trans-stilbene
benzene, 1,1'-(1,2-ethenediyl)bis-, (E)- (9CI)
 
Notes:
None found
  • TCI AMERICA
    • TCI AMERICA
      Moving Your Chemistry Forward
      We continuously strive to advance our technology.
      With East & West Coast distribution centers, count on TCI to deliver products quickly and reliably. Over 30,000 Reagents available today in benchtop to bulk quantities. We also offer custom synthesis solutions. Sign up for a TCI account today for fast and free shipping!
      Tokyo Chemical Industry Co., Ltd. (TCI) is a leading worldwide manufacturer of specialty organic chemicals founded in 1946. TCI provides organic laboratory chemicals as well as pharmaceutical, cosmetic and functional materials. More than 70 years of synthesis experience and multi-purpose plants enable TCI to offer more than 30,000 products as well as custom synthesis.
      US Email: Sales
      Email: Technical Support
      Voice: 1-800-423-8616
      Fax: 1- 888-520-1075
      Facebook
      Twitter
      Instagram
      Linkedin
      Product(s):
      S0090 trans-Stilbene >98.0%(GC)
       
Synonyms   Articles   Notes   Search
CAS Number: 103-30-0Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg: 203-098-5
FDA UNII: 3FA7NW80A0
Nikkaji Web: J46.982C
Beilstein Number: 1616740
MDL: MFCD00064300
XlogP3: 4.80 (est)
Molecular Weight: 180.24964000
Formula: C14 H12
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
Synonyms   Articles   Notes   Search   Top
Physical Properties:
Appearance: white crystals (est)
Assay: 95.00 to 100.00 % 
Food Chemicals Codex Listed: No
Specific Gravity: 0.97000 @  25.00 °C.
Melting Point: 123.00 °C. @ 760.00 mm Hg
Boiling Point: 307.00 °C. @ 760.00 mm Hg
Flash Point: 263.00 °F. TCC ( 128.50 °C. ) (est)
logP (o/w): 4.810
Soluble in:
 water, 0.29 mg/L @ 25 °C (exp)
 water, 4.285 mg/L @ 25 °C (est)
Synonyms   Articles   Notes   Search   Top
Organoleptic Properties:
 
Odor and/or flavor descriptions from others (if found).
 
 
Synonyms   Articles   Notes   Search   Top
Cosmetic Information:
None found
Synonyms   Articles   Notes   Search   Top
Suppliers:
EMD Millipore
For experimental / research use only.
trans-Stilbene
Santa Cruz Biotechnology
For experimental / research use only.
trans-Stilbene ≥96%
Sigma-Aldrich: Aldrich
For experimental / research use only.
trans-Stilbene 96%
TCI AMERICA
For experimental / research use only.
trans-Stilbene >98.0%(GC)
Synonyms   Articles   Notes   Search   Top
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  6500 mg/kg
Yaoxue Xuebao. Acta Pharmaceutica Sinica. Pharmaceutical Journal. Vol. 14, Pg. 227, 1979.

oral-mouse LD50  920 mg/kg
Yaoxue Xuebao. Acta Pharmaceutica Sinica. Pharmaceutical Journal. Vol. 14, Pg. 227, 1979.

Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
Synonyms   Articles   Notes   Search   Top
Safety in Use Information:
Category: natural substances and extractives
Recommendation for trans-stilbene usage levels up to:
 not for fragrance use.
 
Recommendation for trans-stilbene flavor usage levels up to:
 not for flavor use.
Synonyms   Articles   Notes   Search   Top
Safety References:
EPI System: View
Chemical Carcinogenesis Research Information System: Search
AIDS Citations: Search
Cancer Citations: Search
Toxicology Citations: Search
EPA GENetic TOXicology: Search
EPA Substance Registry Services (TSCA): 103-30-0
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 638088
National Institute of Allergy and Infectious Diseases: Data
WGK Germany: 2
 (E)-stilbene
Chemidplus: 0000103300
EPA/NOAA CAMEO: hazardous materials
RTECS: WJ4926500 for cas# 103-30-0
Synonyms   Articles   Notes   Search   Top
References:
 (E)-stilbene
NIST Chemistry WebBook: Search Inchi
Canada Domestic Sub. List: 103-30-0
Pubchem (cid): 638088
Pubchem (sid): 135024534
Synonyms   Articles   Notes   Search   Top
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
HMDB (The Human Metabolome Database): Search
Export Tariff Code: 2902.90.9000
VCF-Online: VCF Volatile Compounds in Food
ChemSpider: View
Wikipedia: View
Formulations/Preparations:
grades: technical; pure.
Synonyms   Articles   Notes   Search   Top
Potential Blenders and core components note
 
