Ketones and quinones; halogenated, sulphonated, nitrated or nitrosated derivatives, other than chlordecone (ISO)

HS v2017 Code: 291479

About ketones and quinones; halogenated, sulphonated, nitrated or nitrosated derivatives, other than chlordecone (iso)

HS code 291479 covers a diverse range of chemical compounds known as ketones and quinones, along with their halogenated, sulphonated, nitrated, or nitrosated derivatives. These compounds play a crucial role in various industries, from pharmaceuticals and agrochemicals to specialty chemicals and materials. Their versatility and unique properties make them indispensable in the production of a wide array of consumer and industrial products, contributing significantly to the global economy.

Production process

The production of the chemicals covered under HS code 291479 typically involves a range of chemical synthesis techniques, such as oxidation, reduction, and substitution reactions. These processes are often carried out in controlled environments, utilizing specialized equipment and carefully monitored reaction conditions to ensure the desired product quality and purity.

Production inputs

The main inputs required for the production of the chemicals under HS code 291479 include a variety of raw materials, such as organic compounds, halogens, sulfur-containing compounds, and nitrating or nitrosating agents. Additionally, the industry relies on specialized equipment, including reactors, distillation columns, and purification systems, as well as skilled labor and technical expertise to manage the complex chemical processes involved.

Production outputs

The chemicals produced under HS code 291479 find applications in a wide range of industries, including 300000 Pharmaceutical products, 380000 Chemical products, and 390000 Plastics and articles thereof. These compounds are used as intermediates, solvents, and functional additives in the manufacture of a diverse array of products, from pharmaceuticals and agrochemicals to specialty coatings and materials.

Revisions to 291479

Classification codes are adjusted frequently. The code may have been revised or replaced between system versions. The table below shows the history (newest to oldest) of the code 291479. The most recent 1 version of this code (291479) is in the HS v2022 system:

This page shows a legacy version of code 291479 ( HS v2017).

Family tree for ketones and quinones; halogenated, sulphonated, nitrated or nitrosated derivatives, other than chlordecone (iso)

    graph LR
    A["<a href='/classifications/hs/v2017/29'>29: Organic chemicals</a>"]
A --> B["<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>"]
B --> C["<a href='/classifications/hs/v2017/291479'>291479: Ketones and quinones; halogenated, sulphonated, nitrated or nitrosated derivatives, other than chlordecone (ISO)</a>"]

    B --> D["<a href='/classifications/hs/v2017/291411'>291411: Ketones; acyclic, without other oxygen function, acetone</a>"]
B --> E["<a href='/classifications/hs/v2017/291412'>291412: Ketones; acyclic, without other oxygen function, butanone (methyl ethyl ketone)</a>"]
B --> F["<a href='/classifications/hs/v2017/291413'>291413: Ketones; acyclic, without other oxygen function, 4-methylpentan-2-one (methyl isobutyl ketone)</a>"]
B --> G["<a href='/classifications/hs/v2017/291419'>291419: Ketones; acyclic, without other oxygen function, n.e.c. in item no. 2914.1</a>"]
B --> H["<a href='/classifications/hs/v2017/291422'>291422: Ketones; cyclanic, cyclenic or cycloterpenic, without other oxygen function, cyclohexanone and methylcyclohexanones</a>"]
B --> I["<a href='/classifications/hs/v2017/291423'>291423: Ketones; cyclanic, cyclenic or cycloterpenic, without other oxygen function, ionones and methylionones</a>"]
B --> J["<a href='/classifications/hs/v2017/291429'>291429: Ketones; cyclanic, cyclenic or cycloterpenic, without other oxygen function, other than cyclohexanone, methylcyclohexanones, ionones, and methylionones</a>"]
B --> K["<a href='/classifications/hs/v2017/291431'>291431: Ketones; aromatic, (without other oxygen function), phenylacetone (phenylpropan-2-one)</a>"]
B --> L["<a href='/classifications/hs/v2017/291439'>291439: Ketones; aromatic, (without other oxygen function), excluding phenylacetone (phenylpropan-2-one)</a>"]
B --> M["<a href='/classifications/hs/v2017/291440'>291440: Ketone-alcohols and ketone-aldehydes</a>"]
B --> N["<a href='/classifications/hs/v2017/291450'>291450: Ketone-phenols and ketones with other oxygen function</a>"]
B --> O["<a href='/classifications/hs/v2017/291461'>291461: Quinones; anthraquinone</a>"]
B --> P["<a href='/classifications/hs/v2017/291462'>291462: Quinones; coenzyme Q10 (ubidecarenone (INN))</a>"]
B --> Q["<a href='/classifications/hs/v2017/291469'>291469: Quinones; other than anthraquinone and coenzyme Q10 (ubidecarenone (INN))</a>"]
B --> R["<a href='/classifications/hs/v2017/291471'>291471: Ketones and quinones; halogenated, sulphonated, nitrated or nitrosated derivatives; chlordecone (ISO)</a>"]

    

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    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



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class B level4
class C level6
class D level6
class E level6
class F level6
class G level6
class H level6
class I level6
class J level6
class K level6
class L level6
class M level6
class N level6
class O level6
class P level6
class Q level6
class R level6

  class C highlight

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  %% class J,K,L,M,N,O,P level3
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