Isoamyl Butyrate
  • Isoamyl ButyrateIsoamyl Butyrate

Isoamyl Butyrate

Isoamylbutyrats cas-kode er 106-27-4

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produktbeskrivelse

Isoamyl butyrate Basic information


Description References


Produktnavn:

Isoamyl butyrate

CAS:

106-27-4

MF:

C9H18O2

MW:

158.24

EINECS:

203-380-8

Mol-fil:

106-27-4.mol



Isoamylbutyrat Kjemiske egenskaper


Smeltepunkt

-73 °C

Boiling point 

184-185 °C(lit.)

tetthet

0,862 g / ml ved 25 ° C (opplyst)

damptetthet

5.45 (mot luft)

damptrykk

1.1 hPa (20 °C)

refractive index 

n20/D 1.411(lit.)

FEMA 

2060 | ISOAMYL-BUTYRAT

Fp

136 °F

storage temp. 

Oppbevares under + 30 ° C.

løselighet

0,5 g / l

form 

neat

Specific Gravity

0.866 (20/4℃)

Merck

14,5115

JECFA-nummer

45

InChIKey

PQLMXFQTAMDXIZ-UHFFFAOYSA-N

CAS DataBase Reference

106-27-4(CAS DataBase Reference)

NIST Chemistry Reference

Butansyre, 3-metylbutylester (106-27-4)

EPA Substance Registry System

Isoamylbutyrat (106-27-4)


Isoamyl butyrate Safety Information


Hazard Codes 

Xi

Risk Statements 

36/37/38

Safety Statements 

26-36 / 37 / 39-24 / 25

RIDADR 

UN 3272 3/PG 3

WGK Tyskland

1

RTECS

ET5034000

TSCA

Ja

HazardClass

3

PackingGroup 

III

HS kode

29156019

Toxicity

LD50 oralt i kanin:> 5000 mg / kg LD50 hud Kanin> 5000 mg / kg


Isoamyl butyrate Usage And Synthesis


Beskrivelse

Isoamyl Butyrate is a chemical ester of butyrate. It is a kind of flavoring agent that widely used in the preparation of a variety of fruit juice flavor, such as apricots, bananas, pears, apples and other flavor. It is high-demand flavor and fragrance compounds widely used in the food, beverage, cosmetic, and pharmaceutical industries. It is also a kind of solvent for extracting natural spices and the solvent of acetate fiber. Its synthesis can be mediated by the lipase (from various sources) catalyzed esterfication of isoamyl alcohol and butyrate.

References

Macedo, G. A., G. M. Pastore, and M. I. Rodrigues. "Optimising the synthesis of isoamyl butyrate using Rhizopus sp. lipase with a central composite rotatable design." Process Biochemistry 39.6 (2004): 687-693.
Krishna, S. Hari, et al. "Lipase-catalyzed synthesis of isoamyl butyrate: optimization by response surface methodology." Journal of the American Oil Chemists' Society 76.12 (1999): 1483- 1488.
Langrand, G., C. Triantaphylides, and J. Baratti. "Lipase catalyzed formation of flavour esters." Biotechnology Letters 10.8 (1988): 549-554.

Beskrivelse

Isoamyl butyrate has a strong, characteristic, fruity (pear-like) odor and a sweet, corresponding taste. Usually prepared by esterification of commercial isoamyl alcohols with butyric acid by heating in the presence of TwitchelFs reagent; or by fermentation from butyric acid and isoamyl alcohol.

Chemical Properties

Isoamylbutyrat har fruktig, aprikos, ananas, banan, sterk, karakteristisk lukt og asweet, tilsvarende smak

Chemical Properties

Isoamyl Butyrate is a liquid with strongly fruity odor that occurs, for example, in banana. It is used mainly in fruit flavors.

Chemical Properties

Klar fargeløs flytende

Uses

manufacture of artficial rum and fruit essences.

Uses

Isoamyl Butyrate is a synthetic flavoring agent that is a stable, col- orless liquid of strong fruity odor. it is usually prepared by esterifica- tion of isoamyl alcohols with butyric acid. it is soluble in most fixed oils and mineral oil and is insoluble in glycerin and propylene gly- col. storage should be in glass, tin, or resin-lined containers. it is used in fruit flavors such as pineapple, raspberry, and strawberry and has application in dessert gels, puddings, and baked goods at 50–60 ppm.

Definition

ChEBI: The butanoate ester of isoamylol.

Preparation

Vanligvis tilberedt ved forestring av kommersielle isoamylalkoholer med smørsyre ved oppvarming i nærvær av Twitchells reagens; eller ved gjæring fra smørsyre og isoamylalkohol

Taste threshold values

Smakskarakteristikker ved 10 spm: moden fruktig, fet, banan, eple, melon og gjæret whisky


Isoamyl butyrate Preparation Products And Raw materials


Råvarer

Kalsiumklorid -> 3-metyl-1-butanol -> (3R, 4S) -1-benzoyl-3- (1-metoksy-1-metyletoksy) -4-fenyl-2-azetidinon -> Tungstinsyre


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