendation for 4-nerolidyl catechol 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 :5352089
National Institute of Allergy and Infectious Diseases:Data
4-[(6E)-3,7,11-trimethyldodeca-1,6,10-trien-3-yl]benzene-1,2-diol
Chemidplus:0074683117
 
References:
 4-[(6E)-3,7,11-trimethyldodeca-1,6,10-trien-3-yl]benzene-1,2-diol
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):5352089
Pubchem (cas):74683-11-7
 
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
HMDB (The Human Metabolome Database):HMDB31924
FooDB:FDB008612
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
 pothomorphe peltata
Search Trop Picture
 pothomorphe umbellata
Search Trop Picture
 
Synonyms:
1,2-benzenediol, 4-(1-ethenyl-1,5,9-trimethyl-4,8-decadienyl)-
4-nerolidylcatechol
4-[(6E)-3,7,11-trimethyldodeca-1,6,10-trien-3-yl]benzene-1,2-diol
 

Articles:

PubMed:4-Nerolidylcatechol: apoptosis by mitochondrial mechanisms with reduction in cyclin D1 at G0/G1 stage of the chronic myelogenous K562 cell line.
PubMed:Liposomal Entrapment of 4-Nerolidylcatechol: Impact on Phospholipid Dynamics, Drug Stability and Bioactivity.
PubMed:4-Nerolidylcatechol analogues as promising anticancer agents.
PubMed:In vivo antimalarial activity and mechanisms of action of 4-nerolidylcatechol derivatives.
PubMed:Anticancer and Anti-Inflammatory Activities of a Standardized Dichloromethane Extract from Piper umbellatum L. Leaves.
PubMed:Antioxidant effect of 4-nerolidylcatechol and α-tocopherol in erythrocyte ghost membranes and phospholipid bilayers.
PubMed:Evaluation of antimicrobial and antimalarial activities of crude extract, fractions and 4-nerolidylcathecol from the aerial parts of Piper umbellata L. (Piperaceae).
PubMed:Pothomorphe umbellata: antifungal activity against strains of Trichophyton rubrum.
PubMed:Antioxidant and cytotoxic effects of crude extract, fractions and 4-nerolidylcathecol from aerial parts of Pothomorphe umbellata L. (Piperaceae).
PubMed:4-Nerolidylcatechol and its synthetic analogues: antioxidant activity and toxicity evaluation.
PubMed:Anti-inflammatory and antinociceptive activities of LQFM002 - A 4-nerolidylcatechol derivative.
PubMed:Stability and antioxidant activity of semi-synthetic derivatives of 4-nerolidylcatechol.
PubMed:Anti-inflammatory effect of (E)-4-(3,7-dimethylocta-2,6-dienylamino)phenol, a new derivative of 4-nerolidylcatechol.
PubMed:Proteasome inhibition and ROS generation by 4-nerolidylcatechol induces melanoma cell death.
PubMed:Impact of ultrasound-assisted extraction on quality and photostability of the Pothomorphe umbellata extracts.
PubMed:In vivo and in vitro antimalarial activity of 4-nerolidylcatechol.
PubMed:Piper peltatum: biomass and 4-nerolidylcatechol production.
PubMed:New antimalarial and cytotoxic 4-nerolidylcatechol derivatives.
PubMed:Apoptosis induction by 4-nerolidylcatechol in melanoma cell lines.
PubMed:Bioactive aristolactams from Piper umbellatum.
PubMed:Dose-dependent in vitro inhibition of rabbit corneal matrix metalloproteinases by an extract of Pothomorphe umbellata after alkali injury.
PubMed:Protective effects of 4-nerolidylcatechol against genotoxicity induced by cyclophosphamide.
PubMed:In vitro inhibition of Plasmodium falciparum by substances isolated from Amazonian antimalarial plants.
PubMed:In vitro and in vivo inhibition of skin matrix metalloproteinases by Pothomorphe umbellata root extract.
PubMed:Chemical stability and SPF determination of Pothomorphe umbellata extract gel and photostability of 4-nerolidylcathecol.
PubMed:Inhibitory effects of Piper umbellatum and Piper peltatum extracts towards myotoxic phospholipases A2 from Bothrops snake venoms: isolation of 4-nerolidylcatechol as active principle.
PubMed:Evaluation of percutaneous absorption of 4-nerolidylcathecol from four topical formulations.
PubMed:Investigation of the larvicidal activity of Pothomorphe peltata and isolation of the active constituent.
PubMed:Cytotoxic 4-nerolidylcatechol from Pothomorphe peltata inhibits topoisomerase I activity.
PubMed:4-Nerolidylcatechol from Pothomorphe spp. scavenges peroxyl radicals and inhibits Fe(II)-dependent DNA damage.
 
Notes:
None found
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