| Weight | 131.178 g/mol |
|---|---|
| Formula | C9H9N |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 0 |
3-METHYLINDOLE (83-34-1)
Skatole · 3 Methylindole
Score:
#2139 in Biology
,
#2628 in Chemistry
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- Physiological aspects of androstenone and skatole formation in the boar-A review with experimental data. (Meat Science, 1994)
- Microbial production of skatole in the hind gut of pigs given different diets and its relation to skatole deposition in backfat (Animal Science, 1995)
- Microbial metabolites of tryptophan in the intestinal tract with special reference to skatole. (The American Journal of Clinical Nutrition, 1979)
- [34] Modification of tryptophan with BNPS-skatole (2-(2-nitrophenylsulfenyl)-3-methyl-3-bromoindolenine) (Methods in Enzymology, 1972)
- Near-ultraviolet absorption bands of tryptophan. Studies using indole and 3-methylindole as models. (Biochemistry, 1970)
- 3-Methylindole (Skatole) and Indole Production by Mixed Populations of Pig Fecal Bacteria (Applied and Environmental Microbiology, 1995)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Skatole
- 3 Methylindole
-
SMILESCC1=CNC2=CC=CC=C12
-
InChIKeyZFRKQXVRDFCRJG-UHFFFAOYSA-N
- Pubchem - 3-METHYLINDOLE
- Wikipedia - skatole
Skatole or 3-methylindole is a mildly toxic white crystalline organic compound belonging to the indole family. It occurs naturally in feces (it is produced from tryptophan in the mammalian digestive tract) and coal tar and has a strong fecal odor. In low concentrations, it has a flowery smell and is found in several flowers and essential oils, including those of orange blossoms, jasmine, and Ziziphus mauritiana.
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3-METHYLINDOLE
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