ChemicalBook--->CAS DataBase List--->89-84-9

89-84-9

89-84-9 Structure

89-84-9 Structure
IdentificationMore
[Name]

2,4-Dihydroxyacetophenone
[CAS]

89-84-9
[Synonyms]

1-ACETYL-2,4-DIHYDROXYBENZENE
2',4'-DIHYDROXYACETOPHENONE
2,4-DIHYDROXYACETOPHENONE
2,4-DIHYDROXY ACETPHENONE
4-ACETYLRESORCINOL
AKOS 90593
AKOS BBS-00004294
RESACETOPHENONE
1-(2,4-dihydroxyphenyl)-ethanon
1-(2,4-dihydroxyphenyl)ethanone
1-(2,4-Dihydroxyphenyl)-ethanone
1-Acetylbenzene-2,4-diol
2’,4’-dihydroxy-acetophenon
4-Acetyl-1,3-benzenediol
4-acetyl-resorcino
Acetophenone, 2',4'-dihydroxy-
beta-Resacetophenone
b-Resacetophenone
Resoacetophenone
Resorcinol, 4-acetyl-
[EINECS(EC#)]

201-945-3
[Molecular Formula]

C8H8O3
[MDL Number]

MFCD00002279
[Molecular Weight]

152.15
[MOL File]

89-84-9.mol
Chemical PropertiesBack Directory
[Appearance]

yellow-brown to reddish-brown fine cryst. powder
[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)
[form ]

Crystalline Powder or Crystals
[pka]

7.96±0.18(Predicted)
[color ]

Off-white to pink to brown
[PH]

5 (1g/l, H2O, 20℃)
[Sensitive ]

Moisture Sensitive
[Merck ]

14,8140
[BRN ]

1282505
[Cosmetics Ingredients Functions]

SKIN CONDITIONING
BLEACHING
ANTIOXIDANT
[InChI]

1S/C8H8O3/c1-5(9)7-3-2-6(10)4-8(7)11/h2-4,10-11H,1H3
[InChIKey]

SULYEHHGGXARJS-UHFFFAOYSA-N
[SMILES]

CC(=O)c1ccc(O)cc1O
[LogP]

1.480 (est)
[CAS DataBase Reference]

89-84-9(CAS DataBase Reference)
[NIST Chemistry Reference]

Ethanone, 1-(2,4-dihydroxyphenyl)-(89-84-9)
[EPA Substance Registry System]

89-84-9(EPA Substance)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H319
[Precautionary statements ]

P264-P280-P305+P351+P338-P337+P313
[Hazard Codes ]

Xi
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing .
S24/25:Avoid contact with skin and eyes .
[WGK Germany ]

2
[RTECS ]

AM7525000
[Hazard Note ]

Irritant
[TSCA ]

Yes
[REACH Registrations]

Active
[HS Code ]

29145000
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Eye Irrit. 2
[Safety Profile]

Moderately toxic by ingestion. Experimental reproductive effects. A severe eye irritant. When heated to decomposition it emits acrid smoke and irritating fumes.
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Zinc chloride
[Preparation Products]

7-Hydroxycoumarin-->1-[4-(Benzoyloxy)-2-hydroxyphenyl]-3-phenyl-1,3-propanedione-->1-(2,4-Bis(benzoyloxy)phenyl)ethanone-->7-Hydroxyflavone-->2',4'-Dihydroxychalcone-->3,7-Dihydroxyflavone-->4-Hydroxy-7-methoxycoumarin-->7-Hydroxyflavanone-->ROBINETIN-->4'-Benzyloxy-2'-hydroxyacetophenone-->4-Ethylresorcinol-->UP302-->2,4-Dimethoxyacetophenone
Material Safety Data Sheet(MSDS)Back Directory
[msds information]

Resacetophenone(89-84-9).msds
Hazard InformationBack Directory
[Chemical Properties]

2,4-Dihydroxyacetophenone(89-84-9) 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.
[Uses]

2,4-Dihydroxyacetophenone is used as intermediate for pharmaceuticals.
[Uses]

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).
[Definition]

ChEBI: A dihydroxyacetophenone that is acetophenone carrying hydroxy substituents at positions 2' and 4'.
[Preparation]

Preparation 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%).
[Synthesis Reference(s)]

Journal of the American Chemical Society, 70, p. 428, 1948 DOI: 10.1021/ja01181a521
[Synthesis]

2,4-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.
[target]

Phospholipase (e.g. PLA)
Spectrum DetailBack Directory
[Spectrum Detail]

2,4-Dihydroxyacetophenone(89-84-9)MS
2,4-Dihydroxyacetophenone(89-84-9)1HNMR
2,4-Dihydroxyacetophenone(89-84-9)IR1
2,4-Dihydroxyacetophenone(89-84-9)Raman
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

2',4'-Dihydroxyacetophenone, 98%(89-84-9)
[Alfa Aesar]

2',4'-Dihydroxyacetophenone, 98%(89-84-9)
[Sigma Aldrich]

89-84-9(sigmaaldrich)
[TCI AMERICA]

2',4'-Dihydroxyacetophenone,>98.0%(GC)(T)(89-84-9)
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