2-indanone
2H-inden-2-one, 1,3-dihydro-
 
Notes:
None found
  • BOC Sciences
    • BOC Sciences
      Best of Chemicals Supplier
      Quality supplier of research chemicals and biochemicals including inhibitors, building blocks, GMP Products, impurities and metabolites, APIs for Veterinary, Natural Compounds, ADCs, Stem Cell Molecule and chiral compounds.
      BOC Sciences provides a wide range of services to support the pharmaceutical industry through all stages of drug discovery including Custom Synthesis of those chemicals that are not in stock, Isotope Labeling Service, Chiral Synthesis and Resolution, Bioconjugation, PEGylation services, analytical services.
      BOC Sciences is a brand of BOCSCI Inc. We leverage our wide spectrum of business in the fields of development, manufacturing, marketing, and distribution to help you make best-informed decisions tailored to your evolving needs for premium chemicals. Our complete suite of CRO services spans the entire molecule development pipeline including contract research for target identification, building blocks, compound synthesis, biochemical and cellular analysis, preclinical animal tests, and clinical studies.
      Email: Marketing
      US Email: Marketing
      Email: Sales
      US Email: Sales
      Voice: 1-631-485-4226
      Fax: 1-631-614-7828
      US Voice: 1-631-485-4226
      US Fax: 1-631-614-7828
      Europe44-203-286-1088
      Facebook
      Twitter
      Linkedin
      Blog
      Get the App!
      Product(s):
      615-13-4 2-Indanone 98%
       
  • 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):
      I0649 2-Indanone >98.0%(GC)
       
Synonyms   Articles   Notes   Search
CAS Number: 615-13-4Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg: 210-410-3
FDA UNII: 0I79N673DE
Nikkaji Web: J7.027K
Beilstein Number: 0636550
MDL: MFCD00003792
XlogP3-AA: 1.30 (est)
Molecular Weight: 132.16196000
Formula: C9 H8 O
BioActivity Summary: listing
NMR Predictor: Predict (works with chrome or firefox)
Category: fragrance agents
 
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
Perfumer and Flavorist: Search
Google Patents: Search
US Patents: Search
EU Patents: Search
Pubchem Patents: Search
PubMed: Search
NCBI: Search
Synonyms   Articles   Notes   Search   Top
Physical Properties:
Assay: 95.00 to 100.00 % 
Food Chemicals Codex Listed: No
Melting Point: 59.00 °C. @ 760.00 mm Hg
Boiling Point: 248.90 °C. @ 760.00 mm Hg (est)
Flash Point: 212.00 °F. TCC ( 100.00 °C. )
logP (o/w): 1.230 (est)
Soluble in:
 water, 5561 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:
BOC Sciences
For experimental / research use only.
2-Indanone 98%
EMD Millipore
For experimental / research use only.
2-Indanone
Santa Cruz Biotechnology
For experimental / research use only.
2-Indanone
Sigma-Aldrich: Aldrich
For experimental / research use only.
2-Indanone 98%
TCI AMERICA
For experimental / research use only.
2-Indanone >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:
intravenous-mouse LD50  56 mg/kg
U.S. Army Armament Research & Development Command, Chemical Systems Laboratory, NIOSH Exchange Chemicals. Vol. NX#08390

Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
Synonyms   Articles   Notes   Search   Top
Safety in Use Information:
Category: fragrance agents
RIFM Fragrance Material Safety Assessment: Search
IFRA Code of Practice Notification of the 49th Amendment to the IFRA Code of Practice
 
Recommendation for 2-indanone flavor usage levels up to:
 not for flavor use.
Synonyms   Articles   Notes   Search   Top
Safety References:
EPI System: View
AIDS Citations: Search
Cancer Citations: Search
Toxicology Citations: Search
EPA Substance Registry Services (TSCA): 615-13-4
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 11983
National Institute of Allergy and Infectious Diseases: Data
WGK Germany: 3
 1,3-dihydroinden-2-one
Chemidplus: 0000615134
RTECS: NK7535500 for cas# 615-13-4
Synonyms   Articles   Notes   Search   Top
References:
 1,3-dihydroinden-2-one
NIST Chemistry WebBook: Search Inchi
Canada Domestic Sub. List: 615-13-4
Pubchem (cid): 11983
Pubchem (sid): 134977294
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
Metabolomics Database: Search
UM BBD: Search
KEGG (GenomeNet): C07727
HMDB (The Human Metabolome Database): Search
Export Tariff Code: 2914.39.9000
ChemSpider: View
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
 not found in nature
Synonyms   Articles   Notes   Search   Top
Synonyms:
2,3-dihydro-1H-inden-2-one
1,3-dihydro-2H-inden-2-one
1,3-dihydroinden-2-one
 indan-2-one
2H-inden-2-one, 1,3-dihydro-
1H-inden-2(3H)-one
Synonyms   Articles   Notes   Search   Top
Articles:
PubMed: Bromoform activation. TiCl4-Mg-promoted CHBr2- and CBr3- transfer to a variety of aldehydes and ketones.
PubMed: Synthesis of indenoporphyrins, highly modified porphyrins with reduced diatropic characteristics.
PubMed: Diastereoisomers of 2-benzyl-2, 3-dihydro-2-(1H-inden-2-yl)-1H-inden-1-ol: potential anti-inflammatory agents.
PubMed: Exploring the reactivity of a coordinatively unsaturated Cp*Ru(kappa(2)-P,O) complex with small molecule substrates: application in E-H bond activation (E = H, B, and Si).
PubMed: Calorimetric and computational study of indanones.
PubMed: Experimental study on the thermal oxidation of 2-chlorophenol in air over the temperature range 450-900 degrees C.
PubMed: Aromatic and aliphatic hydrocarbon consumption and transformation by the styrene degrading strain Pseudomonas putida CA-3.
PubMed: Lipoprotein mutation accelerates substrate permeability-limited toluene dioxygenase-catalyzed reaction.
PubMed: Transition-state effects in acid-catalyzed aryl epoxide hydrolyses.
PubMed: Syntheses of 2-substituted indoles and fused indoles by photostimulated reactions of o-iodoanilines with carbanions by the SRN1 mechanism.
PubMed: Synthesis of 2-indanones via [4 + 1] annulation reactions of (trialkylsilyl)arylketenes.
PubMed: Unusual reactions of 5,5-dimethyl-2-(indenyl-2)-3-pyrazolidinone with acetylenedicarboxylates
PubMed: Pronounced differences in inhibition potency of lactone and non-lactone compounds for mouse and human coumarin 7-hydroxylases (CYP2A5 and CYP2A6).
PubMed: New metabolites in the degradation of fluorene by Arthrobacter sp. strain F101.
PubMed: Regiospecific and stereoselective hydroxylation of 1-indanone and 2-indanone by naphthalene dioxygenase and toluene dioxygenase.
PubMed: Regiospecific and stereoselective hydroxylation of 1-indanone and 2-indanone by naphthalene dioxygenase and toluene dioxygenase.
PubMed: Metabolism and nephrotoxicity of indan in male Fischer 344 rats.
PubMed: Gas chromatographic/mass spectrometric studies of the urinary metabolites of male rats given indan.
Synonyms   Articles   Notes   Search   Top
Please share your Comments.
Email Address:
 
 
 
 
Top of Page Home
Copyright © 1980-2021 Perflavory ™ Disclaimer Privacy Policy