3-Methylindole
  • 3-Methylindole 3-Methylindole

3-Methylindole

III-Methylindole cas code est 83-34-1

Model:83-34-1

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III-Methylindole Basic informationes


Chemical proprietatibus Utitur mensura licita maximam quantitatem et residuas productionis modos


Product nomen:

3-Methylindole

CAS;

83-34-1

MF:

C9H9N

MW:

131.17

EINECS:

201-471-7

Mol fasciculi:

83-34-1.mol



III-Methylindole Chemical Properties


Exustio punctum 

92-97 °C(lit.)

Fervens punctum 

265-266 °C(lit.)

density 

1.0111 (aestima)

FEMA 

3019 | BOXED

refractivus index 

1.6070 (aestima)

Fp 

CXXXII °C

repono temp. 

Repone infra +30°C.

pka

17.30 ± 0.30 (Predicta)

forma 

Crystallina pulveris vel Flakes

color 

Fere alba vel pallide brunnea

Odor

odoris indole, sicut

Odor Limen

0.0000056ppm

Aquae Solubilitas 

Aquae solubiles, Aether, Alcohols, Benzene, Acetone, Chloroformia.

Sensitiva 

lux Sensitiva

JECFA Number

1304

Merck 

14,8560

BRN 

111296

Stabilitas:

Stabilis, sed levis, sensitiva. Stench! Fortis repugnare oxidizing agentia, acida valida, acida ahydrides, chlorides acidorum. Combustible.

InChIKey

ZFRKQXORJGRJGRJGRJGRJGRJGHAYS-N

CAS DataBase Reference

83-34-1 (CAS Reference)

NIST Chemia Reference

1H-Indole, 3-methyl-(83-34-1)

EPA Substantia Subcriptio Ratio

3-Methylindole (83-34-1)


III-Methylindole Salutis Information


Discrimen Codes 

Petere

Risk Dictiones 

36/37/38-51/53

salus Dictiones 

26-36-61

RIDADR 

UN3077 - class 9 - PG 3 - DOT/IATA UN3335 - Environmentaliter ancipitia substantiae solidae n.o.s., HI: all (not BR);

WGK Germania 

2

RTECS 

NM0350000

8-13

TSCA 

Ita

HS Code 

29339920

Ancipitia Datae substantiae

83-34-1 (Ancipitia substantiarum data)

Toxicity

MLD in ranis (mg/kg): 1000 s.c. (Bin-Ichi)


3-Methylindole Ritus et Synthesis


Proprietates chemica

Genus est crystallum album. Ferventio C. 265-266°; liquefactio punctum 93-96° C; solutum in XCV% ethanol praeservatum et oleum aromata ter eius volumen. Habet animalium inertes thymiamatis salso et valido olere. Sapor validissimus est, solido ingenio et multiplicando diuturnus diuturnus. Alta intentione homines abominabiles facit; sed valde humilis intentionem magnam gerit civet sicut et animalia similia incensum. Habet autem saporem fructiferum calidum maturum.

Vexillum de licita maxime quantum et residua

Nomen additivorum: β-methyl indoles
Nomen cibi licita pro additivo: cibus
Munus ELOGIUM: Aromata in cibo
Maxime permissam quantitatem (g/kg): moles aromatum ad essentiam compositis infra quam licita maxima copia et residua in GB 2760 enumerantur.
Maxime licita residua (g/kg)

Modi productione

3-Methylindole in zibete, homine, caseo, lacte et tea adest. Propionaldehyde et phenylhydrazine possunt calefieri ad removendum aquae moleculae propanal phenylhydrazone in productione industriae obtinere, ac deinde intermedia calefacta cum acido chlorido chlorido vel sulphurico, per remotionem ammoniaci moleculae 3-Methylindolae obtinere possunt.

Chemical Properties

leviter brunneis platelets

Chemical Properties

Skatole habet proprium putridum, odoris fecalis in concentrationes; iucundus factus, Aenean similis, fruitus suavis, valde calidus concentrationes. Habet saporem fructuosum calidum overripe infra 1 ppm.

usus

Analogia guanosina valde fluorescens, quae in dimethoxytritylo; phosphoramidite forma conservata, situs speciali modo inseri potest oligonucleotides per III? V? phosphodiester nexu usura an automated DNA synthesizer

usus

insectum attractant

usus

Pneumotoxin naturaliter abundans, praesertim in faecibus mammalium inventa fortem fecal odorem praebens. In inferioribus autem concentratione Compositum odorem suavitatis habet, dans flores aurei, et ja- smina eorum suavem odorem. Componentia saepe est odorum commercii et unguentis.

Definition

ChEBI: A methylindole yl ferens substituens in loco 3. Est produci per anoxic metabolismi Dominus tryptophan in mammalian digestivorum tractus.

Aroma limina values

Deprehensio: 0.2 ppb

salus Profile

Venenum per ingestionem, itinera intravenosa et intraperitonealia. mediocriter telae toxicus ab itinere. Cum calefacta compositione emittit toxicum nidore NOx.

Synthesis chemica

Indoles (skatole) cum variis substitutis in 2 et 3 positio can summatim perstringitur per Synthesin indolem Piscatoris, quae duos gradus implicat ac utitur phenylhydrazine et aliphatico vel aromatico aldehyde vel ketone ut initium materiae.

Semita metabolicae

Tres metabolitae maiores 14C-skatolae inveniuntur in plasmate/urine of porci skatoles dati et identificantur ut 6-sulfatoxyskatole, 3-hydroxy-3-. methyloxindole et mercapturate skatole; 3-[(N-acetylcysteine-S-yl)methyl]indole. For other meatus, see the references in the text.


III-Methylindole Praeparatio Products et Rudis materiae


Rudis materiae

Indazole-3-acidum carboxylicum-->LACTE-->phenylhydrazone-->CIVET


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