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6-Chloro-N-hexanoic acid, also known as 6-chlorocaproic acid, is a synthetic chemical compound that belongs to the class of organic compounds known as medium-chain fatty acids. These fatty acids have a chain length between 4 and 12 carbon atoms. It exhibits moderately acidic properties and is typically found in its solid form. Being industrially synthesized, it is not naturally derived.

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  • 4224-62-8 Structure
  • Basic information

    1. Product Name: 6-CHLORO-N-HEXANOIC ACID
    2. Synonyms: 6-chloro-hexanoicaci;6-CHLOROCAPROIC ACID;6-CHLOROHEXANOIC ACID;6-CHLORO-N-HEXANOIC ACID;6-CHLORO-N-CAPROIC ACID;Chlorohexanoicacid;6-CHLORO-N-HEXANOIC ACID 98+%;Hexanoic acid, 6-chloro-
    3. CAS NO:4224-62-8
    4. Molecular Formula: C6H11ClO2
    5. Molecular Weight: 150.6
    6. EINECS: N/A
    7. Product Categories: Organic acids;omega-Chlorocarboxylic Acids;omega-Functional Alkanols, Carboxylic Acids, Amines & Halides
    8. Mol File: 4224-62-8.mol
  • Chemical Properties

    1. Melting Point: 26°C
    2. Boiling Point: 138-140℃ (10 Torr)
    3. Flash Point: 26 °C
    4. Appearance: /
    5. Density: 1.127 g/cm3
    6. Refractive Index: 1.4680 (589.3 nm 20℃)
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. PKA: 4.73±0.10(Predicted)
    10. CAS DataBase Reference: 6-CHLORO-N-HEXANOIC ACID(CAS DataBase Reference)
    11. NIST Chemistry Reference: 6-CHLORO-N-HEXANOIC ACID(4224-62-8)
    12. EPA Substance Registry System: 6-CHLORO-N-HEXANOIC ACID(4224-62-8)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: 34
    3. Safety Statements: 26-36/37/39-45
    4. RIDADR: 3265
    5. WGK Germany:
    6. RTECS: MO7000000
    7. HazardClass: 8
    8. PackingGroup:
    9. Hazardous Substances Data: 4224-62-8(Hazardous Substances Data)

4224-62-8 Usage

Uses

Used in Chemical Synthesis:
6-CHLORO-N-HEXANOIC ACID is used as an intermediate in the chemical synthesis of other compounds, playing a crucial role in the production of various chemical products.
Used in Polymer Production:
6-CHLORO-N-HEXANOIC ACID is used as a building block in the production of polymers, contributing to the formation of complex molecular structures with specific properties.
Used in Resin Manufacturing:
6-CHLORO-N-HEXANOIC ACID is used as a component in resin manufacturing, where it helps in creating resins with desired characteristics for various applications.
Safety Considerations:
Due to its potentially corrosive effects, the handling and disposal of 6-Chloro-N-hexanoic acid should be done with caution to ensure safety and prevent environmental harm.

Check Digit Verification of cas no

The CAS Registry Mumber 4224-62-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,2 and 4 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4224-62:
(6*4)+(5*2)+(4*2)+(3*4)+(2*6)+(1*2)=68
68 % 10 = 8
So 4224-62-8 is a valid CAS Registry Number.

4224-62-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-Chlorohexanoic acid

1.2 Other means of identification

Product number -
Other names 6-CHLORO-N-HEXANOIC ACID

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:4224-62-8 SDS

4224-62-8Relevant articles and documents

Solid-state chlorodecarboxylation of mono- and dicarboxylic acids with the Pb(OAc)4-MCl system

Nikishin,Sokova,Chizhov,Makhaev,Kapustina

, p. 2200 - 2204 (2007/10/03)

Solid state reactions of acids RCOOH (R = n-C7H15, BuC(Et)H, n-C9H19, PhCH2, PhCH 2CH2, H2C=CH(CH2)8, or MeOOC(CH2)3) with Pb(OAc)4 combined with KCl, NaCl, CdCl2, or NH4Cl in the absence of a solvent and without mechanical activation afford chlorohydrocarbons RCl. The corresponding reactions of acids HOOC(CH2)nCOOH (n = 3-6) give dichloroalkanes Cl(CH2)nCl and γ-butyrolactone (n = 3).

Decyclization of chlorocyclohexanone hydroperoxides under the action of ferrous salts

Starostin,Gushchin,Ignatenko,Aleksandrov,Nikishin

, p. 133 - 136 (2007/10/03)

The decomposition of 2-chloro-, 2,2-dichloro-, and 2,6-dichloro-substituted cyclohexanone hydroperoxides on treatment with ferrous chloride and sulfate to give chloro-substituted aliphatic acids was investigated. A method for the synthesis of 2,6,6-trichlorohexanoic and 2,6,7,11-tetrachlorododecane-1,12-dioic acids was elaborated.

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