Ketones; acyclic, without other oxygen function, 4-methylpentan-2-one (methyl isobutyl ketone)
HS v2017 Code: 291413
About ketones; acyclic, without other oxygen function, 4-methylpentan-2-one (methyl isobutyl ketone)
HS code 291413 covers the classification of 4-methylpentan-2-one, also known as methyl isobutyl ketone (MIBK). This organic compound is an important industrial solvent and chemical intermediate used in a wide range of applications across various industries. As an acyclic ketone, MIBK plays a crucial role in the production of paints, coatings, adhesives, and other chemical formulations, making it a vital component in the global manufacturing landscape.
Production process
The primary production method for MIBK involves the catalytic hydrogenation of acetone, a process that converts the raw material into the desired ketone. This reaction is typically carried out under controlled temperature and pressure conditions, often with the aid of metal catalysts to improve efficiency and yield. The resulting MIBK is then purified and refined to meet the specific quality and purity requirements of its intended applications.
Production inputs
The main inputs required for the production of MIBK include acetone as the primary raw material, as well as hydrogen gas, catalysts, and various processing equipment such as reactors, distillation columns, and storage tanks. The availability and cost of these inputs can significantly impact the overall production and supply of MIBK in the global market.
Production outputs
The primary output of HS code 291413 is 4-methylpentan-2-one, or methyl isobutyl ketone (MIBK). This versatile chemical is widely used as a solvent in the production of 321110 Paints and varnishes, 350610 Adhesives, and various other chemical formulations. MIBK may also be further processed or combined with other substances to create a range of downstream products classified under different HS codes, such as 290590 Other acyclic alcohols and 291429 Ketones, cyclic, without other oxygen function, n.e.c. in heading 2914.
Revisions to 291413
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 291413. The most recent 1 version of this code (291413) is in the HS v2022 system:
This page shows a legacy version of code 291413 ( HS v2017).
Newer versions
- HS v2022 (Latest revision):
Older versions
Family tree for ketones; acyclic, without other oxygen function, 4-methylpentan-2-one (methyl isobutyl ketone)
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/v2017/291413'>291413: Ketones; acyclic, without other oxygen function, 4-methylpentan-2-one (methyl isobutyl ketone)</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/v2017/291419'>291419: Ketones; acyclic, without other oxygen function, n.e.c. in item no. 2914.1</a>"] B --> G["<a href='/classifications/hs/v2017/291422'>291422: Ketones; cyclanic, cyclenic or cycloterpenic, without other oxygen function, cyclohexanone and methylcyclohexanones</a>"] B --> H["<a href='/classifications/hs/v2017/291423'>291423: Ketones; cyclanic, cyclenic or cycloterpenic, without other oxygen function, ionones and methylionones</a>"] B --> I["<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 --> J["<a href='/classifications/hs/v2017/291431'>291431: Ketones; aromatic, (without other oxygen function), phenylacetone (phenylpropan-2-one)</a>"] B --> K["<a href='/classifications/hs/v2017/291439'>291439: Ketones; aromatic, (without other oxygen function), excluding phenylacetone (phenylpropan-2-one)</a>"] B --> L["<a href='/classifications/hs/v2017/291440'>291440: Ketone-alcohols and ketone-aldehydes</a>"] B --> M["<a href='/classifications/hs/v2017/291450'>291450: Ketone-phenols and ketones with other oxygen function</a>"] B --> N["<a href='/classifications/hs/v2017/291461'>291461: Quinones; anthraquinone</a>"] B --> O["<a href='/classifications/hs/v2017/291462'>291462: Quinones; coenzyme Q10 (ubidecarenone (INN))</a>"] B --> P["<a href='/classifications/hs/v2017/291469'>291469: Quinones; other than anthraquinone and coenzyme Q10 (ubidecarenone (INN))</a>"] B --> Q["<a href='/classifications/hs/v2017/291471'>291471: Ketones and quinones; halogenated, sulphonated, nitrated or nitrosated derivatives; chlordecone (ISO)</a>"] B --> R["<a href='/classifications/hs/v2017/291479'>291479: Ketones and quinones; halogenated, sulphonated, nitrated or nitrosated derivatives, other than chlordecone (ISO)</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 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 %% class C highlight