Description Reference
ChemicalBook > CAS DataBase List > 2'-Hydroxyacetophenone

2'-Hydroxyacetophenone

Description Reference
Product Name
2'-Hydroxyacetophenone
CAS No.
118-93-4
Chemical Name
2'-Hydroxyacetophenone
Synonyms
2-HYDROXYACETOPHENONE;2-HYDROXYACETAMIDE;1-(2-HYDROXYPHENYL)ETHANONE;O-HYDROXYACETOPHENONE;2-ACETYLPHENOL;usafke-20;FEMA 3548;USAF ke-20;AKOS 90575;2-ACETOPHENOL
CBNumber
CB8421762
Molecular Formula
C8H8O2
Formula Weight
136.15
MOL File
118-93-4.mol
More
Less

2'-Hydroxyacetophenone Property

Melting point:
3-6 °C(lit.)
Boiling point:
213 °C717 mm Hg(lit.)
Density 
1.131 g/mL at 25 °C(lit.)
vapor density 
4.7 (vs air)
vapor pressure 
~0.2 mm Hg ( 20 °C)
refractive index 
n20/D 1.558(lit.)
FEMA 
3548 | 2-HYDROXYACETOPHENONE
Flash point:
>230 °F
storage temp. 
Store below +30°C.
solubility 
0.2g/l
form 
Liquid
pka
10.06(at 25℃)
color 
Clear yellow to brown
Odor
at 10.00 % in dipropylene glycol. phenolic sweet hawthorn tobacco honey herbal
Odor Type
phenolic
biological source
synthetic
explosive limit
0.98-11.8%(V)
Water Solubility 
slightly soluble
JECFA Number
727
BRN 
386123
LogP
1.92-1.97 at 25℃
Dissociation constant
10.06-10.25 at 20-25℃
CAS DataBase Reference
118-93-4(CAS DataBase Reference)
NIST Chemistry Reference
Ethanone, 1-(2-hydroxyphenyl)-(118-93-4)
EPA Substance Registry System
2'-Hydroxyacetophenone (118-93-4)
More
Less

Safety

Hazard Codes 
Xi
Risk Statements 
36/37/38-36/38
Safety Statements 
26-36-37/39
WGK Germany 
3
RTECS 
AM8575000
8
Hazard Note 
Harmful/Irritant
TSCA 
Yes
HS Code 
29145000
Toxicity
LD50 orally in Rabbit: 2127 mg/kg LD50 dermal Rat > 2000 mg/kg
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P304+P340IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P405Store locked up.

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
H18607
Product name
2′-Hydroxyacetophenone
Purity
ReagentPlus , 99%
Packaging
5g
Price
$15.9
Updated
2024/03/01
Sigma-Aldrich
Product number
8.04310
Product name
2′-Hydroxyacetophenone
Purity
for synthesis
Packaging
250ML
Price
$92.5
Updated
2024/03/01
Sigma-Aldrich
Product number
PHR1973
Product name
Acetaminophen Impurity I
Purity
Pharmaceutical Secondary Standards; Certified Reference Material
Packaging
100MG
Price
$388
Updated
2022/05/15
TCI Chemical
Product number
H0192
Product name
2'-Hydroxyacetophenone
Purity
>98.0%(HPLC)(T)
Packaging
25g
Price
$25
Updated
2024/03/01
TCI Chemical
Product number
H0192
Product name
2'-Hydroxyacetophenone
Purity
>98.0%(HPLC)(T)
Packaging
100g
Price
$48
Updated
2024/03/01
More
Less

2'-Hydroxyacetophenone Chemical Properties,Usage,Production

Description

2'-Hydroxyacetophenone is a flavouring ingredient. It is a typical flavour additive for cherry kernel, cinnamon, rum, tobacco, coumarin, and tropical fruit. Moreover, it can be used as the intermediate or raw material in organic synthesis. Specifically, this chemical may act as the raw material to prepare a Schiff's base al-alkoxide initiator that facilitates the controlled polymerization of DL-lactide.1 This substance can also function as the effective component in balsamic compounds for fabricating taste modifying compositions.2 Additionally, this chemical has been employed to react with benzoyl chloride for generating 2-(2-Amino-3-methoxyphenyl)-4-oxo-4H-[1]benzopyran, which exhibits good performance for treating cancer and other proliferative diseases such as psoriasis and restenosis.3

Reference

  1. Bhaw-Luximon, A.; Jhurry, D.; Spassky, N., Controlled polymerization of DL-lactide using a Schiff's base al-alkoxide initiator derived from 2-hydroxyacetophenone. Polym. Bull. 2000, 44, 31-38.
  2. Johann Wonschick; Clemens M. Putter; Keepe, E., TASTE MODIFYING COMPOSITIONS PCT WO 2016/103183 A1 2016.
  3. Alexander J Bridges; Saltiel, A. R., 2-(2-Amino-3-methoxyphenyl)-4-oxo-4H-[1]benzopyran for treating proliferative disorders US Patent US5525625 1996.

