Page 9 - Phytochemistry 2 (06-PG 605)

2-The substituents and functional groups adjacent to the N. atoms.
 The presence of electron withdrawing groups adjacent to N-atom will
decrease basicity of alkaloids e.g. (Cl, I, Br, O, C=O)

Weakly basic alkaloids form salts only with strong acids and easily hydrolysed with
water, e.g. purine bases

Neutral alkaloids, e.g. ricinine and colchicine can not form salts with acids.

On the other hand,

 The presence of electron donating grps (alkyl groups) adjacent to N-
atom this will increase basicity of alkaloids e.g. coniine.

• Alkaloidal bases acid Alkaloidal salts

• Alkaloidal salts alkali Alkaloidal bases

 The majority of alkaloids (pH 4.5 - 8) are alkaline to litmus paper and methyl
red (pH 4-6) but neutral to Ph. Ph. (pH 8.3-10).

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