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6-Bromohexanoic acid

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6-Bromohexanoic acid manufacturers

  • 6-Bromohexanoic acid
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  • $1.00
  • 2026-09-11
  • CAS:4224-70-8
  • Min. Order: 1KG
  • Purity: 99%
  • Supply Ability: 1000kg/month
  • 6-Bromohexanoic acid
  • 6-Bromohexanoic acid pictures
  • $30.00
  • 2026-08-07
  • CAS:4224-70-8
  • Min. Order: 1KG
  • Purity: 99%
  • Supply Ability: 200000KG

Related articles

  • Preparation of 6-Bromocaproic Acid
  • 6-Bromohexanoic acid is used in the preparation of N-acylsulfonamides, diarylthioethers and 2-lithio-1,3-dithian. It is widely....
  • Dec 20,2019
6-Bromohexanoic acid Basic information
Organic Intermediate
Product Name:6-Bromohexanoic acid
Synonyms:6 - broMine caproic acid;6-BroMhexine acid;6-BroMhexanoic acid;ω-BroMohexanoic Αcid;6-BroMohexanoic acid, 98% 25GR;ISBO-007;6-bromo-hexanoicaci;6-Bromo-n-caproic acid
CAS:4224-70-8
MF:C6H11BrO2
MW:195.05
EINECS:224-176-5
Product Categories:Carbonyl Compounds;Carboxylic Acids;Chemical Synthesis;Organic Building Blocks;omega-Functional Alkanols, Carboxylic Acids, Amines & Halides;Aliphatics;Miscellaneous Reagents;Building Blocks;Organic acids;Acids & Esters;Bromine Compounds;omega-Bromocarboxylic Acids;C6
Mol File:4224-70-8.mol
6-Bromohexanoic acid Structure
6-Bromohexanoic acid Chemical Properties
Melting point 32-34 °C (lit.)
Boiling point 165-170 °C/20 mmHg (lit.)
density 1.3996 (rough estimate)
refractive index 1.4790 (estimate)
Fp 154 °F
storage temp. Inert atmosphere,2-8°C
solubility methanol: 0.1 g/mL, clear, colorless
pka4.72±0.10(Predicted)
form Low Melting Crystals
color White to light orange
BRN 1749740
InChI1S/C6H11BrO2/c7-5-3-1-2-4-6(8)9/h1-5H2,(H,8,9)
InChIKeyNVRVNSHHLPQGCU-UHFFFAOYSA-N
SMILESOC(=O)CCCCCBr
LogP1.700 (est)
CAS DataBase Reference4224-70-8(CAS DataBase Reference)
NIST Chemistry ReferenceHexanoic acid, 6-bromo-(4224-70-8)
EPA Substance Registry SystemHexanoic acid, 6-bromo- (4224-70-8)
Safety Information
Hazard Codes C
Risk Statements 34
Safety Statements 26-36/37/39-45-28A
RIDADR UN 3261 8/PG 2
WGK Germany 3
8
Hazard Note Corrosive/Harmful
TSCA TSCA listed
HazardClass 8
PackingGroup III
HS Code 29159080
Storage Class8A - Combustible corrosive hazardous materials
Hazard ClassificationsSkin Corr. 1B
MSDS Information
ProviderLanguage
6-Bromocaproic acid English
SigmaAldrich English
ACROS English
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6-Bromohexanoic acid Usage And Synthesis
Organic Intermediate6-bromohexanoic acid(CAS:4224-70-8), also called 6-bromohexanoic acid or 6-bromo-hexanoic acid, is an organobromine compound comprising hexanoic acid having a bromo substituent at the 6-position. 6-Bromohexanoic acid is used in the preparation of N-acylsulfonamides, diarylthioethers and 2-lithio-1,3-dithian. It is widely used as an intermediate in organic synthesis. Here, we introduced a method for making this compound.
Chemical PropertiesWhite to light orange low melting crystals
UsesEmployed in a direct preparation of N-acylsulfonamides on treatment with tosyl isocyanate (189278)1 and alkyl ketones from alkyl iodides and metallic strontium.2
Uses6-Bromohexanoic acid is used in the preparation of N-acylsulfonamides, diarylthioethers and 2-lithio-1,3-dithian. It is widely used as an intermediate in organic synthesis.
Uses6-Bromohexanoic acid was used in the preparation of N-acylsulfonamides on treatment with tosyl isocyanate (189278) and alkyl ketones from alkyl iodides and metallic strontium. It was also used in the synthesis of anionic mitomycin C-dextran conjugate (MMC-D), 2-lithio-1,3-dithian and diaryl thioethers.
DefinitionChEBI: 6-bromohexanoic acid is an organobromine compound comprising hexanoic acid having a bromo substituent at the 6-position. It is functionally related to a hexanoic acid.
Synthesis Reference(s)Journal of the American Chemical Society, 72, p. 5137, 1950 DOI: 10.1021/ja01167a091
SynthesisThe preparation method of the high purity 6-bromocaproic acid: the exsiccant bromize hydrogen gas is directly fed contain in the organic solvent of 6-caprolactone, exsiccant bromize hydrogen gas usage quantity is 6-caprolactone 1.0-2.0 doubly (mol ratio); Stir, ring-opening reaction takes place, temperature of reaction is 0 ℃ ~ 100 ℃, generates high purity 6-bromocaproic acid.
References[1] Reactive and Functional Polymers, 2016, vol. 99, p. 1 - 8
[2] Bioorganic and Medicinal Chemistry, 2011, vol. 19, # 1, p. 567 - 579
[3] Bioorganic and Medicinal Chemistry, 2006, vol. 14, # 9, p. 2896 - 2903
[4] Bioorganic and Medicinal Chemistry, 2006, vol. 14, # 23, p. 7681 - 7687
[5] Journal of the American Chemical Society, 1982, vol. 104, # 5, p. 1391 - 1403
Tag:6-Bromohexanoic acid(4224-70-8) Related Product Information
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