Basic information Identification Description Regulatory Status Usage Natural occurrence Safety Supplier Related
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4'-Methoxyacetophenone

Basic information Identification Description Regulatory Status Usage Natural occurrence Safety Supplier Related

4'-Methoxyacetophenone Basic information

Product Name:
4'-Methoxyacetophenone
Synonyms:
  • 4'-Methoxyacetophenone≥ 99% (GC)
  • 4'-Methoxyacetophenone p-Acetanisole 4-Methoxyacetophenone
  • Para Methoxyl Acetophenone
  • ACETANISOLE 98+% FCC
  • 4-Methoxyacetophenone,>99%
  • Epenone
  • P-METHOXY ACETOPLENONE
  • PARA-METHOXYACETONPHENONE
CAS:
100-06-1
MF:
C9H10O2
MW:
150.17
EINECS:
202-815-9
Product Categories:
  • Azetidines
  • Acetophenones (Building Blocks for Liquid Crystals)
  • FINE Chemical & INTERMEDIATES
  • Aromatic Acetophenones & Derivatives (substituted)
  • Building Blocks for Liquid Crystals
  • Functional Materials
  • Acetophenone Series
  • 100-06-1
  • bc0001
Mol File:
100-06-1.mol
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4'-Methoxyacetophenone Chemical Properties

Melting point:
36-38 °C (lit.)
Boiling point:
152-154 °C/26 mmHg (lit.)
Density 
1.08
vapor pressure 
0.42Pa at 20℃
refractive index 
1.5470 (estimate)
FEMA 
2005 | ACETANISOLE
Flash point:
>230 °F
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
solubility 
H2O: soluble2.474g/L at 20°C
form 
Crystals or Crystalline Powder
color 
White
Odor
at 100.00 %. sweet hawthorn anisic powdery balsamic acacia
Odor Type
anisic
Water Solubility 
insoluble
Sensitive 
Light Sensitive
JECFA Number
810
BRN 
742313
InChIKey
NTPLXRHDUXRPNE-UHFFFAOYSA-N
LogP
1.79 at 20℃
CAS DataBase Reference
100-06-1(CAS DataBase Reference)
NIST Chemistry Reference
Acetophenone, 4'-methoxy-(100-06-1)
EPA Substance Registry System
4'-Methoxyacetophenone (100-06-1)
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22-38-36/38-20/21/22
Safety Statements 
37-37/39-26-36
WGK Germany 
2
RTECS 
AM9240000
TSCA 
Yes
HS Code 
29145000
Hazardous Substances Data
100-06-1(Hazardous Substances Data)
Toxicity
The acute oral LD50 value in rats was reported as 1.72 g/kg (1.47-1.97 g/kg) (Moreno, 1973). The acute dermal LD50 value in rabbits was reported as > 5 g/kg (Moreno, 1973).

MSDS

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4'-Methoxyacetophenone Usage And Synthesis

Identification

CAS.No.: 
100-06-1 
FL.No.: 
7.038
FEMA.No.: 
2005
NAS.No.: 
2005
CoE.No.: 
570
EINECS.No.: 
202-815-9 
JECFA.No.: 
810
 
 

Description

Yellowish-white crystals with an odor similar to that of p-methylacetopheneone, suggestive of hawthorn and floral note of heliotrope, possessing a bitter and unpleasant taste. Useful in vanilla, nut, tobacco and butter flavors.

Regulatory Status

CoE: Approved. Bev.: 10 ppm; Food: 20 ppm
FDA: 21 CFR 172.515
FDA (other): n/a
JECFA: ADI: Acceptable. No safety concern at current levels of intake when used as a flavoring agent (2001).

