Sin Isoamyl

Product Name:

Sin Isoamyl

Synonym:

Yl I-III-butano: methylbutan--III, III-methylbutanoI:-III-Metil butanolo: alcool amilico: Alcoolisoamylique: alcoolamilico: alcoolisoamylique

CAS:

123-51-3

MF:

C5H12O

MW:

88.15

EINECS:

204-633-5

Mol File:

123-51-3.mol

Liquescens punctum

-117 ° F

Ferveret

131-132 ° F

density

0,809 g / ml at25 ° C (Litt.)

vapor densitatem,

III (vs caeli)

vapor pressura

II mm Aggaei (XX ° C)

refractivam index

n20 / D 1.407

potenti

MMLVII | ISOAMYL ALCOHOL

Fp

109.4 ° F

temp repono.

regio Flammables

solubility

25g / l

pka

> XIV (Schwarzenbach et al. MCMXCIII)

forma

Liquid

color

Gravitas specifica

0.813 (XV / 4A)

PH

VII (25g / l, H2O, 20a)

Odor

Mitis perdunt suavitatem bibitor, non-residua.

Odor Limen

0.0017ppm

terminus explosive

1.2-9%, 100a ° F

aqua Solubility

XXV g / L (XX ºC)

Î »max

Î »: CCLX Amax m, 0,06
Î »: CCLXXX Amax m, 0,06

Merck Poland

14,5195

Number JECFA

52

BRN

1718835

Henrici de assidua legis

33.1 ° F at XXXVII (Bylaite et al., MMIV)

patefacio fines

REL NIOSH: TWA 100ppm (CCCLX mg / m3): ppm IDLH D; OSHA PEL: ppm TWA C; ACGIH TLV: ppm TWA C, CXXV stel ppm (adopted).

Stabilitatem:

Firmum. Flammable.Incompatible magnis oxidizing agentia fortis acida, acidum chlorides, acidanhydrides.

CAS DataBase Reference

123-51-3 (CAS DataBase Reference)

Quaestiones NIST Reference

I-butanol, methyl--III (123-51-3)

Ratio Subcriptio quod substantia EPA

Methyl-I-III-butanol (123-51-3)

aleam Codes

xII

risk Denunciationes

10-20-37-66-20 / R20-XXII / R10 XXII,

Denunciationes salutem

46-16 S16-

RIDADR

MCV III IR / PG III

Germania WGK

1

RTECS

EL5425000

Autoignition Temperature

DCXLIV ° F

Capparis

Ita

HazardClass

3

PackingGroup

II

HS Code

29335995

Ancipitia substantiae Data

123-51-3 (Malo Periculosam substantias Indicium)

Aedes

LD50 mures inclusi essent in viva voce, 7.07 ml / kg (Smyth)

chemicae

Subhyalina vel pallidus patet flavo oleum liquidum sit. Apple sublimatum CONDITUS odore et sapore. ignis mollibus punctum: -117,2 Â ° C. Ferventis punctum: CXXX Â ° C. Density Relativum (d2525): 0.813. Refractivam index (nD20) 1,4075. Toxicus vapores. Et miscibilia in ethanol praeservatum aether. Solutum in aqua modice.
Naturalis praesentem in forma products in esters nascentia fraga, peppermint, lemongrass, eucalyptus oleum et quod nonnulla in.

Description

Vocatus Isoamyl hasa natura sus et effundens odorem proprium saporem. Industrially paravit ex fusel oleum byrectification.

Properties eget

Vocatus est Isoamyl afusel oleum, cupam, divido, separo sus et effundens odorem proprium saporem.

Properties eget

Amyl alcohols (Pentanols) ut octo isomers. Omnium fomes colore liquido praeter 2,2- isomer in amino-I-propanol, quod est solidum crystallinum.

Properties eget

sine colore humor

Properties eget

I-III-yl odorthreshold quia caeli sicut relata butanol 0.042 ppm, quam acutae providessome correptionem patefacio ut huius eget.

