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Flavouring Agents SBK
Flavouring Agents SBK
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INDIAN SCHOOL
SALALAH
BONAFIDE
CERTIFICATE
Date:
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ACKNOWLEDGEMENT
I would like to thank Mr. Sunil Garg, our Chemistry teacher, for all
the help and support in completing this project. Without the
encouragement of our principal, Mr. Deepak Patankar, I would not
have been able to complete this project.
I would also like to thank my parents, friends, and all those who were
involved either directly or indirectly in this project.
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CONTENTS
➢ INTRODUCTION
➢ THEORY
➢ EXPERIMENT
➢ OBSERVATION
➢ RESULT
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INTRODUCTION
Flavouring agents or flavourants are substances added to food items to impart a
desirable flavour or alter the preexisting one by modifying the smell and taste
characteristic of the food.
Flavour compounds include non-volatiles like sugars, amino acids, fatty acids,
and organic acids and volatiles like aromatic hydrocarbons, aldehydes, acetals,
ketones, alcohols, esters, and Sulfur compounds.
THEORY
VANILLIN AND ITS EFFECTS
VANNILIN
COMMON NAME: VANILLA
PHYSICAL APPEARANCE:
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CINNAMALDEHYDE AND ITS EFFECTS
CINNAMALDEHYDE
COMMON NAME: CINNAMON
IUPAC NAME: 3-phenylpropan-1-ol
MOLAR MASS: 132.16 g/mol
BOILING POINT: 248 °C / 478.40 °F / 521.15 K
PHYSICAL APPEARANCE:
Cinnamaldehyde exists as yellowish to
greenish-yellow oily liquid with a strong pungent
cinnamon odor. It is normally insoluble in water and
many organic solvents but is miscible with alcohol and
other flavouring oils.
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EXPERIMENT
AIM:
To isolate the most important bioactive compound from Cinnamomum
zeylanicum L. (Lauraceae) bark oil and detect the presence of Cinnamaldehyde
via Tollen's test.
MATERIALS REQUIRED:
C. zeylanicum bark, separating funnel, steam distillation apparatus, distilled
water, and a clean beaker.
CHEMICALS REQUIRED:
CH2C12, anhydrous Na2SO4 and tollens reagent ([Ag (NH 3 ) 2 ] OH).
PROCEDURE:
Fresh bark (1.5 kg) was subjected to steam distillation in a Clevenger- type
apparatus for 8 hours.
The distillate (water plus essential oil) was transferred into a 125-mL separating
funnel. CH2C12 (8 mL) was added to the separating funnel, which was then
capped tightly and shaken vigorously with occasional venting.
Layers were separated, and the lower CH2C12 layer was transferred to a clean
beaker. The extraction process was repeated with two more 8- mL portions of
CH2C12 and all the fractions were collected. The combined CH2C12 layers
were washed with 10-20 mL distilled water and separated into a dry container.
The organic layer was dried with three or four small spatulas of anhydrous
Na2SO4 and allowed to set for 10-15 min with occasional swirling, then rinsed
with CH2C12 which was finally evaporated with gentle heating.
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OBSERVATION
The above organic mixture was then subjected to 2 mL of tollen's reagent [Ag
(NH 3)2] OH in a test tube which was then placed in a water bath set at 35°C
for 5 min. A silver mirror resulted around the test tube, which confirms that the
RESULT
PHENYL PROPANOIC
CINNAMALDEHYDE
ACID
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BIBLIOGRAPHY
THEORY: https://en.wikipedia.org
EXPERIMENT: https://www.tandfonline.com/doi/full/10.1080/13880200802430607