None Found
 
Synonyms   Articles   Notes   Search   Top
Potential Uses:
None Found
Synonyms   Articles   Notes   Search   Top
Occurrence (nature, food, other): note
 petiveria alliacea root
Search Trop  Picture
Synonyms   Articles   Notes   Search   Top
Synonyms:
 benzene, 1,1'- (1,2-ethenediyl)bis-, (E)-
 benzene, 1,1'-(1,2-ethenediyl)bis-, (E)- (9CI)
 benzene, 1,1'-(1E)-1,2-ethenediylbis-
 benzene, 1,1'-[(E)-1,2-ethenediyl]bis-
trans-bibenzylidene
 dibenzal, (E)-
 dibenzylidne, (E)-
(E)-1,2-diphenyl ethylene
trans-1,2-diphenyl ethylene
(E)-1,2-diphenylethene
1,trans-2-diphenylethene
trans-diphenylethene
trans-1,2-diphenylethene
1,2-diphenylethene, (E)-
(E)-1,2-diphenylethylene
1,trans-2-diphenylethylene
trans-1,2-diphenylethylene
trans-a,b-diphenylethylene
1,2-diphenylethylene (trans)
1,2-diphenylethylene, trans
1,1'-(1,2-ethanediyl)bis(benzene), (E)-
1,1'-(1,2-ethanediyl)bis[benzene], trans
1,1'-(E)-ethen-1,2-diyldibenzol
1,1'-[(E)-1,2-ethendiyl]dibenzol
(E)-1,1'-(1,2-ethene diyl) bisbenzene
1,1'-[(1E)-ethene-1,2-diyl]dibenzene
1,1'-(E)-ethene-1,2-diyldibenzene
(1,2-ethenediyl)-1,1'-bisbenzene, (E)-
(E)-1,1'-(1,2-ethenediyl)bisbenzene
1,1'-[(E)-1,2-ethenediyl]dibenzene
((E)-2-phenylethenyl)benzene
[(E)-2-phenylethenyl]benzene
((1E)-2-phenylvinyl)benzene
(E)-stilbene
 stilbene, (E)-
Synonyms   Articles   Notes   Search   Top
Articles:
PubMed: Toward an understanding of the role of a catechol moiety in cancer chemoprevention: The case of copper- and o-quinone-dependent Nrf2 activation by a catechol-type resveratrol analog.
PubMed: Resveratrol and cardiovascular health--promising therapeutic or hopeless illusion?
PubMed: Preparation of chitosan-TPP microspheres as resveratrol carriers.
PubMed: Resveratrol down-regulates a glutamate-induced tissue plasminogen activator via Erk and AMPK/mTOR pathways in rat primary cortical neurons.
PubMed: Stilbene analogs of resveratrol improve insulin resistance through activation of AMPK.
PubMed: In vivo and in vitro metabolism of trans-resveratrol by human gut microbiota.
PubMed: Resveratrol affects differently rat liver and brain mitochondrial bioenergetics and oxidative stress in vitro: investigation of the role of gender.
PubMed: Anti-obesity effect of resveratrol-amplified grape skin extracts on 3T3-L1 adipocytes differentiation.
PubMed: Piceatannol suppresses breast cancer cell invasion through the inhibition of MMP-9: involvement of PI3K/AKT and NF-κB pathways.
PubMed: A combination of resveratrol and melatonin exerts chemopreventive effects in N-methyl-N-nitrosourea-induced rat mammary carcinogenesis.
PubMed: 3,4,4'-Trihydroxy-trans-stilbene, an analogue of resveratrol, is a potent antioxidant and cytotoxic agent.
PubMed: Resveratrol derivatives as promising chemopreventive agents with improved potency and selectivity.
PubMed: Structure-activity relationship of resveratrol and its analogue, 4,4'-dihydroxy-trans-stilbene, toward the endothelin axis in human endothelial cells.
PubMed: Extract of passion fruit (Passiflora edulis) seed containing high amounts of piceatannol inhibits melanogenesis and promotes collagen synthesis.
PubMed: Evaluation of anti-invasion effect of resveratrol and related methoxy analogues on human hepatocarcinoma cells.
