700-06-1 MSDS - Indole-3-carbinol
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Indole-3-carbinol

Identification
Name Indole-3-carbinol
CAS Registry Number 700-06-1
Synonyms 3-indolylcarbinol;I3C;INDOLE-3-METHANOL;INDOLE-3-CARBINOL;INDOLE-3-CARBINOLE;AKOS NCG1-0099;3-HYDROXYMETHYLINDOLE;3-HYDROXYINDOLE
Molecular Structure Indole-3-carbinol   700-06-1
Molecular Formula C9H9NO
Molecular Weight 147.17
mp: 96-99 ℃(lit.)
Hazard Codes: Details
Risk Statements: 36/38
Safety Statements: 26-36
Supplier
Lightchem Inc
Supply Precious metal catalyst
OLED Materials etc.
www.lightchem.com
 
Wiki & MSDS
700-06-1.pdf
Indole-3-carbinol[1]
Indole-3-carbinol.png
Names
IUPAC name
1H-Indol-3-ylmethanol
Other names
Indole-3-carbinol; 3-Indolylcarbinol; 1H-Indole-3-methanol; 3-Hydroxymethylindole; 3-Indolemethanol; Indole-3-methanol; I3C
Identifiers
CAS Number
  • 700-06-1 YesY
3D model (Jmol)
  • Interactive image
ChEBI
  • CHEBI:24814 YesY
ChemSpider
  • 3581 YesY
ECHA InfoCard 100.010.762
EC Number 211-836-2
PubChem CID
  • 3712
RTECS number NL9483000
Properties
Chemical formula
C9H9NO
Molar mass 147.18 g·mol−1
Appearance Off-white solid
Melting point 96 to 99 °C (205 to 210 °F; 369 to 372 K)
Solubility in water
Partially in cold water[vague]
Hazards
EU classification (DSD)
Irritating (Xi)
R-phrases R36/38
S-phrases S26, S36
NFPA 704
Flammability code 0: Will not burn. E.g., waterHealth code 1: Exposure would cause irritation but only minor residual injury. E.g., turpentineReactivity code 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g., liquid nitrogenSpecial hazards (white): no codeNFPA 704 four-colored diamond
0
1
0
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
YesY verify (what is YesYN ?)
Infobox references

Indole-3-carbinol (C9H9NO) is produced by the breakdown of the glucosinolate glucobrassicin, which can be found at relatively high levels in cruciferous vegetables such as broccoli, cabbage, cauliflower, brussels sprouts, collard greens and kale. It is also available in dietary supplements.[2] Indole-3-carbinol is the subject of on-going biomedical research into its possible anticarcinogenic,[3] antioxidant, and anti-atherogenic effects.[4] Research on indole-3-carbinol has been conducted primarily using laboratory animals and cultured cells.[5] Limited and inconclusive human studies have been reported. A recent review of the biomedical research literature found that "evidence of an inverse association between cruciferous vegetable intake and breast or prostate cancer in humans is limited and inconsistent" and "larger randomized controlled trials are needed" to determine if supplemental indole-3-carbinol has health benefits.[6]


 







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