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ChemicalBook >> CAS DataBase List >>Methyl anthranilate

Methyl anthranilate

CAS No.
134-20-3
Chemical Name:
Methyl anthranilate
Synonyms
METHYL 2-AMINOBENZOATE;Methyl antranilate;NEROLI;Nevoli oil;Methyl anthranylate;o-Carbomethoxyaniline;ANTHRANILIC ACID METHYL ESTER;2-amino-benzoicacimethylester;2-AMINOBENZOIC ACID METHYL ESTER;FEMA 2682
CBNumber:
CB0722306
Molecular Formula:
C8H9NO2
Molecular Weight:
151.16
MDL Number:
MFCD00007710
MOL File:
134-20-3.mol
MSDS File:
SDS
Last updated:2024-12-18 13:37:16

Methyl anthranilate Properties

Melting point 24 °C (lit.)
Boiling point 256 °C (lit.)
Density 1.168 g/mL at 25 °C (lit.)
vapor pressure 1 mm Hg ( 20 °C)
refractive index n20/D 1.582(lit.)
FEMA 2682 | METHYL ANTHRANILATE
Flash point 220 °F
storage temp. Keep in dark place,Inert atmosphere,Room temperature
solubility alcohol: freely soluble(lit.)
pka pK1:2.23(+1) (25°C)
form Liquid
color Clear yellow-brown
PH 7.5-8 (H2O, 20℃)Aqueous solution
Odor grape odor
Odor Type fruity
Viscosity 7.14mm2/s
explosive limit 1.4-7.8%(V)
Water Solubility slightly soluble
Sensitive Air Sensitive
Merck 14,6020
JECFA Number 1534
BRN 606965
Stability Stable. Combustible. Incompatible with strong oxidizing agents.
InChIKey VAMXMNNIEUEQDV-UHFFFAOYSA-N
LogP 1.88 at 20℃
Substances Added to Food (formerly EAFUS) METHYL ANTHRANILATE
FDA 21 CFR 182.60; 582.60
CAS DataBase Reference 134-20-3(CAS DataBase Reference)
EWG's Food Scores 1
FDA UNII 981I0C1E5W
NIST Chemistry Reference Benzoic acid, 2-amino-, methyl ester(134-20-3)
Pesticides Freedom of Information Act (FOIA) Methyl anthranilate
EPA Substance Registry System Methyl anthranilate (134-20-3)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H319
Precautionary statements  P264-P280-P305+P351+P338-P337+P313
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36-37/39
WGK Germany  1
RTECS  CB3325000
21
Autoignition Temperature 986 °F
TSCA  Yes
HS Code  29224995
Hazardous Substances Data 134-20-3(Hazardous Substances Data)
Toxicity LD50 orally in rats, mice: 2910, 3900 mg/kg, P. M. Jenner et al., Food Cosmet. Toxicol. 2, 327 (1964)
NFPA 704
1
1 0

Methyl anthranilate price More Price(23)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich W268224 Methyl Anthranilate natural, ≥98%, FG 134-20-3 25g $108 2024-03-01 Buy
Sigma-Aldrich W268224 Methyl Anthranilate natural, ≥98%, FG 134-20-3 100g $323 2024-03-01 Buy
Sigma-Aldrich W268224 Methyl Anthranilate natural, ≥98%, FG 134-20-3 1kg $1830 2024-03-01 Buy
Sigma-Aldrich W268208 Methyl Anthranilate ≥98%, FCC, FG 134-20-3 sample-k $54.6 2024-03-01 Buy
Sigma-Aldrich W268208 Methyl Anthranilate ≥98%, FCC, FG 134-20-3 1kg $70.9 2024-03-01 Buy
Product number Packaging Price Buy
W268224 25g $108 Buy
W268224 100g $323 Buy
W268224 1kg $1830 Buy
W268208 sample-k $54.6 Buy
W268208 1kg $70.9 Buy

Methyl anthranilate Chemical Properties,Uses,Production

Description

Methyl anthranilate, also known as MA, methyl 2-amino benzoate or carbo methoxy aniline, is an ester of anthranilic acid. Its chemical formula is C8H9NO2.

Chemical Properties

Methyl anthranilate has a characteristic orange-flower odor and a slightly bitter, pungent taste. May be prepared by heating anthranilic acid and methyl alcohol in the presence of sulfuric acid and subsequent distillation.

Chemical Properties

Methyl Anthranilate occurs in a large number of blossom essential oils (e.g., neroli, ylang-ylang, and jasmine oils), grapes, and citrus oils. It occurs as white crystals (mp 24–25°C), or a yellowish liquid, that show blue fluorescence and have an orange blossom odor. Methyl anthranilate is prepared by esterification of anthranilic acid with methanol or by reaction of isatoic anhydride with methanol.
It is used in a large number of blossom fragrances. However, its use in perfumes for soaps and cosmetics is limited because it causes discoloration. It is used in flavor compositions (e.g., in grape and citrus flavors).