Usage

Reported uses (ppm): (FEMA, 1994)

Food Category 
Usual 
Max. 
Alcoholic.beverages 
0.0001
0.0001
Baked.goods 
1.5
2
Chewing.gum 
110
110
Frozen.dairy 
1
2
Gelatins,.puddings 
0.2
0.2
Hard.candy 
278.3
335
Meat.products 
100
100
Nonalcoholic.beverages 
7.8
150
Soft.candy 
2.1
31

Natural occurrence

Reported found in European cranberry (Vaccinium oxycoccus L.), guava fruit (Psidium guajava L.), Vitis labrusca L., tomato, anise (Pimpinella anisum L.), mentha oils, grilled and roasted beef, sherry, cloudberry (Rubus chamaemorus L.), salted and pickled plums, Illicium verum and black chokeberry (Aronia melanocarpa ell.).

Chemical Properties

WHITE CRYSTALS OR CRYSTALLINE POWDER

Chemical Properties

4-Methoxyacetophenone occurs in anise oil. It forms white crystals (mp 38°C) with a sweet odor, reminiscent of hawthorn. 4-Methoxyacetophenone is prepared by Friedel–Crafts acetylation of anisole. A modern process uses ??-zeolites as Friedel–Crafts catalysts in combination with a continuous flow technology. 4-Methoxyacetophenone is used in soap perfumes

Chemical Properties

Yellowish-white crystals with an odor similar to that of p-methylacetopheneone, suggestive of hawthorn and floral note of heliotrope, possessing a bitter and unpleasant taste. Useful in vanilla, nut, tobacco and butter flavors

Occurrence

Reported found in European cranberry (Vaccinium oxycoccus L.), guava fruit (Psidium guajava L.), Vitis labrusca L., tomato, anise (Pimpinella anisum L.), mentha oils, grilled and roasted beef, sherry, cloudberry (Rubus chamaemorus L.), salted and pickled plums, Illicium verum and black chokeberry (Aronia melanocarpa ell.).

Uses

4'-Methoxyacetophenone is used as a component of perfumes and as chemical intermediate in the manufacture of pharmaceuticals, resins, flavouring agents. And also used to study ruthenium catalyzed step growth copolymerization of 4?-methoxyacetophenone with α,ω-dienes to yield copolymers.

Uses

4'-Methoxyacetophenone is a solid, pale yellow flavoring agent with a hawthornlike odor. It is soluble in most fixed oils and propylene glycol, and it is insoluble in glycerin and mineral oil. It is obtained by chemical synthesis. This flavoring substance or its adjuvant may be safely used in food in the minimum quantity required to produce its intended flavor. It can be used alone or in combination with other flavoring substances or adjuvants. It is also termed p-methoxyacetophenone.

Uses

Perfumery (for floral odors), flavoring.

Definition

ChEBI: A member of the class of acetophenones that is acetophenone substituted by a methoxy group at position 4.

Preparation

From anisole and acetyl chloride in the presence of aluminum chloride and carbon disulfide; from anisole and acetic acid in the presence of boron trifluoride.

Taste threshold values

Taste characteristics at 10 ppm: sweet, anisic, fruity, cherry with powdery vanilla nuances.

Synthesis Reference(s)

The Journal of Organic Chemistry, 46, p. 5414, 1981 DOI: 10.1021/jo00339a036
Synthetic Communications, 26, p. 291, 1996 DOI: 10.1080/00397919608003617
Tetrahedron Letters, 35, p. 9471, 1994 DOI: 10.1016/S0040-4039(00)78574-1

General Description

4′-Methoxyacetophenone undergoes biocatalytic enantioselective reduction using immobilized Rhodotorula sp. AS2.2241 cells to yield (S)-1-(4-methoxyphenyl) ethanol in a hydrophilic ionic liquid-containing co-solvent system.

Flammability and Explosibility

Not classified

Safety Profile

Moderately toxic by ingestion. Human systemic effects by inhalation: pulse rate increase without fall in blood pressure and blood pressure elevation. A skin irritant. Flammable liquid. When heated to decomposition it emits acrid smoke and irritating fumes. See also KETONES.

Purification Methods

Crystallise the ketone from diethyl ether/pet ether. [Beilstein 8 IV 340.]

4'-MethoxyacetophenoneSupplier

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