PubMed: Physicochemical study of the complexation of pterostilbene by natural and modified cyclodextrins.
PubMed: Mechanisms of apoptotic effects induced by resveratrol, dibenzoylmethane, and their analogues on human lung carcinoma cells.
PubMed: Resveratrol analog-3,5,4'-trimethoxy-trans-stilbene inhibits invasion of human lung adenocarcinoma cells by suppressing the MAPK pathway and decreasing matrix metalloproteinase-2 expression.
PubMed: Structure-activity relationship and mechanism of the tocopherol-regenerating activity of resveratrol and its analogues.
PubMed: Thiomethylstilbenes as inhibitors of CYP1A1, CYP1A2 and CYP1B1 activities.
PubMed: The grape and wine constituent piceatannol inhibits proliferation of human bladder cancer cells via blocking cell cycle progression and inducing Fas/membrane bound Fas ligand-mediated apoptotic pathway.
PubMed: Antidiabetic properties of 2,5-dihydroxy-4,3'-di(beta-D-glucopyranosyloxy)-trans-stilbene from mulberry (Morus bombycis koidzumi) root in streptozotocin-induced diabetic rats.
PubMed: A pilot study of evaluation of the antioxidative activity of resveratrol and its analogue in a 6-month feeding test in young adult mice.
PubMed: Myricetin down-regulates phorbol ester-induced cyclooxygenase-2 expression in mouse epidermal cells by blocking activation of nuclear factor kappa B.
PubMed: Oncogenicity evaluation of resveratrol in p53(+/-) (p53 knockout) mice.
PubMed: Antioxidant activity and inhibition of alpha-glucosidase by trans-resveratrol, piceid, and a novel trans-stilbene from the roots of Israeli Rumex bucephalophorus L.
PubMed: Structural basis for DNA-cleaving activity of resveratrol in the presence of Cu(II).
PubMed: Molecular mechanisms of the chemopreventive effects of resveratrol and its analogs in carcinogenesis.
PubMed: Metabolism and bioavailability of trans-resveratrol.
PubMed: A methoxy derivative of resveratrol analogue selectively induced activation of the mitochondrial apoptotic pathway in transformed fibroblasts.
PubMed: Structural basis for antioxidant activity of trans-resveratrol: ab initio calculations and crystal and molecular structure.
PubMed: The grape and wine polyphenol piceatannol is a potent inducer of apoptosis in human SK-Mel-28 melanoma cells.
PubMed: Grape polyphenol resveratrol and the related molecule 4-hydroxystilbene induce growth inhibition, apoptosis, S-phase arrest, and upregulation of cyclins A, E, and B1 in human SK-Mel-28 melanoma cells.
PubMed: Synthesis and biological evaluation of resveratrol and analogues as apoptosis-inducing agents.
PubMed: Resveratrol, a natural product derived from grapes, is a new inducer of differentiation in human myeloid leukemias.
PubMed: Mechanism of cardioprotection by resveratrol, a phenolic antioxidant present in red wine (Review).
PubMed: Evaluation of resveratrol derivatives as potential antioxidants and identification of a reaction product of resveratrol and 2, 2-diphenyl-1-picryhydrazyl radical.
PubMed: Fungitoxicity of chemical analogs with heartwood toxins.
PubMed: Epoxide-metabolizing enzymes in mammary gland and liver from BALB/c mice and effects of inducers on enzyme activity.
Synonyms   Articles   Notes   Search   Top
Please share your Comments.
Email Address:
 
 
 
 
Top of Page Home
Copyright © 1980-2021 Perflavory ™ Disclaimer Privacy Policy