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2,4-Dihydroxyacetophenone

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CAS:89-84-9
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CAS:89-84-9
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CAS:89-84-9
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CAS:89-84-9
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CAS:89-84-9
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2,4-Dihydroxyacetophenone manufacturers

  • 4-Acetylresorcinol
  • 4-Acetylresorcinol pictures
  • $10.00 / 1kg
  • 2024-04-22
  • CAS:89-84-9
  • Min. Order: 1kg
  • Purity: 99.6%
  • Supply Ability: 100000
2,4-Dihydroxyacetophenone Basic information
Product Name:2,4-Dihydroxyacetophenone
Synonyms:Resoacetophenone;Resorcinol, 4-acetyl-;2,4-Dihydroxyacetoph;NSC 10883;NSC 37559;4-Acetylresorcinol Resacetophenone;IMp. A (EP): 1,3-Dihydroxybenzene (Resorcinol);IMp. B (EP): 7-Hydroxy-2-Methyl-4H-1-benzopyran-4-one
CAS:89-84-9
MF:C8H8O3
MW:152.15
EINECS:201-945-3
Product Categories:Aromatics;Miscellaneous Reagents;Aromatic Acetophenones & Derivatives (substituted);Benzene series;Acetophenone Series;89-84-9;bc0001;john's
Mol File:89-84-9.mol
2,4-Dihydroxyacetophenone Structure
2,4-Dihydroxyacetophenone Chemical Properties
Melting point 143-144.5 °C(lit.)
Boiling point 234.6°C (rough estimate)
density 1.18 g/mL at 25 °C(lit.)
refractive index 1.4945 (estimate)
storage temp. Inert atmosphere,Room Temperature
solubility DMSO (Slightly), Methanol (Slightly)
pka7.96±0.18(Predicted)
form Crystalline Powder or Crystals
color Off-white to pink to brown
PH5 (1g/l, H2O, 20℃)
Sensitive Moisture Sensitive
Merck 14,8140
BRN 1282505
InChIKeySULYEHHGGXARJS-UHFFFAOYSA-N
LogP1.480 (est)
CAS DataBase Reference89-84-9(CAS DataBase Reference)
NIST Chemistry ReferenceEthanone, 1-(2,4-dihydroxyphenyl)-(89-84-9)
EPA Substance Registry SystemEthanone, 1-(2,4-dihydroxyphenyl)- (89-84-9)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36-24/25
WGK Germany 2
RTECS AM7525000
Hazard Note Irritant
TSCA Yes
HS Code 29145000
MSDS Information
ProviderLanguage
Resacetophenone English
SigmaAldrich English
ACROS English
ALFA English
2,4-Dihydroxyacetophenone Usage And Synthesis
Chemical Properties2,4-Dihydroxyacetophenone appears as a yellow-brown to reddish-brown fine crystalline powder. It slowly decomposes in water and can dissolve in hot alcohol, pyridine, and glacial acetic acid. In contrast, it is nearly insoluble in ether, benzene, and chloroform. A reaction with iron chloride causes it to adopt a red hue.
Uses2,4-Dihydroxyacetophenone (cas# 89-84-9) is a compound useful in organic synthesis. It is also used as intermediate for pharmaceuticals. Reagent for iron as a 10% alcoholic solution. A red color is obtained with ferric ions in slightly acid solution: Cooper, Ind. Eng. Chem. Anal. Ed. 9, 334 (1937).
PreparationPreparation by reaction of acetic acid on resorcinol,
with zinc chloride (Nencki reaction) (94%)
with boron trifluoride
with Amberlite IR-120 (a cation exchange resin, sulfonic acid type) (87%)
with polyphosphoric acid (63%)
with 70% perchloric acid (33%).
DefinitionChEBI: 2',4'-dihydroxyacetophenone is a dihydroxyacetophenone that is acetophenone carrying hydroxy substituents at positions 2' and 4'. It has a role as a plant metabolite. It is a member of resorcinols and a dihydroxyacetophenone.
Synthesis Reference(s)Journal of the American Chemical Society, 70, p. 428, 1948 DOI: 10.1021/ja01181a521
Safety ProfileModerately toxic by ingestion. Experimental reproductive effects. A severe eye irritant. When heated to decomposition it emits acrid smoke and irritating fumes.
Synthesis2,4-Dihydroxyacetophenone is obtained by the acetylation of resorcinol and acetic acid. In addition, it can also be obtained by reacting resorcinol with chloroacetyl or acetic anhydride in the presence of zinc chloride.
targetPhospholipase (e.g. PLA)
Tag:2,4-Dihydroxyacetophenone(89-84-9) Related Product Information
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