Occurrence

Methyl anthranilate naturally occurs in the Concord grapes and other Vitis labrusca grapes or hybrids thereof, and in bergamot, black locust, champaca , gardenia, jasmine, lemon, mandarin, neroli, oranges, rue oil, strawberry, tuberose, wisteria, galangal and ylang ylang. It is also a primary component of the essential apple flavor, along with ethyl acetate and ethyl butyrate.It is also secreted by the musk glands of foxes and dogs, and lends a "sickly sweetness" to the smell of rotting flesh.

Uses

Methyl anthranilate acts as a bird repellent. It is food-grade and can be used to protect corn, sunflowers, rice, fruit, and golf courses. Dimethyl anthranilate (DMA) has a similar effect. It is also used for the flavor of grape Kool Aid. It is used for flavoring of candy, soft drinks (e.g. grape soda), gums, and drugs.
Methyl anthranilate both as a component of various natural essential oils and as a synthesised aroma-chemical is used extensively in modern perfumery . It is also used to produce Schiff's Bases with aldehydes, many of which are also used in perfumery. In a perfumery context the most common Schiff's Base is known as aurantiol - produced by combining methyl anthranilate and hydroxyl citronellal.

Definition

ChEBI: Methyl anthranilate is a benzoate ester that is the methyl ester of anthranilic acid. It has a role as a metabolite and a flavouring agent. It derives from an anthranilic acid.

Preparation

By heating anthranilic acid and methyl alcohol in the presence of sulfuric acid and subsequent distillation.

Synthesis Reference(s)

Tetrahedron Letters, 33, p. 3599, 1992 DOI: 10.1016/S0040-4039(00)92512-7

General Description

Clear colorless to tan liquid with an odor of grapes. Has light blue fluorescence.

Air & Water Reactions

Methyl anthranilate is sensitive to air and light. Slightly water soluble .

Reactivity Profile

An amine and ester. Amines are chemical bases. They neutralize acids to form salts plus water. These acid-base reactions are exothermic. The amount of heat that is evolved per mole of amine in a neutralization is largely independent of the strength of the amine as a base. Amines may be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen is generated by amines in combination with strong reducing agents, such as hydrides. Esters react with acids to liberate heat along with alcohols and acids. Strong oxidizing acids may cause a vigorous reaction that is sufficiently exothermic to ignite the reaction products. Heat is also generated by the interaction of esters with caustic solutions. Flammable hydrogen is generated by mixing esters with alkali metals and hydrides.

Fire Hazard

Methyl anthranilate is combustible.

Toxicology

Methyl anthranilate is a colorless liquid that has a sweet, fruity, grape-like flavor. It is found in the essential oils of orange, lemon, and jasmine and has been widely used to create imitation Concord grape flavor. Table 10.8 shows the acute toxicity of methyl anthranilate. Methyl anthranilate promotes some allergic reactions on human skin, which has led to it being prohibited for use in cosmetic products.

Safety Profile

Moderately toxic by ingestion. Experimental reproductive effects. A skin irritant. See also ESTERS. Combustible liquid. When heated to decomposition it emits toxic fumes of NOx.

Safety

Methyl anthranilate is a plant-based compound with a long history of use as a flavor additive for foods and  beverages, and as an aromatic used extensively in perfumery. As such,  the US Department of Agriculture (USDA) and the Food and Drug  Administration (FDA) have approved MA as "generally recognized as safe".

Metabolism

It is probable that this ester is hydrolysed and the anthranilate is excreted mostly as oaminobenzoyl glucuronide (Charconnet-Harding, Dalgliesh & Neuberger, 1953).

Solubility in organics

Methyl anthranilate is soluble in ethanol and propylene glycol. It is insoluble in paraffin oil.

Toxicity evaluation

Even though MA is palatable to humans, it is an irritant to birds. The bird-repellent properties of MA and related compounds were discovered in the late 1950s (25). The mode of action is via the trigeminal nerve. Thus, all avian species tested so far perceive MA as an irritant, not as a taste repellent per se.

85-41-6
134-20-3
Synthesis of Methyl anthranilate from Phthalimide
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View Lastest Price from Methyl anthranilate manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Methyl anthranilate pictures 2024-12-20 Methyl anthranilate
134-20-3
US $6.00 / kg 1kg 99% 2000KG/Month HebeiShuoshengImportandExportco.,Ltd
Methyl anthranilate pictures 2024-12-20 Methyl anthranilate
134-20-3
US $2.00 / KG 1KG 99% 1000mt/year Jinan Finer Chemical Co., Ltd
Methyl Anthranilate pictures 2024-12-20 Methyl Anthranilate
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US $120.00 / kg 1kg 99% 20ton Hebei Zhuanglai Chemical Trading Co.,Ltd
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