Organo-sulphur compounds

HS v2017 Code: 2930

Chapter	Heading	Sub-heading
29	30	n/a

Code	2930
Version	HS v2017
Hierarchy Level	4
Datasource	WCO
Chapter	29

Ancestor Codes: Organic chemicals

This Code: Organo-sulphur compounds

Child Codes: Organo-sulphur compounds; thiuram mono-, di- or tetrasulphides; Organo-sulphur compounds; aldicarb (ISO), captafol (ISO) and methamidophos (ISO); Organo-sulphur compounds; 2-(N,N-Diethylamino)ethanethiol; Organo-sulphur compounds; methionine; Organo-sulphur compounds; n.e.c. in heading no. 2930; Organo-sulphur compounds; thiocarbamates and dithiocarbamates; Organo-sulphur compounds; bis(2-hydroxyethyl)sulfide (thiodiglycol (INN))

Sibling Codes (Nearest 5): Diazo-, azo- or azoxy-compounds; Organic derivatives of hydrazine or of hydroxylamine; Nitrogen-function compounds, n.e.c. in chapter 29; Other organo-inorganic compounds; Heterocyclic compounds with oxygen hetero-atom(s) only

About organo-sulphur compounds

HS code 2930 covers a diverse range of organo-sulphur compounds, which are essential in various industries, including pharmaceuticals, agrochemicals, and specialty chemicals. These compounds play a crucial role in the global economy, providing key building blocks for a wide array of products that cater to human needs and drive technological advancements.

Production process

The production of organo-sulphur compounds typically involves a series of chemical reactions, often starting with the introduction of a sulphur-containing functional group to an organic molecule. Common techniques include nucleophilic substitution, electrophilic addition, and oxidation-reduction reactions. Manufacturers employ a range of equipment, such as reactors, distillation columns, and purification systems, to ensure the efficient and precise synthesis of these specialized compounds.

Production inputs

The main inputs required for the production of organo-sulphur compounds include various organic precursors, such as alcohols, aldehydes, and aromatic compounds, as well as inorganic sulphur-containing reagents. Additionally, manufacturers rely on specialized catalysts, solvents, and energy sources to facilitate the necessary chemical transformations. The availability and quality of these raw materials and supporting resources are crucial for the industry's ability to meet the growing demand for these versatile compounds.

Production outputs

Organo-sulphur compounds produced under HS code 2930 find applications in a wide range of industries. They are used as intermediates in the production of 2942 Other organic compounds, 2920 Phosphoric esters and their salts or esters of other inorganic acids, and 2921 Amine-function compounds, among others. These compounds are also directly incorporated into final products, such as pharmaceuticals, pesticides, and specialty chemicals, making them an essential component of the global supply chain.

Family tree for organo-sulphur compounds

    graph LR
    A["<a href='/classifications/hs/v2017/29'>29: Organic chemicals</a>"]
A --> B["<a href='/classifications/hs/v2017/2930'>2930: Organo-sulphur compounds</a>"]

