Product Name: |
III, Methylindole |
CAS: |
83-34-1 |
MF: |
C9H9N |
MW: |
131.17 |
EINECS: |
201-471-7 |
Mol File: |
83-34-1.mol |
|
Liquescens punctum |
92-97 ° C (Litt.) |
Ferveret |
265-266 ° C (Litt.) |
density |
1.0111 (estimate) |
potenti |
MMMXIX | SKATOLE |
refractiveindex |
1.6070 (estimate) |
Fp |
CXXXII ° F |
storagetemp. |
+ Copia infra XXX ° F. |
pka |
17.30 ± 0,30 (Praedicta) |
forma |
Vel crystallinum pulveris Flakes |
color |
Fere albus |
Odor |
sicut odor indole, |
OdorThreshold |
0.0000056ppm |
WaterSolubility |
Solutum in aqua Aether alcohols, benzene, acetone, Chloroform. |
sensitivo |
lux sensitiva |
Number JECFA |
1304 |
Merck Poland |
14,8560 |
BRN |
111296 |
Stabilitatem: |
Firmum et lucis sensistive. Foetor Repugnat oxidizingagents fortis fortis acida, acidum ahydrides acid Caustic. Combustibilis ab aere obscuritas. |
InChIKey |
ZFRKQXVRDFCRJG UHFFFAOYSA-N, |
CASDataBase Reference |
83-34-1 (CAS DataBase Reference) |
NIST ChemistryReference |
1H, Indole, methyl--III (83-34-1) |
Ratio Subcriptio EPASubstance |
Methylindole-III (83-34-1) |
HazardCodes |
XI, N |
RiskStatements |
XXXVI / XXXVII / 38-51 / LIII |
SafetyStatements |
26-36-61 |
RIDADR |
UN3077 - genus IX - III PG - DOT / IATA UN3335 - environmentally hazardoussubstances, solidae, n.o.s., III: Omnia (non BR) |
Germania WGK |
2 |
RTECS |
NM0350000 |
F |
8-13 |
Capparis |
Ita |
HS Code |
29339920 |
Data HazardousSubstances |
83-34-1 (Malo Periculosam substantias Indicium) |
Aedes |
MLD in sponsione ranarum (mg / kg): M s.c. (Bin-Ichi) |
chemicae |
Est quaedam alba crystal. In 265-266 ° C ferventis punctum est; meltingpoint 93-96 ° C est; solutum in ethanol et oleum XCV% of spices ter itsvolume. Non habet indole, ut fumus aromatum de animalium et terra salsuginis et strongflavor. Sapor praevalens viribus proliferating firma perpetuo et per longum tempus. Facit illud excelsum concentratio tetra modo nimis et bestiae campi magnam gestat sicut civet likeincense. Praeterea, sicut quod est calidum mitia saporem. |
Quod maximum licita vexillum moles et residuum, |
Nomine additives: methyl indole eos dictos isto |
productio methodis |
III, in praesenti Methylindole civet, hominum, caseum, lac, et tea.Propionaldehyde et phenylhydrazine potest removere aqua calefacta ad moleculesto obtain propanal phenylhydrazone in industriae productio, et theintermediates interque fervorem cadmiae chloride aut acidum SULPHURATUS, per removalof ammoniaci spectare possit moleculis III, Methylindole. |
ChemicalProperties |
brunneas platelets |
Properties eget |
Skatole habet de ratione putre corporis nostri tabernaculum ad fecal odor concentratione alto, becoming iucundum, Aenean, ut, fruity dulcis, calidum lowconcentrations ad ipsum. Hoc est calidum overripe fruity saporem infra I ppm. |
usibus |
Lepidissima fluorescent guanosine analogon, et per dimethoxytrityl, phosphoramidite protected forma, inserta esse situm, in specie per III intooligonucleotides? V? Phosphodiester in nexu usura automated DNAsynthesizer |
usibus |
animal attractant |
usibus |
A natura pneumotoxin abundat, praesertim in animantibus invenimus fecesproviding fortes ejus fecal odor. Concentratione in inferioribus tamen habet thecompound placebit odoris et flores aurei dans la smine theirpleasing odore vestigans. Est saepe est pars commercial andperfumes suavitatis suæ. |
definitio |
ChEBI: A 3. statum methylindole portantem promovit ad yl substituent isproduced est Dominus in anoxic metabolismi de tryptophan in mammaliandigestive tractus. |
Aroma limine values |
DEPREHENSIO: 0,2 bilionem |
salutem Profile |
Venenum per ingestion, intravenous et intraperitoneal partibus. Moderatelytoxic telae in itinere. Corrumpi autem succensa emittit toxicfumes Nox. |
Synthesis eget |
Indoles (skatole) with II et III variis substituents in synthesim redigentes situ sciri per Fissher in summa indole, consistit in duobus gradibus andutilizes aliphaticorum et aromaticorum phenylhydrazine et aldehyde ketone asstarting seu materiae. |
metabolicae Tractus |
Tres major tenuissimum, skatole 14C-sunt in plasma / ofpigs urina sunt, et dedit skatole identified as-VI sulfatoxyskatole,-III-III-hydroxy methyloxindole et mercapturate adduct de skatole, III - [(N-acetylcysteine-S- y ') yl] indole. Nam alias vias, videatur thereferences in textu. |
et rudis materiae |
Indazole-III-acid -> fetus -> phenylhydrazone -> Kyvet |