HS Code Lookup for Heading 2925
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WCO Notes for Heading 2925
29.25 - Carboxyimide-function compounds (including saccharin and its salts) and imine-function compounds.
- Imides and their derivatives; salts thereof :
2925.11 - - Saccharin and its salts
2925.12 - - Glutethimide (INN)
2925.19 - - Other
- Imines and their derivatives; salts thereof :
2925.21 - - Chlordimeform (ISO)
2925.29 - - Other
(A) IMIDES
Imideshave the general formula (R=NH), where R is a dibasic acyl radical.
(1) Saccharin or 1,2-benzisothiazolin-3-one 1,1-dioxide and its salts*. Saccharin is an odourless, white crystalline powder having a very sweet taste; its sodium and ammonium salts have a lower sweetening power but are more soluble. Tablets consisting solely of one of these products remain in this heading.
Preparations, used in human diets, consisting of a mixture of saccharin or its salts and a foodstuff, such as lactose, are however excluded from this heading and fall in heading 21.06 (see Note 1 (b) to Chapter 38). Those preparations consisting of saccharin or its salts and substances, other than a foodstuff, such as sodium hydrogencarbonate (sodium bicarbonate) and tartaric acid fall in heading 38.24.
(2) Succinimide, used in chemical synthesis.
(3) Phthalimide, used in chemical synthesis.
(4) Glutethimide. A psychotropic substance - see the list at the end of Chapter 29.
Organic imide derivatives of inorganic acids are classified in heading 29.29.
(B) IMINES
Imines, like imides, are characterised by the group =NH, but it is linked to a non-acidic organic radical : (R2C=NH).
(1) Guanidines*. The action of cyanamide on ammonia gives an imino-urea known as guanidine; this can be regarded as derived from urea by replacing the oxygen of the (
C=O) group by an imino group (=NH) :
H2NCONH2...................................................................... (H2N)2C=NH
urea guanidine
Guanidine is also formed in the oxidation of proteins; it can also be obtained synthetically. It is crystalline, colourless and deliquescent.
Its derivatives include :
(a) Diphenylguanidine*. Rubber accelerator.
(b) Di-o-tolylguanidine. Rubber accelerator.
(c) o-Tolyldiguanide. Rubber accelerator.
(2) Aldimines. These have the general formula (RCH=NR1) where R and R1are alkyl or aryl radicals (methyl, ethyl, phenyl, etc.) or sometimes hydrogen.
They constitute the products known as Schiff’s bases, the most important of which are :
(a) Ethylideneaniline.
(b) Butylideneaniline.
(c) Aldol-a- and -b-naphthylamines.
(d) Ethylidene-p-toluidine.
All these products are used in the rubber industry.
(3) Imino ethers*.
(4) Amidines.
(5) 2,6-Dichlorophenolindophenol.
This heading excludes, however, cyclic polymers of aldimines (heading 29.33).
