III, Methylindole
  • III, MethylindoleIII, Methylindole

III, Methylindole

III-codice est 83-34-1 Methylindole scriptor syndrome

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III, Methylindole Basic notitia


Vexillum uses the eget proprietatibus maximum licita moles productio modos et residuum,


Product Name:

III, Methylindole

CAS:

83-34-1

MF:

C9H9N

MW:

131.17

EINECS:

201-471-7

Mol File:

83-34-1.mol



Donec III, Methylindole Properties


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)


III, Methylindole Safety Information


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)


Atque Usu III-Methylindole Synthesis


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
Licet cibum ELOGIUM nomine cibus
ELOGIUM ad munus concinnanda: aromata in cibum
Quantum maxime permissam (g / kg) De compositis aromata ut moles essentia putandam maximum licita moles partis inferioris quam per GB, et reliqua pedibus MMDCCLX enumerantur.
Reliqua pedibus maxime permissam (g / kg)

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.


Praeparatio-III Methylindole Rudis materia et Products


et rudis materiae

Indazole-III-acid -> fetus -> phenylhydrazone -> Kyvet


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