| Identification | More | [Name]
3-Methylindole | [CAS]
83-34-1 | [Synonyms]
3-METHYL-1H-INDOLE
3-METHYLINDOLE
3-MI
BETA-METHYLINDOLE
FEMA 3019
SCATOLE
SKATOL
SKATOLE
SKETOLE
1H-Indole,3-methyl-
3-methyl-1h-indol
3-methyl-indol
3-Methylindole (skatole)
Indole, 3-methyl-
skatole(3-methylindole)
SKATOLE 98+%
3-Methylindole,~99%
skatole,3-methyl-1H-indole
3-METLYLINDOLE
SKATOLE(RG) | [EINECS(EC#)]
201-471-7 | [Molecular Formula]
C9H9N | [MDL Number]
MFCD00005627 | [Molecular Weight]
131.17 | [MOL File]
83-34-1.mol |
| Chemical Properties | Back Directory | [Appearance]
slightly brown platelets | [Melting point ]
92-97 °C (lit.) | [Boiling point ]
265-266 °C (lit.) | [density ]
1.0111 (estimate) | [FEMA ]
3019 | [refractive index ]
1.6070 (estimate) | [Fp ]
132 °C
| [storage temp. ]
Store below +30°C. | [solubility ]
Chloroform (Slightly), Methanol (Slightly) | [form ]
Crystalline Powder or Flakes | [pka]
17.30±0.30(Predicted) | [color ]
Almost white to pale brown | [Odor]
indole-like odor | [Stability:]
Stable, but light-sensistive. Stench! Incompatible with strong oxidizing agents, strong acids, acid ahydrides, acid chlorides. Combustible. | [Odor Threshold]
0.0000056ppm | [Odor Type]
animal | [Water Solubility ]
Soluble in water, Ether, Alcohols, Benzene, Acetone, Chloroform. | [Sensitive ]
Light Sensitive | [Usage]
A highly fluorescent guanosine analogue, which in a dimethoxytrityl, phosphoramidite protected form, can be site-specifically inserted into oligonucleotides through a 3?5?phosphodiester linkage using an automated DNA synthesizer | [Detection Methods]
HPLC,NMR | [JECFA Number]
1304 | [Merck ]
14,8560 | [BRN ]
111296 | [InChIKey]
ZFRKQXVRDFCRJG-UHFFFAOYSA-N | [LogP]
2.60 | [CAS DataBase Reference]
83-34-1(CAS DataBase Reference) | [NIST Chemistry Reference]
1H-Indole, 3-methyl-(83-34-1) | [Storage Precautions]
Light sensitive | [EPA Substance Registry System]
83-34-1(EPA Substance) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing . | [RIDADR ]
UN3077 - class 9 - PG 3 - DOT/IATA UN3335 - Environmentally hazardous substances, solid, n.o.s., HI: all (not BR) | [WGK Germany ]
2
| [RTECS ]
NM0350000
| [F ]
8-13 | [TSCA ]
Yes | [HS Code ]
29339920 | [Safety Profile]
Poison by ingestion,
intravenous, and intraperitoneal routes.
Moderately toxic by subcutaneous route.
When heated to decomposition it emits
toxic fumes of NOx. | [Hazardous Substances Data]
83-34-1(Hazardous Substances Data) | [Toxicity]
MLD in frogs (mg/kg): 1000 s.c. (Bin-Ichi) |
| Hazard Information | Back Directory | [Chemical Properties]
Skatole has a characteristic putrid, fecal odor at high concentrations, becoming pleasant, jasmine-like, fruity sweet, warm at very low concentrations. It has a warm overripe fruity flavor below 1 ppm. | [Physical properties]
White crystals or slightly brown platelets. soluble in 3 volumes of 95% ethanol and oily fragrance. 3-Methylindole has a salty and strong indole-like animal fragrance, which is very powerful, has strong diffusion and is very durable. The smell at high concentrations is disgusting, only at very low concentrations there is a large civet-like animal aroma, and the taste is warm and overripe fruit-like. | [Occurrence]
Reported found in beetroot, feces, coal tar, Swiss cheese, Gruyere cheese, mozarella cheese, butter, milk, goat and sheep milk, boiled egg, fatty fish, coffee, tea, trassi, rice bran, dried bonito and squid. | [Uses]
3-Methylindole is a naturally abundant pneumotoxin, found primarily in mammalian feces providing its strong fecal odor. In lower concentrations however, the compound has a pleasent aroma, giving orange blossoms and ja smine their pleasing scent. It is often a component of commercial fragrances and perfumes.It helps fluorescent guanosine analogue, which in a dimethoxytrityl, phosphoramidite protected form, can be site-specifically inserted into oligonucleotides through a 3'-5' phosphodiester linkage using an automated DNA synthesizer. | [Definition]
ChEBI: A methylindole carrying a methyl substituent at position 3. It is produced during the anoxic metabolism of L-tryptophan in the mammalian digestive tract. | [Preparation]
Prepared synthetically from the phenylhydrazone of propionaldehyde or by cyclization of o-toluidides (Bedoukian, 1967). | [Aroma threshold values]
Detection: 0.2 ppb | [Synthesis Reference(s)]
Journal of the American Chemical Society, 99, p. 3532, 1977 DOI: 10.1021/ja00452a073
The Journal of Organic Chemistry, 45, p. 2709, 1980 DOI: 10.1021/jo01301a032
Tetrahedron Letters, 28, p. 5291, 1987 DOI: 10.1016/S0040-4039(00)96710-8 | [General Description]
3-Methylindole (3-MI), commonly found in wine, dairy products, and other foodstuffs, leads to an unpleasant fecal like odor in pig meat products. It is reported to be produced in the intestines of several species by the microbial degradation of tryptophan. | [Pharmacology]
Skatole (l00mg dissolved in 2 ml sesame oil administered by gastric intubation)
failed to prevent apoplexy in the adrenals of rats when administered 24 hr before injection of 5 mg
of 7,12-dimethylbenz[a]anthracene (Huggins & Fukunishi, 1964).