    A --> C["<a href='/classifications/hs/v2017/2901'>2901: Acyclic hydrocarbons</a>"]
A --> D["<a href='/classifications/hs/v2017/2902'>2902: Cyclic hydrocarbons</a>"]
A --> E["<a href='/classifications/hs/v2017/2903'>2903: Halogenated derivatives of hydrocarbons</a>"]
A --> F["<a href='/classifications/hs/v2017/2904'>2904: Sulphonated, nitrated or nitrosated derivatives of hydrocarbons; whether or not halogenated</a>"]
A --> G["<a href='/classifications/hs/v2017/2905'>2905: Acyclic alcohols and their halogenated, sulphonated, nitrated or nitrosated derivatives</a>"]
A --> H["<a href='/classifications/hs/v2017/2906'>2906: Alcohols; cyclic, and their halogenated, sulphonated, nitrated or nitrosated derivatives</a>"]
A --> I["<a href='/classifications/hs/v2017/2907'>2907: Phenols; monophenols, polyphenols, and phenol-alcohols</a>"]
A --> J["<a href='/classifications/hs/v2017/2908'>2908: Phenols or phenol-alcohols; halogenated, sulphonated, nitrated or nitrosated derivatives</a>"]
A --> K["<a href='/classifications/hs/v2017/2909'>2909: Ethers, ether-alcohols, ether-phenols, ether-alcohol-phenols, alcohol peroxides, ether peroxides, ketone peroxides (chemically defined or not); halogenated, sulphonated, nitrated, nitrosated derivative</a>"]
A --> L["<a href='/classifications/hs/v2017/2910'>2910: Epoxides, epoxyalcohols, epoxyphenols and epoxyethers; with a three-membered ring and their halogenated, sulphonated, nitrated or nitrosated derivatives</a>"]
A --> M["<a href='/classifications/hs/v2017/2911'>2911: Acetals and hemiacetals; whether or not with other oxygen function, and their halogenated, sulphonated, nitrated or nitrostated derivatives</a>"]
A --> N["<a href='/classifications/hs/v2017/2912'>2912: Aldehydes, whether or not with other oxygen function; cyclic polymers of aldehydes; paraformaldehyde</a>"]
A --> O["<a href='/classifications/hs/v2017/2913'>2913: Aldehydes; halogenated, sulphonated, nitrated or nitrosated derivatives of products of heading no. 2912</a>"]
A --> P["<a href='/classifications/hs/v2017/2914'>2914: Ketones and quinones; whether or not with other oxygen function, and their halogenated, sulphonated, nitrated or nitrostated derivatives</a>"]
A --> Q["<a href='/classifications/hs/v2017/2915'>2915: Acids; saturated acyclic monocarboxylic acids and their anhydrides, halides, peroxides and peroxyacids; their halogenated, sulphonated, nitrated or nitrosated derivatives</a>"]
A --> R["<a href='/classifications/hs/v2017/2916'>2916: Acids; unsaturated acyclic monocarboxylic, cyclic monocarboxylic, their anhydrides, halides, peroxides and peroxyacids; their halogenated, sulphonated, nitrated or nitrosated derivatives</a>"]
A --> S["<a href='/classifications/hs/v2017/2917'>2917: Acids; polycarboxylic acids, their anhydrides, halides, peroxides and peroxy-acids; their halogenated, sulphonated, nitrated or nitrosated derivatives</a>"]
A --> T["<a href='/classifications/hs/v2017/2918'>2918: Acids; carboxylic acid with additional oxygen function and their anhydrides, halides, peroxides, peroxyacids; their halogenated, sulphonated, nitrated or nitrosated derivatives</a>"]
A --> U["<a href='/classifications/hs/v2017/2919'>2919: Esters; phosphoric, and their salts, including lactophosphates, their halogenated, sulphonated, nitrated or nitrosated derivatives</a>"]
A --> V["<a href='/classifications/hs/v2017/2920'>2920: Esters of other inorganic acids of non-metals (other than of hydrogen halides) and their salts, their halogenated, sulphonated, nitrated or nitrosated derivatives</a>"]
A --> W["<a href='/classifications/hs/v2017/2921'>2921: Amine-function compounds</a>"]
A --> X["<a href='/classifications/hs/v2017/2922'>2922: Oxygen-function amino-compounds</a>"]
A --> Y["<a href='/classifications/hs/v2017/2923'>2923: Quaternary ammonium salts and hydroxides; lecithins and other phosphoaminolipids, whether or not chemically defined</a>"]
A --> Z["<a href='/classifications/hs/v2017/2924'>2924: Carboxyamide-function compounds; amide-function compounds of carbonic acid</a>"]
A --> BA["<a href='/classifications/hs/v2017/2925'>2925: Carboxyimide-function compounds (including saccharin and its salts) and imine-function compounds</a>"]
A --> BB["<a href='/classifications/hs/v2017/2926'>2926: Nitrile-function compounds</a>"]
A --> BC["<a href='/classifications/hs/v2017/2927'>2927: Diazo-, azo- or azoxy-compounds</a>"]
A --> BD["<a href='/classifications/hs/v2017/2928'>2928: Organic derivatives of hydrazine or of hydroxylamine</a>"]
A --> BE["<a href='/classifications/hs/v2017/2929'>2929: Nitrogen-function compounds, n.e.c. in chapter 29</a>"]
A --> BF["<a href='/classifications/hs/v2017/2931'>2931: Other organo-inorganic compounds</a>"]
A --> BG["<a href='/classifications/hs/v2017/2932'>2932: Heterocyclic compounds with oxygen hetero-atom(s) only</a>"]
A --> BH["<a href='/classifications/hs/v2017/2933'>2933: Heterocyclic compounds with nitrogen hetero-atom(s) only</a>"]
A --> BI["<a href='/classifications/hs/v2017/2934'>2934: Nucleic acids and their salts, whether or not chemically defined; other heterocyclic compounds</a>"]
A --> BJ["<a href='/classifications/hs/v2017/2935'>2935: Sulphonamides</a>"]
A --> BK["<a href='/classifications/hs/v2017/2936'>2936: Provitamins, vitamins; natural or reproduced by synthesis (including natural concentrates) derivatives thereof used as vitamins, and intermixtures of the fore-going, whether or not in any solvent</a>"]
A --> BL["<a href='/classifications/hs/v2017/2937'>2937: Hormones, prostaglandins, thromboxanes and leukotrienes, natural or reproduced by synthesis; derivatives and structural analogues thereof, including chain modified polypeptides, used primarily as hormones.</a>"]
A --> BM["<a href='/classifications/hs/v2017/2938'>2938: Glycosides, natural or reproduced by synthesis, and their salts, ethers, esters and other derivatives</a>"]
A --> BN["<a href='/classifications/hs/v2017/2939'>2939: Alkaloids; natural or reproduced by synthesis, and their salts, ethers, esters and other derivatives</a>"]
A --> BO["<a href='/classifications/hs/v2017/2940'>2940: Sugars, chemically pure, other than sucrose, lactose, maltose, glucose and fructose; sugar ethers, sugar acetals and sugar esters, and their salts, other than the products of heading 29.37, 29.38, or 29.39</a>"]
A --> BP["<a href='/classifications/hs/v2017/2941'>2941: Antibiotics</a>"]
A --> BQ["<a href='/classifications/hs/v2017/2942'>2942: Organic compounds; n.e.c. in chapter 29</a>"]

