Ketones; acyclic, without other oxygen function, n.e.c. in item no. 2914.1

HS v2022 Code: 291419

About ketones; acyclic, without other oxygen function, n.e.c. in item no. 2914.1

HS code 291419 covers a broad range of acyclic ketones, which are organic compounds containing a carbonyl group (C=O) without any other oxygen function. These ketones are widely used in various industries, including solvents, fragrances, and chemical intermediates. They play a crucial role in the production of a diverse array of consumer and industrial products, making them an essential part of the global economy.

Production process

The production of acyclic ketones covered under HS code 291419 typically involves a multi-step process. The primary method is the oxidation of alcohols or the dehydrogenation of secondary alcohols. This can be achieved through various techniques, such as catalytic oxidation, electrochemical oxidation, or the use of oxidizing agents like chromic acid or potassium permanganate. The specific production methods may vary depending on the target ketone and the desired purity levels.

Production inputs

The main inputs required for the production of acyclic ketones under HS code 291419 include alcohols, oxidizing agents, catalysts, and various solvents and reagents. Depending on the specific ketone being produced, the input materials may include primary or secondary alcohols, as well as other organic compounds. Additionally, specialized equipment, such as reactors, distillation columns, and purification systems, are necessary for the efficient and safe production of these chemicals.

Production outputs

The acyclic ketones covered under HS code 291419 are used as solvents, intermediates, and building blocks in the production of a wide range of products. They find applications in the manufacture of pharmaceuticals, cosmetics, fragrances, plastics, and various other industrial and consumer goods. Some of the other HS codes that may consume the output of this industry include 2914 Ketones and quinones, whether or not with other oxygen function, and their halogenated, sulphonated, nitrated or nitrosated derivatives, 2915 Saturated acyclic monocarboxylic acids and their anhydrides, halides, peroxides and peroxyacids; their halogenated, sulphonated, nitrated or nitrosated derivatives, and 2916 Unsaturated acyclic monocarboxylic acids, cyclic monocarboxylic acids, their anhydrides, halides, peroxides and peroxyacids; their halogenated, sulphonated, nitrated or nitrosated derivatives.

Revisions to 291419

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 291419. The most recent 1 version of this code (291419) is in the HS v2022 system (this version):

This page shows the most recent version of code 291419.

Family tree for ketones; acyclic, without other oxygen function, n.e.c. in item no. 2914.1

    graph LR
    A["<a href='/classifications/hs/v2022/29'>29: Organic chemicals</a>"]
A --> B["<a href='/classifications/hs/v2022/2914'>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/v2022/291419'>291419: Ketones; acyclic, without other oxygen function, n.e.c. in item no. 2914.1</a>"]

    B --> D["<a href='/classifications/hs/v2022/291411'>291411: Ketones; acyclic, without other oxygen function, acetone</a>"]
B --> E["<a href='/classifications/hs/v2022/291412'>291412: Ketones; acyclic, without other oxygen function, butanone (methyl ethyl ketone)</a>"]
B --> F["<a href='/classifications/hs/v2022/291413'>291413: Ketones; acyclic, without other oxygen function, 4-methylpentan-2-one (methyl isobutyl ketone)</a>"]
B --> G["<a href='/classifications/hs/v2022/291422'>291422: Ketones; cyclanic, cyclenic or cycloterpenic, without other oxygen function, cyclohexanone and methylcyclohexanones</a>"]
B --> H["<a href='/classifications/hs/v2022/291423'>291423: Ketones; cyclanic, cyclenic or cycloterpenic, without other oxygen function, ionones and methylionones</a>"]
B --> I["<a href='/classifications/hs/v2022/291429'>291429: Ketones; cyclanic, cyclenic or cycloterpenic, without other oxygen function, other than cyclohexanone, methylcyclohexanones, ionones, and methylionones</a>"]
B --> J["<a href='/classifications/hs/v2022/291431'>291431: Ketones; aromatic, (without other oxygen function), phenylacetone (phenylpropan-2-one)</a>"]
B --> K["<a href='/classifications/hs/v2022/291439'>291439: Ketones; aromatic, (without other oxygen function), excluding phenylacetone (phenylpropan-2-one)</a>"]
B --> L["<a href='/classifications/hs/v2022/291440'>291440: Ketone-alcohols and ketone-aldehydes</a>"]
B --> M["<a href='/classifications/hs/v2022/291450'>291450: Ketone-phenols and ketones with other oxygen function</a>"]
B --> N["<a href='/classifications/hs/v2022/291461'>291461: Quinones; anthraquinone</a>"]
B --> O["<a href='/classifications/hs/v2022/291462'>291462: Quinones; coenzyme Q10 (ubidecarenone (INN))</a>"]
B --> P["<a href='/classifications/hs/v2022/291469'>291469: Quinones; other than anthraquinone and coenzyme Q10 (ubidecarenone (INN))</a>"]
B --> Q["<a href='/classifications/hs/v2022/291471'>291471: Ketones and quinones; halogenated, sulphonated, nitrated or nitrosated derivatives; chlordecone (ISO)</a>"]
B --> R["<a href='/classifications/hs/v2022/291479'>291479: Ketones and quinones; halogenated, sulphonated, nitrated or nitrosated derivatives, other than chlordecone (ISO)</a>"]

    

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    classDef highlight color:#000,fill:#fff,stroke:#000,stroke-width:5px



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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

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