Chemical Properties

2-Hydroxyacetophenone is a clear yellow to brown liquid that has a sweet, heavy floral, herbaceous odor, reminiscent of mown hay or hawthorn.

Occurrence

Reported found in beef, cassia oil, cocoa, cocoa powder, coffee, Jamaican rum, tomato, Scotch whiskey, sherry, tea, mountain papaya, papaya, roasted almond and black choke berry

Uses

2'-Hydroxyacetophenone is used as pharmaceutical intermediate.

Uses

2’Hydroxyacetophenone is a phenolic compound used in the synthesis of potential anti-myobacterial and anticancer agents.

Definition

ChEBI: 2'-Hydroxyacetophenone is a monohydroxyacetophenone that is acetophenone in which one of the hydrogens ortho to the acetyl group has been replaced by a hydroxy group. It has a role as a flavouring agent. It is a monohydroxyacetophenone and a member of phenols.

Preparation

Preparation by Fries rearrangement of phenyl acetate, with Lewis acids aluminium chloride.

Aroma threshold values

Detection: 5.5 ppm; aroma characteristics at 2.0%: phenolic, sharp, benzaldehyde, cherry pit, tropical, melon with a tobacco afternote

Taste threshold values

Taste characteristics at 5.0 ppm: naphthyl, cinnamon, cherry pit, coumarin, phenolic, tobacco and honey.

Synthesis Reference(s)

Tetrahedron Letters, 24, p. 377, 1983 DOI: 10.1016/S0040-4039(00)81412-4

General Description

2'-Hydroxyacetophenone, also known as O-acetylphenol, belongs to the class of organic compounds known as alkyl-phenylketones. These are aromatic compounds containing a ketone substituted by one alkyl group, and a phenyl group. 2'-Hydroxyacetophenone is a sweet, hawthorne, and herbal tasting compound. 2'-Hydroxyacetophenone has been detected, but not quantified in, several different foods, such as green tea, arabica coffees (Coffea arabica), chinese cinnamons (Cinnamomum aromaticum), cocoa beans (Theobroma cacao), and cocoa and cocoa products. This could make 2'-hydroxyacetophenone a potential biomarker for the consumption of these foods.

