Skip to main content

Coca-Cola: Life - myth or truth?

"Coca-Cola Life"


Recently the Coca-Cola company released a new beverage: the Coca-Cola Life drink.

It should contain less sugar than the normal Coca-Cola drink; a part of the sugar is replaced with the recently approved sweetener from the Stevia plant (stevioglycosides).

It's being sold as a 'natural' drink, but those stevioglycosides are as natural as the chemical sweetener aspartame found in Light and Zero drinks.

However it is true that the amount of sugar is much lower (being reported as 33%, some say it's around 20%); yet approximately still 3-4 sugar cubes / 33 cl can (5-6 in a normal can).

I bought it myself and found that the flavor has not really changed from the original Coca-Cola, however it does taste more "flat" - but definitely true it yourself.
The outside of the can has the colour green. I personally do not associate this "healthy - natural" colour with Coca-Cola, but it's growing on me.

In summary, it's not a new revolutionary beverage, and mostly is (and maybe will stay) a marketing hype. But the flavour is alright, it's close to Coca-Cola's roots, and most importantly, has effectively less sugar than the original Coca-Cola. Yet keep in mind that if you want to lose weight or reduce your intake of sugar drastically, then do not drink this or the original Coca-Cola, but go for the Light or Zero varieties if you still want to drink this soft drink.


References: media, google, ...



Coca-Cola Company©

Comments

  1. This comment has been removed by a blog administrator.

    ReplyDelete

Post a Comment

Popular posts from this blog

Erythropoietin: definition, structure, synthesis in vivo

Definition: EPO: = erythropoietin   A glycoprotein hormon-like structure, a sialoglycoprotein, which is an important factor in the survival, growth and proliferation of erythroid precursor cells (EPC) and it improves the de novo creation, differentation and growth of red blood cells (RBC). Thus, EPO controls the erythropoiesis = production of RBC. EPC: these are cells that are located in the bone marrow, will eventually form the RBC. RBC: cells responsible for the transport and distribution of oxygen throughout the body. Structure: Built out of 165 aminoacids (AA). They are all connected and form 1 polypeptide chain.  Although, within the chain, there are 2 disulfide bonds.  Respectively on positions: Cys7-161 and Cys29-33  Cys = cystein and the numbers indicate the positions these AA are located. Cystein structure. Available  sulfide  group for bonding There are also 4 positions where there is a possibility for glycosylation  Namel...

Alkylhalides: Substitution reactions 6 (Sn1)

Alkylhalides: Substitution Nucleophile substitution reaction ( Sn1 reaction ) Sn1 side reactions I will now discuss some side reactions that can occur when a Sn1 reaction takes place. Carbocation shift Illustrated in the scheme below: Benzyl- and allylhalides  Benzyl- and allylhalides can undergo Sn1 AND Sn2 reactions. How to distinct them? Sn1 conditions: protic solvent and by adding a weak attacking nucleophile. Note: Benzyl- and allylhalides easily undergo Sn1 reactions, because their carbocations are very stable. Sn2 conditions: aprotic solvent and by adding a strong attacking nucleophile. Note: tertiary benzylhalides and tertiary allylhalides will NOT undergo a Sn2 reaction because of the steric effects (see chapter Sn2 reaction blogposts). Sn2 reaction examples Sn1 reaction examples Sn1 and Sn2 reactions in biology, nature and medicines S-Adenosyl methionine This is a biological methylating agens, also known as SAM . It is a frequen...

Alkanes and radicals 1: Introduction

Alkanes and radicals Introduction Let's start with one of the most complex compounds consisting of alkanes and cycloalkanes (naftenes) that can be separated by distillation: Petroleum . Some tips when writing reactions with radicals, have a look on these reactions below, when an heterolytic bond gets cleaved, the arrowhead gets two barbs. When there is a homolytic bond that gets cleaved the arrowhead that shows the direction of the radical, gets one barb, have a look: Alkanes are little reactive, they will not react fast and heavily, because they only contain strong  sigma  σ bindings (single bonds). They also only have non-partial charged atoms. Although, alkanes DO react with Cl2 and Br2. The reactions are listed below, have a look, first the actual reaction, then shown in detail with different steps :