Home | Introduction | Site Map | Success Stories | Research | Products | FAQ | Contact Us | WWC Audio |

 

 • Introduction
 •
Important Warning  
 •
About Vitamin B17
 •
Vitamin B17 as Preventative
 •
Metabolic Therapy in Cancer
 • B17 In Metabolic Therapy
 •
Laetrile and Cyanide
 •
Graphic on Action of B17
 •
Frequently Asked Questions
 •
B17 Therapy Components
 •
Accessory Supplements
 •
B17 Therapy Overview
 •
Therapies and Protocols
 •
What is in B17 Therapy?
 •
Maintenance Dosages
 •
Accessory Therapies
 •
Positive Thinking
 •
Implementing Changes
 •
Behaviour of Tumours
 •
Criteria For Evaluation
 •
B17 - Sickle Cell Anaemia
 •
Fluoridation-linked cancer
 •
Contacts 
 •
In God We Trust
 •
References

•  More Studies, Research

 

 

 

 

 

 

 

 


 

 

 

 

 

 

 

 

 

 

 

 

 

 

CHAPTER IV

PHYSICAL AND CHEMICAL CHARACTERISTICS
 


Physical and Chemical Characteristics

AMYGDALIN, a vegetable extracted from the nut of the apricot by the method described in the previous section, is a crystalline powder with the following characteristics:

1. Chemical Name.

D-rnandelonitrile-beta-gIucoside-6-beta-D-gIucoside

2. Structural Formula.

 

3. Condensed Formula.

4. Molecular Weight.

457.42 in anhydrous base.

5. Description.

White, crystalline, inodorous powder with a pronounced bitter taste.

6. Solubility.

Slightly soluble in cold water, alcohol, and acetone. Very soluble in hot water, alcohol, and acetone. Insoluble in either.

 

Methods of Identification

A. A 0.1% solution of AMYGDALIN in distilled water, shows on the ultraviolet light spectrum, a maximum absorption of 268, 262, and 257 microns and a minimum absorption between 250 and 253 microns of wave length.

B. A 1 % solution of AMYGDALIN hydrolyzed by reflux with five ml of concentrated hydrochloric acid per 100ml of solution, for one hour, gives the following positive reactions:

BENZALDEHYDE: To five ml of the hydrolyzed solution is added two ml of 10% sodium hydroxide. Upon heating, there appears a strong odor of almond which increases upon boiling.
HYDROCHLORIC ACID:
To five ml of the hydrolyzed solution is added one ml of recently prepared 10% ferrous sulphate, two ml of 10% sodium hydroxide, one ml of 10% ferric chloride and three ml of hydrochloric acid; heat slowly until boiling and a blue color appears and a precipitate of the same color a few minutes later.
REDUCING SUGARS: To five ml of the hydrolyzed solution is added two ml of alkaline solution of cupric tartrate (S.R.) and is heated to boiling: Almost at once there appears an abundance of brick colored precipitate.

Tests for Purity

A.
 
Point of fusion.
Trihydrated AMYGDALIN has its point of fusion between 210° and 218° C.
B.
 
Loss during drying.
Not greater than 12% after being exposed to 105° C for two hours.
C.
 
Residue upon ignition.
Not greater than 0.2% after exposure to 600°C for three hours.
D.
 
Clarity and color of the solution.
The solution of 1% AMYGDALIN in distilled water is clear and colorless.
E.
Specific rotation.
A 5% solution of AMYGDALIN in distilled water is levorotatory (or negative) between -37° and 42°.
F.

 

Absence of free cyanide.
After dissolving 200 mg of AMYGDALIN in five ml of double distilled water, add to it one ml of 10% recently prepared ferrous sulphate, two ml of 10% sodium hydroxide, one ml of 10% ferric chloride and three ml of diluted hydrochloric acid. When heated to the boiling point neither blue color nor blue precipitate appears.
G.
 
Absence of reducing sugars.
If one ml of alkaline cupric sulphate is added to a 5% solution of AMYGDALIN and brought to a boil, the characteristic brick colored precipitate does not appear.


 

 

2001 Worldwithoutcancer.org.uk
By Accessing this web site you accept  all its terms and conditions.

©Copyright 2000 - Worldwithoutcancer.org.uk - PO Box 2038 - Leigh-on-Sea - SS9 2ZB - UK
Home | Introduction | Site Map | Success Stories | Research | Products | FAQ | Contact Us | WWC Audio |