More
Less

2'-Hydroxyacetophenone Suppliers

GLR Innovations
Tel
+91 9891111994
Email
info@glrgroup.in
Country
India
ProdList
4535
Advantage
58
TCI Chemicals (India) Pvt. Ltd.
Tel
--
Fax
--
Email
sales-in@tcichemicals.com
Country
India
ProdList
6768
Advantage
58
Dr Prem's Molecules Pvt. Ltd.
Tel
--
Fax
--
Email
prem@dpmolecules.com
Country
India
ProdList
544
Advantage
50
Sisco Research Laboratories Pvt. Ltd.
Tel
--
Fax
--
Email
marketing@srlchem.com
Country
India
ProdList
4315
Advantage
58
SREE SYNERIC LAB
Tel
--
Fax
--
Country
India
ProdList
328
Advantage
58
Triveni chemicals
Tel
--
Fax
--
Email
sales@trivenichemical.com
Country
India
ProdList
6088
Advantage
58
Alfa Aesar
Tel
--
Fax
--
Email
tech@alfa.com
Country
India
ProdList
6905
Advantage
58
Santo Righello Pvt. Ltd
Tel
--
Fax
--
Email
marketing@santorighello.com
Country
India
ProdList
918
Advantage
58
Anant Pharmaceuticals Pvt. ltd
Tel
--
Fax
--
Email
info@anantlabs.com
Country
India
ProdList
736
Advantage
58
Oxford laboratories
Tel
--
Fax
--
Country
India
ProdList
652
Advantage
58
JSK Chemical
Tel
--
Fax
--
Email
jsk.chemicals@gmail.com
Country
India
ProdList
291
Advantage
58
Reax Chemicals
Tel
--
Fax
--
Country
India
ProdList
4217
Advantage
58
Medvance Solution
Tel
--
Fax
--
Email
info@medvancesolutions.com
Country
India
ProdList
137
Advantage
58
Dr Chindepalli
Tel
--
Fax
--
Email
Dr.Chindepalli@gmail.com
Country
India
ProdList
486
Advantage
58
BrmoChem
Tel
--
Fax
--
Country
India
ProdList
70
Advantage
58
Pharma Affiliates
Tel
--
Fax
--
Email
@pharmaffiliates.com
Country
India
ProdList
6754
Advantage
58
Earthchem Laboratories P. Ltd.
Tel
--
Fax
--
Email
info@earthchemlab.com
Country
India
ProdList
37
Advantage
58
Sisco Resech Laboratories Private Limited
Tel
--
Fax
--
Country
India
ProdList
655
Advantage
58
Opulent Pharma
Tel
--
Fax
--
Country
India
ProdList
810
Advantage
58
ASM Organics
Tel
--
Fax
--
Country
India
ProdList
1185
Advantage
58
Clearsynth Labs
Tel
--
Fax
--
Email
fo@clearsynth.com
Country
India
ProdList
3887
Advantage
58
Vyshno Bio Sciences
Tel
--
Fax
--
Email
info@vyshnobio.com
Country
India
ProdList
239
Advantage
58
Azole Rasayanas India Private Limited
Tel
--
Fax
--
Email
info@azolerasayanas.com
Country
India
ProdList
681
Advantage
58
Sris Pharmaceuticals
Tel
--
Fax
--
Email
marketing@srispharma.co.in
Country
India
ProdList
130
Advantage
58
Oceanic Pharmachem Pvt. Ltd.
Tel
--
Fax
--
Email
info@oceanicpharmachem.com
Country
India
ProdList
2005
Advantage
58
Doctor Lifeline Remedies India Limited
Tel
--
Fax
--
Country
India
ProdList
22
Advantage
58
Anant Pharmaceuticals Pvt., Ltd.
Tel
--
Fax
--
Email
sales@anantlabs.com
Country
India
ProdList
160
Advantage
58
Anand Agencies
Tel
--
Fax
--
Email
en@gmail.com
Country
India
ProdList
2332
Advantage
58
Loba Chemie Pvt Ltd
Tel
--
Fax
--
Country
India
ProdList
498
Advantage
58
Labort Fine Chem Pvt. Ltd
Tel
--
Fax
--
Country
India
ProdList
76
Advantage
58
SynZeal Research Pvt Ltd
Tel
--
Fax
--
Email
standards@synzeal.com
Country
India
ProdList
6514
Advantage
58
Brom-Chem
Tel
--
Fax
--
Country
India
ProdList
62
Advantage
58
Saisri Hetero Cyclics (SSH)
Tel
--
Fax
--
Email
srisai@sriheterocyclics.com
Country
India
ProdList
262
Advantage
58
Zeon Pharma (Div. of Zeon. Health Ind.)
Tel
--
Fax
--
Email
info@zeonpharma.com
Country
India
ProdList
38
Advantage
58
Avra Synthesis Pvt Ltd
Tel
--
Fax
--
Email
info@avrasynthesis.com
Country
India
ProdList
1603
Advantage
30
Molecraft LifeSciences Pvt Ltd
Tel
--
Fax
--
Email
info@molecraft.com
Country
India
ProdList
757
Advantage
0
PEE ESS AROMATICS
Tel
--
Fax
--
Email
peeessaroma@yahoo.com
Country
India
ProdList
258
Advantage
30
Meru Chem Pvt. Ltd.
Tel
--
Fax
--
Email
meruchempltd@gmail.com
Country
India
ProdList
174
Advantage
58
Jamunesh Imex
Tel
--
Fax
--
Country
India
ProdList
5
Advantage
58
G.c.intl
Tel
--
Fax
--
Country
India
ProdList
105
Advantage
58
Pharmaffiliates Analytics and Synthetics P. Ltd
Tel
--
Fax
--
Email
mktg@pharmaffiliates.com
Country
India
ProdList
6739
Advantage
58
Central Drug House(P) Ltd.
Tel
--
Fax
--
Email
sales@cdhfinechemical.com
Country
India
ProdList
6157
Advantage
58
A.J Chemicals
Tel
--
Fax
--
Email
sales@ajchem.in
Country
India
ProdList
6100
Advantage
58
CHEMSWORTH
Tel
--
Fax
--
Email
info@chemsworth.com
Country
India
ProdList
6700
Advantage
30
Daga Global Chemicals Co., Ltd
Tel
--
Fax
--
Email
kolkata@dagaglobal.com
Country
India
ProdList
11
Advantage
63
Dr. Jagath Reddy's Heterocyclics
Tel
--
Fax
--
Email
jagathreddy@usa.net
Country
India
ProdList
3886
Advantage
42
ALPHA CHEMIKA
Tel
--
Fax
--
Email
info@exporterlabchemicals.com
Country
India
ProdList
1679
Advantage
43
Scientific OEM
Tel
--
Fax
--
Email
neeraj@scientificoem.com
Country
India
ProdList
1994
Advantage
38
BASR Fine Chemicals
Tel
--
Fax
--
Email
info@basrtech.com
Country
India
ProdList
237
Advantage
56
OCEAN TRADING CORPORATION
Tel
--
Fax
--
Email
otcchem@otcchem.com
Country
India
ProdList
6202
Advantage
58
More
Less

