|
Product Name: |
ethyl isovalerate |
|
CAS: |
108-64-5 |
|
MF: |
C7H14O2 |
|
MW: |
130.18 |
|
EINECS: |
203-602-3 |
|
Mol File: |
108-64-5.mol |
|
|
|
|
Liquescens punctum |
-99 ° F |
|
Ferveret |
131-133 ° C (Litt.) |
|
density |
0.864 g / ml at25 ° C (Litt.) |
|
vapor pressura |
7.5 mm Aggaei (XX ° C) |
|
refractivam index |
n20 / D 1.396 (lit.) |
|
potenti |
MMCDLXIII | ETHYL ISOVALERATE |
|
Fp |
LXXX ° F |
|
temp repono. |
regio Flammables |
|
solubility |
2.00g / l |
|
forma |
Liquid |
|
color |
Ut patet hyalinae paleyellow |
|
Odor Limen |
0.000013ppm |
|
Merck Poland |
14,3816 |
|
Number JECFA |
196 |
|
BRN |
1744677 |
|
CAS DataBase Reference |
108-64-5 (CAS DataBase Reference) |
|
Quaestiones NIST Reference |
Butanoic acidum: III-methyl-, ethylester (108-64-5) |
|
Ratio Subcriptio quod substantia EPA |
Ethylisovalerate (108-64-5) |
|
risk Denunciationes |
10 |
|
Denunciationes salutem |
16 |
|
RIDADR |
III IR MMMCCLXXII / PG III |
|
Germania WGK |
2 |
|
RTECS |
NY1504000 |
|
F |
13 |
|
Capparis |
Ita |
|
HazardClass |
3 |
|
PackingGroup |
III |
|
HS Code |
29156000 |
|
Description |
Ethyl isovalerate isthe ethyl Esther forma isovalerate formatae inter acidum withisovaleric ethyl arcu. Acidum de Valerio a uirtute probus est, maxime in fructibus (Maior pars unus de Bilberry). Fruity agens naturale quoddam genus foodflavoring sapore odore. Hoc est late usus inperfumery et investigabiles. Hoc est saepe modo summatim perstringitur usingsurfactant iactaret lipase (variis species ab origins) immobilitari magneticnanoparticles. |
|
Properties eget |
sine colore flavo liquido patet topale |
|
Properties eget |
Is autem fruity Isovalerate ethyl hyalinae fluidi odor simile vaccinia. Occursin si fructus, holera et bibitor potiones. Factum est fructus usus est in aromacompositions. |
|
Properties eget |
Ethyl isovaleratehas fortis fruity, vini, sicut odor malus ad Dil. |
|
usibus |
Vocatus potiones solutionfor CONDITIO in CUPPEDIAE. |
|
productio modos |
Ethyl isovalerate isproduced componi acido isovaleric ethanol post Pascha apud ofconcentrated sulphurea bydistillation hydrochloric acidum aut acidum. |
|
productio modos |
Ethyl isovalerate isproduced componi acido isovaleric ethanol post Pascha apud ofconcentrated sulphurea bydistillation hydrochloric acidum aut acidum. |
|
Praeparatio |
Per esterification ofisovaleric Acidum cum ethyl arcu coram H2SO4 intenta. |
|
Aroma limine values |
DEPREHENSIO: 0.01 to0.4 bilionem |
|
Saporem limine values |
Tastecharacteristics ad XXX ppm, fruity, suavis, et baca estry, et quasi maturam, fruity adesse pulposam illam simpliciter. |
|
Communia |
A simili colore oilyliquid forti odore pomorum. Rarior aqua. Vaporsheavier quam aerem. LXXVII mico punctum F. Cutis irritationem clementer videretur. |
|
Agrippina Minor aqua Aeris & |
Flammable.Slightly altus aqua solutum. |
|
Reactividad Profile |
Esther ETHYL ISOVALERATE ambiendis aruis. Tu, ad liberandum acida et esters reflecti ad alcohols andacids per calorem. Fortis et strenuus faciam oxidizing acida potest esse reactionem reactionem ad nos incipientium issufficiently exothermic products. Calor est, idque adurentibus alsogenerated per conuersationem esters solutions. Flammablehydrogen est generari ex metallis et alcali et esters hydrides. |
|
salutem DISCRIMEN |
Inspiratione orcontact ad materiam, ut urere et irritare cute, et oculis meis. Produceirritating ut ignis, aspersos maculis et / vel toxicus vapores. Vapores pellentes, ut vertigine orsuffocation. Liquidum ignis dominandi causam coinquinationis Runoff aqua. |
|
carcinogenicity |
Non enumerantur a ACGIH, California propositionem LXV, IARC, NTP aut OSHA. |
|
Ratio purificatione |
Esther withaqueous lava in V% Na2CO3 ergo aquae CaCl2 abundantia saturantur. CaSO4 anddistil super excoquatur. [Beilstein II II 898] |
|
et rudis materiae |
Etanol -> Isobutyronitrile -> Isovaleric Acidum |