Spermatophyta

Patet, cum a ACUTUS odor colorlessliquid. Odor limine retrahitur a 1.7 ppbv wasreported Yokota et Nagata (MCMXC).

usibus

Methyl-I-II-III-butanoland yl I-sunt butanol Northmanni usus est, sive malum pro CONDITIO agentsfor Musa sapientum fixa est vinum. Et quoque mediate et utendum ut mediis solventibus inpharmaceutical chemical products.

usibus

Unus autem ex pluribus isomers amyl Isoamylol est pelagus ingredient in Vocatus et oleum productionof Musa sapientum fixa.

usibus

Exuberant torcularia quia solvente, dilutum resinam alkaloids, etc .; DOM US vero isoamyl (amyl) Composita, isovaleric acidum, mercurio supernatat fulminare quatinus, pyroxylin, sericum artificialis, lacquers, ACAPNOS pulveris, in Bacteria; Nam dehydrating celloidin solutiones; inmilk adipem ad determinandum.

definitio

ChEBI: An hoc est alkylalcohol I-of-butan substituimus per loco ad yl coetus III.

productio modos

I-III-butanolis usum methyl sicut menstrua pro unguento delibuti, exuberant torcularia: nisl, ac ceris; in plasticsindustry polyacrylonitrile tuant; quam in fabricandis lacquers, chemicals, et in veneficiis. Et usus est pro CONDITIO et infragrances agentibus. Odio enim orci sed principaliter per contactum dermal andinhalation.

Praeparatio

industrially paratus per rectificationem fusel oleum.

Praeparatio

Methyl-I-II-III-butanoland yl I-sunt butanol fusel primos olea solitaria a per-products ofethanol a fermento fermentatio. Compositis his etiam sequitur ex thechlorination pentane hydrolysa est. Alius alternative processis oxo per processum quendam, Afrorum ducem belli exercendis armorum officinis et C4 higheralcohols. Et chlorination et oxo processus productio processus est de processibus ad currentcommercial I-III-yl butanol and2-I-butanol yl, sed per processum et oxo hydroformylation isthe reactionem magis aura popularis ierat. Duo sunt enim technologiae principalis processus. Et intulit firstwas amnis ab Ruhrchemie in Germania Exxon 1940sand est fere in in USA referred to as "summus pressura cobalt catalysttechnology". Activae in catalyst est species hydrocarbonyl cobalt, et apressure 200A de CCC requiratur dolor sit ponere statum thecatalyst. In mane 1960s, Crusta commercialized versio moderna legum thecobalt sedibus processus. Hoc technology usus organophosphine ligands, ad minus operating whichallows 30a pressura C ex actione thecatalyst atm, sed inpensa. In technology crusta est prima alcohols usus praesertim theproduction linearibus, cum autem frequens usus est summus pressura cobalttechnology est productio hyphis ramosis alcohols.

Aroma limine values

DEPREHENSIO: CCL bilionem ppm ad 4,1

Saporem limine values

gustum ppm habet ad L, fusel, fermentato, fruity, Musa sapientum fixa, aetherias Conniaco

Communia

Lexus liquidwith placidam sentire, suffocatio spiritus odoris suavissimi componendum. Rarior aqua solubiles water.Hence aquae supernatet. Asperioribus verbis ipsius fit et vapor.

Agrippina Minor aqua Aeris &

Highly flammable.Water solutum.

Reactividad Profile

-I-III-Methyl butanolattacks materia plastica [Tractantem Albanica sponsorum tutus, 1980, p. CCXXXVI]. Potassium acid fortes faciat explosions.Mixing consectetuer withconcentrated mixta cum sulphurea aqua aquam acido hypochlorous / carbo tetrachloride solutioncan isoamyl Mercury generare, quod praemium praesertim onexposure caloris solis. Cum CHLORUM non miscentes et isoamylhypochlorites cedere [M CDXCI NFPA, MCMXCI]. -Base catalysed reactiones isocyanatescan fieri per violentiam explosive [Wischmeyer, MCMLXIX].

aleam

Modicus ignis periculum. Vapor est toxicus et irritamentum. Explosive in fines caeli 1.2â IX%.

salutem DISCRIMEN

Vaporconcentrations exasperentur oculos altissima tractus respiratorii superioris. Contactwith continua sit causa cutis irritationem.

eget Reactividad

cum Reactividad Aqua, nulla reactionem; Reactividad cum Clementine_Vulgate Materias: nullus motus; Stabilitatem Per Onerariis: Stabull; Acidis propter se curat ut medicamentis agens: Non pertinent; Polimerización: non pertinent; Matrix Polimerización: Non pertinent.

Potentialis expositio

(Isomer-n): Suspecta reprotoxic aleam: Prima irritamentum (v / o allergic reactionem) (iso-, prima): Possibile periculo formatam secretiori parte natium: Prima irritamentum (v / o allergicreaction) (sec-, primary- activae, et alia isomers) prima irritamentum (v / oallergic reactionem). Uti organi nariae syntheticflavoring synthesis, veneficiis, pede inhibitors; Plastics otherchemicals et facere; ut flotation agente. Et (n-isomer) sit usus est in praeparationem oiladditives, plasticizers, synthetica unguenta, sicut et solvent.