View Lastest Price from 2'-Hydroxyacetophenone manufacturers

Shandong Deshang Chemical Co., Ltd.
Product
2'-Hydroxyacetophenone 118-93-4
Price
US $8.80-6.20/kg
Min. Order
1kg
Purity
99%
Supply Ability
10 tons
Release date
2024-07-05
Hebei Weibang Biotechnology Co., Ltd
Product
2'-Hydroxyacetophenone 118-93-4
Price
US $10.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
10 mt
Release date
2024-10-29
Hebei Yanxi Chemical Co., Ltd.
Product
2-Hydroxyacetophenone 118-93-4
Price
US $40.00/kg
Min. Order
1kg
Purity
0.99
Supply Ability
10 tons
Release date
2023-09-18

118-93-4, 2'-HydroxyacetophenoneRelated Search:


  • 1-(2-hydroxyphenyl)-ethanon
  • o-hydroxyphenylmethylketone
  • USAF ke-20
  • usafke-20
  • AKOS 90575
  • AKOS BBS-00003239
  • 2-HYDROXYPHENYL METHYL KETONE
  • 2'-HYDROXYACETOPHENONE
  • 2-HYDROXYACETOPHENONE
  • 2-ACETYLPHENOL
  • 2-ACETOPHENOL
  • FEMA 3548
  • 1-(2-HYDROXYPHENYL)ETHANONE
  • O-HYDROXYACETOPHENONE
  • O-ACETOPHENOL
  • Acetaminophen impurity 9
  • Paracetamol EP Impurity I
  • Acetaminophen Impurity I
  • Paracetamol Impurity 9(Paracetamol EP Impurity I)
  • Acetophenone, o-hydroxy-
  • Ethanone,1-(2-hydroxyphenyl)-
  • o-Acetylphenol
  • o-hydroxy-acetophenon
  • o-Hydroxyphenyl methyl ketone
  • 2'-Hydorxyacetophenone 1-(2-Hydroxyphenyl)ethanone 2-Acetylphenol
  • 2'-HYDROXYACETOPHENONE 98+%
  • 2'-Hydorxyacetophenone
  • 2’-hydroxy-acetophenon
  • 2-hydroxyacetylbenzene
  • Ethanone,1-(2-hydroxypheny
  • 2''-HYDROXYACETOPHENONE 99+%
  • 2-HYDROXYACETAMIDE
  • BENZOYLCARNINOL
  • o-HYDROXYACETOPHENONE pure
  • 2′-Hydroxyacetophenone,2-Acetylphenol
  • 2'-Hydroxyacetopheno
  • 2-Acetophenol 2-Acetylphenol 2-Hydroxyphenyl Methyl Ketone
  • 2'-HYDROXYACETOPHENONE FOR SYNTHESIS
  • 1-(2-Hydroxyphenyl)ethan-1-one, 2-Acetylphenol, 1-(2-Hydroxyphenyl)-1-oxoethane
  • ParacetaMol IMpurity I
  • 2'-Hydroxyacetophenone ReagentPlus(R), 99%
  • 2'-Hydroxyacetophenone Vetec(TM) reagent grade, 98%
  • Acetaminophen Impurity 12
  • 1-(6-hydroxy-1-cyclohexa-2,4-dienyl)ethanone
  • Paracetamol EP Impurity I( 2'-Hydroxyacetophenone)
  • hydroxyacetophenone,o-hydroxyacetophenone
  • 2'-Hydroxyacetophenone, 99%, for synthesis
  • 1-(2-Hydroxyphenyl)ethanone (2-Hydr
  • 2'-Hydroxyacetophenone&gt
  • Paracetamol(Acetaminophen) EP Impurity I
  • Acetaminophen impurities1463
  • Acetaminophen EP Impurity I
  • Paracetamol Impurity I(EP)
  • Potassium 4-methoxysalicylate 152312-71-5
  • 2'-Hydroxyacetophenone
  • Paracetamol EP Impurity I 1-(2-hydroxyphenyl)ethan-1-one
  • Ortho-Hydroxyacetophenone/2'-Hydroxyacetophenone
  • 2''-Hydroxyacetophenone, 10 mM in DMSO