    B --> BR["<a href='/classifications/hs/v2017/293020'>293020: Organo-sulphur compounds; thiocarbamates and dithiocarbamates</a>"]
B --> BS["<a href='/classifications/hs/v2017/293030'>293030: Organo-sulphur compounds; thiuram mono-, di- or tetrasulphides</a>"]
B --> BT["<a href='/classifications/hs/v2017/293040'>293040: Organo-sulphur compounds; methionine</a>"]
B --> BU["<a href='/classifications/hs/v2017/293060'>293060: Organo-sulphur compounds; 2-(N,N-Diethylamino)ethanethiol</a>"]
B --> BV["<a href='/classifications/hs/v2017/293070'>293070: Organo-sulphur compounds; bis(2-hydroxyethyl)sulfide (thiodiglycol (INN))</a>"]
B --> BW["<a href='/classifications/hs/v2017/293080'>293080: Organo-sulphur compounds; aldicarb (ISO), captafol (ISO) and methamidophos (ISO)</a>"]
B --> BX["<a href='/classifications/hs/v2017/293090'>293090: Organo-sulphur compounds; n.e.c. in heading no. 2930</a>"]


    %% Color coordination by level

    classDef level1 color:#000,fill:#a8f9ff,stroke:#333,stroke-width:2px
    classDef level2 color:#000,fill:#e0a458,stroke:#333,stroke-width:1px
    classDef level3 color:#000,fill:#419d78,stroke:#333,stroke-width:1px
    classDef level4 color:#000,fill:#c04abc,stroke:#333,stroke-width:1px
    classDef level5 color:#000,fill:#f1c40f,stroke:#333,stroke-width:1px
    classDef level6 color:#000,fill:#f1c40f,stroke:#333,stroke-width:1px
    classDef highlight color:#000,fill:#fff,stroke:#000,stroke-width:5px



  %% Apply classes
  class A level2
class B level4
class C level4
class D level4
class E level4
class F level4
class G level4
class H level4
class I level4
class J level4
class K level4
class L level4
class M level4
class N level4
class O level4
class P level4
class Q level4
class R level4
class S level4
class T level4
class U level4
class V level4
class W level4
class X level4
class Y level4
class Z level4
class BA level4
class BB level4
class BC level4
class BD level4
class BE level4
class BF level4
class BG level4
class BH level4
class BI level4
class BJ level4
class BK level4
class BL level4
class BM level4
class BN level4
class BO level4
class BP level4
class BQ level4
class BR level6
class BS level6
class BT level6
class BU level6
class BV level6
class BW level6
class BX level6

  class B highlight

  %% class A level1
  %% class B,C level2
  %% class D,E,F,G,H,I level2
  %% class J,K,L,M,N,O,P level3
  %% class B highlight