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6-Methylcoumarin

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6-Methylcoumarin Basic information

Product Name:
6-Methylcoumarin
Synonyms:
  • 6-MC
  • 6-Methyl-1,2-benzopyrone
  • 6-methyl-2h-1-benzopyran-2-on
  • 6-methyl-2H-1-Benzopyran-2-one
  • 6-Methyl-2-oxo-2H-benzopyran
  • 6-Methyl-2-oxochronene
  • 6-Methyl-chromen-2-one
  • 6-methyl-coumari
CAS:
92-48-8
MF:
C10H8O2
MW:
160.17
EINECS:
202-158-8
Product Categories:
  • Building Blocks
  • Heterocyclic Building Blocks
  • Alphabetical Listings
  • Flavors and Fragrances
  • M-N
  • Building Blocks
  • Pharmaceutical Raw Materials
  • Coumarins
  • Miscellaneous
  • Chemical Synthesis
  • Heterocyclic Building Blocks
Mol File:
92-48-8.mol
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6-Methylcoumarin Chemical Properties

Melting point:
73-76 °C (lit.)
Boiling point:
303 °C/725 mmHg (lit.)
Density 
1.0924 (rough estimate)
refractive index 
1.5300 (estimate)
FEMA 
2699 | 6-METHYLCOUMARIN
Flash point:
303°C/725mm
storage temp. 
Sealed in dry,Room Temperature
solubility 
DMSO : ≥ 125 mg/mL (780.42 mM)
form 
powder to crystal
color 
White to Almost white
Odor
at 1.00 % in dipropylene glycol. coconut creamy powdery coumarinic tonka cinnamyl vanilla floral earthy
Odor Type
coconut
JECFA Number
1172
BRN 
4222
LogP
1.85
CAS DataBase Reference
92-48-8(CAS DataBase Reference)
NIST Chemistry Reference
2H-1-Benzopyran-2-one, 6-methyl-(92-48-8)
EPA Substance Registry System
6-Methylcoumarin (92-48-8)
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22-42/43
Safety Statements 
22-36/37-45
WGK Germany 
3
RTECS 
GN7792000
TSCA 
Yes
HS Code 
29321900
Hazardous Substances Data
92-48-8(Hazardous Substances Data)
Toxicity
The acute oral LD50 value in rats was reported to be 1.68 g/kg (1.43-1.93 g/kg) (Moreno, 1973). The acute dermal LD50 value in rabbits exceeded 5 g/kg (Moreno, 1973).

MSDS

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6-Methylcoumarin Usage And Synthesis

Chemical Properties

6-methylcoumarin is a white to almost white crystalline powder with has a somewhat coconut-like odor. the odor is also characterized as having a delicate fig or date sweetness. it has an almost bitter taste above 50 ppm, turning sweet and vanilla-like at lower levels. soluble in benzene, hot ethanol and non-volatile oil, insoluble in hot water.

Occurrence

Has apparently not been reported to occur in nature

Uses

6-Methylcoumarin is a synthetic fragrance in cosmetics, toiletries and soaps. It mainly used to prepare flavors such as coconut, vanilla and caramel.

Preparation

6-methylcoumarin is synthesized from p-cresol and fumaric acid. Preheat 72% sulfuric acid to 80 °C, add a mixture of fumaric acid and p-cresol, keep the reaction at 160-170 °C for 3-4 hours, cool, pour into crushed ice to precipitate a precipitate, and filter. The filtrate was extracted with benzene, and after adding benzene, the obtained crude product was subjected to vacuum distillation to obtain 6-methylcoumarin.
synthesis of 6-methylcoumarin: By heating 6-methyl coumarin-3-carboxylic acid to 300 to 340°C; by condensation of p-cresol-disulfonic acid with fumaric acid in the presence of H2SO4; by condensation of p-homosalicyclic aldehyde with malonic acid in the presence of aniline, followed by heating for the lactone; from salicylaldehyde with propionic acid anhydride and sodium propionate.

Definition

ChEBI: 6-methylcoumarin is a member of the class of coumarins that is coumarin in which the hydrogen at position 6 is replaced by a methyl group. It has a role as a fragrance and an allergen.

Aroma threshold values

Aroma characteristics at 1.0%: sweet vanilla cake, creamy, coconut, coumarin-like and powdery, with herbaceous hay and tonka-like nuances.

Taste threshold values

Taste characteristics at 5 ppm: coconut, sweet vanilla, dairy creamy, hay-like with anisic and coumarin nuances.

Synthesis Reference(s)

Tetrahedron, 62, p. 6918, 2006 DOI: 10.1016/j.tet.2006.04.080

General Description

6-methylcoumarin appears as white crystals with a flavor of vanilla. Insoluble in water. (NTP, 1992)

Air & Water Reactions

Insoluble in water.

Reactivity Profile

Ketones, such as 6-Methylcoumarin, are reactive with many acids and bases liberating heat and flammable gases (e.g., H2). The amount of heat may be sufficient to start a fire in the unreacted portion of the ketone. Ketones react with reducing agents such as hydrides, alkali metals, and nitrides to produce flammable gas (H2) and heat. Ketones are incompatible with isocyanates, aldehydes, cyanides, peroxides, and anhydrides. They react violently with aldehydes, HNO3, HNO3 + H2O2, and HClO4.

Fire Hazard

6-Methylcoumarin is combustible.

Biochem/physiol Actions

Taste at 5 ppm

Safety Profile

Poison by subcutaneous route. Moderately toxic by ingestion. A skin irritant. Mutation data reported. Combustible liquid. When heated to decomposition it emits acrid smoke and irritating fumes.

6-Methylcoumarin Preparation Products And Raw materials

Raw materials

6-MethylcoumarinSupplier

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