In rat costal cartilage, skatole inhibited 35SO42-incorporation into chondroitin sulphate and 14C-labelled proline incorporation into protein (Liberti & Rogers, 1970). In concentrations of 5-10 mM, it inhibited oxygen uptake in slices of rat liver and rat-brain cortex (Lascelles & Taylor, 1968; Walshe et al. 1958). Skatole has also shown depressant (catatonic-like) activity on the swimming behaviour of guppies and the exploratory behaviour of rats (Sprince, 1969). When injected ip, 1 mmol/kg did not have any radioprotective effect in mice, the survival effect (ratio of mean survival time in a treated group to that of the control in 30 days after irradiation) being 0.97
or 0.70 when skatole was administered 30 or 5 min, respectively, before X-irradiation with 800 R
(Shinoda et al 1974).
Skatole (1.0mM) caused >50% inhibition of the anaphylactic release of histamine from chopped,
sensitized guinea-pig lung by chymotrypsin substrates and inhibitors (Austen & Brocklehurst, 1961).
It had a non-specific excitatory action on the heart of the marine mollusc Venus mercenaria (Greenberg,
1960) and in a 194 μM concentration produced half-maximal positive inotropic activity in
isolated left guinea-pig atria (Zetler, 1974). | [Toxicology]
3-Methylindole (3MI), an abnormal metabolite of tryptophan, causes acute pulmonary edema and emphysema. 3MI toxicity is species-, tissue- and cell-specific and is an excellent model for understanding the processes of chemically-induced lung injury. This 3-methylindole (3-MI) is absorbed through the rumen wall and circulated around the body. The 3-MI is toxic to the primary cells that line the interior surface of the lungs. Thus, as the high levels of 3-MI move from the rumen to the lungs more and more lung tissue is destroyed.
Toxicity of 3-Methyleneoxindole, a Proposed Reactive Intermediate in the Metabolism of 3-Methylindole
The metabolic basis of 3-methylindole-induced pneumotoxicity
Association of 3-methyleneindolenine, a toxic metabolite of 3-methylindole, with acute interstitial pneumonia in feedlot cattle
Mechanisms of 3-methylindole pneumotoxicity | [Synthesis]
Indoles (skatole) with various substituents in the 2 and 3 position can be synthesized via the Fisher indole synthesis, which involves two steps and utilizes a phenylhydrazine and an aliphatic or aromatic aldehyde or ketone as starting materials. | [Metabolic pathway]
Three major metabolites of 14C-skatole are found in
the plasma/urine of pigs given skatole and are
identified as 6-sulfatoxyskatole, 3-hydroxy-3-
methyloxindole, and the mercapturate adduct of
skatole, 3-[(N-acetylcysteine-S-yl)methyl]indole. For
other pathways, see the references in the text. | [Metabolism]
3-Methylindole (skatole) has been reported by several authors to be excreted as an ethereal sulphate by dogs, rats and man; distillation of the urine results in the formation of indole, which might well be derived by decarboxylation of indolyl-3-carboxylic acid, an expected oxidation product of skatole (Williams, 1959). Oral administration of skatole to rats resulted in the urinary excretion of a mixture of sulphate esters of hydroxyskatoles (Dalgliesh, Kelly & Horning, 1958; Horning, Sweeley, Dalgliesh & Kelly, 1959). The faeces of rats fed a chow diet were found to contain typtophan metabolites, including up to 0.78 ?g skatole/g wet faeces (Anderson, 1975). Metabolites of skatole were detected in the urine of a human subject fed skatole (Sano & Miyanoki, 1955). In man, skatole has been shown to undergo hydroxylation mainly at position 6. In rats and man, 6-hydroxyskatole is excreted chiefly as the sulphate (Horning et al. 1959), but it may also be excreted as the glucuronide (Sohler, 1966). The metabolites of skatole excreted in the urine of man and 16 species of domestic and wild mammals were also studied by Decker & Gerdemann (1959). After administration of skatole to cattle in a dose of 0.1-0.2 g skatole/kg intraruminally or 0.06g/kg by jugular infusion, the mean plasma concentration of skatole became maximal at 3 and 9hr, respectively (Carlson et al. 1975). | [storage]
Store at -20°C | [Purification Methods]
Crystallise skatole from *benzene or pet ether (m 96.5o). It has also been purified by zone melting. The picrate has m 182o (from Et2O or Et2O/MeOH). [Beilstein 20 III/IV 3206, 20/7 V 69.] |
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