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2′,4′-Dihydroxyacetophenone

2′,4′-Dihydroxyacetophenone structure

CAS No:
89-84-9
Formula:
C8H8O3
Chemical Name:
2′,4′-Dihydroxyacetophenone
Synonyms:
Ethanone,1-(2,4-dihydroxyphenyl)-;Acetophenone,2′,4′-dihydroxy-;1-(2,4-Dihydroxyphenyl)ethanone;Resacetophenone;Resoacetophenone;2′,4′-Dihydroxyacetophenone;β-Resacetophenone;4-Acetylresorcinol;1-Acetylbenzene-2,4-diol;4-Acetyl-1,3-benzenediol;NSC 10883;NSC 37559;2′,4′-Dihydroxyphenyl methyl ketone
Categories:
Cosmetic Ingredient > Bleaching Agent

Description

2',4'-Dihydroxyacetophenone (Resacetophenone) is acetophenone carrying hydroxy substituents at positions 2' and 4'. A plant metabolite.

Solid

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.

2′,4′-Dihydroxyacetophenone Basic Attributes

Molecular Weight：

152.14700

Exact Mass：

152.15

EC Number：

201-945-3

UNII：

UC3V356VZC

NSC Number：

37559|10883

DSSTox ID：

DTXSID4058998

HScode：

2914391000

Characteristics

PSA：

57.53000

XLogP3：

1.7

Appearance：

Solid

Density：

1.18

Melting Point：

146 °C

Boiling Point：

319.3ºC at 760 mmHg

Flash Point：

161.1ºC

Refractive Index：

1.56467 (141.1ºC)

Water Solubility：

1.507e+004 mg/L @ 25 °C (est)

Storage Conditions：

Store in a tightly closed container. Store in a cool, dry, well-ventilated area away from incompatible substances.

Collision Cross Section：

127.2 Å² [M+H]+ [CCS Type: DT, Method: single field calibrated with ESI Low Concentration Tuning Mix (Agilent)]|126.3 Å² [M-H]- [CCS Type: DT, Method: single field calibrated with ESI Low Concentration Tuning Mix (Agilent)]

Safety Information

Transport codes：

NONH for all modes of transport

wgk germany：

hazard class code：

R36/37/38

safety instructions：

S24/25

RTECS Number：

AM7525000

Marks：

Stability/Shelf Life：

Stable at room temperature in closed containers under normal storage and handling conditions.

Precautionary statement(s)：

P261-P280-P305 + P351 + P338

Hazard Statements：

H315-H318-H335

GHS Classification：

|Danger|H315 (97.96%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P310, P312, P321, P332+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 49 companies from 7 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Drug Information

Metabolism/Metabolites：

Resacetophenone has known human metabolites that include 2,4-Dihydroxyacetophenone 5-sulfate.

MeSH Entry Terms：

2,4-dihydroxyacetophenone

2′,4′-Dihydroxyacetophenone Use and Manufacturing

Uses

Reagent for iron as a 10% alcoholic solution.

Manufacturing Info：

Ethanone, 1-(2,4-dihydroxyphenyl)-: ACTIVE

Computed Properties

Molecular Weight:152.15
XLogP3:1.7
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:1
Exact Mass:152.047344113
Monoisotopic Mass:152.047344113
Topological Polar Surface Area:57.5
Heavy Atom Count:11
Complexity:155
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

Synthesis Route

108-24-7

52751-42-5

72712-19-7

Suppliers(1)

Material

Resorcinol

Acetic acid

Sulfuric acid

Downstream Products

Lauric acid

Drug Function and Efficacy

Exhibits anti-inflammatory and antioxidant activities, potentially contributing to skin soothing effects.

This ingredient has been used in drugs with the following functions (note: it does not mean that the ingredient itself has the following health functions)

Related Drugs

DRUGGIST FUNGI NALL- fungi nall_liquid
Manufacturer	Shenzhen Xiaomai Manufacturing Co., Ltd.

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CAS No.: 89-84-9

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Guide of 2′,4′-Dihydroxyacetophenone

Description
Basic Attributes
Characteristics
Safety Information
Drug Information
Use and Manufacturing
Computed Properties
Synthesis Route
Material
Downstream Products
Drug Function and Efficacy
Related Drugs
Recommended Suppliers
Learn More Other Chemicals

2′,4′-Dihydroxyacetophenone

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