アントラニル酸メチル

Methyl Anthranilate

HCID 8635CAS 134-20-3

基本情報

標準SMILES
COC(=O)c1ccccc1N
InChIKey
VAMXMNNIEUEQDV-UHFFFAOYSA-N
分子式
C8H9NO2
平均分子量
151.16 g/mol
単同位体質量
151.06332853

概要

Methyl anthranilate is a clear colorless to tan liquid with an odor of grapes. Has light blue fluorescence. (NTP, 1992)

名称と識別子

優先名称
Methyl Anthranilate
IUPAC
methyl 2-aminobenzoate
現地名
アントラニル酸メチル
英語名
Methyl anthranilate
分子式
C8H9NO2
分子量
151.16

名称と別名

METHYL ANTHRANILATEMethyl 2-aminobenzoate134-20-32-Aminobenzoic acid methyl esterMethyl o-aminobenzoateAnthranilic acid methyl estero-Carbomethoxyaniline2-Carbomethoxyaniline2-(Methoxycarbonyl)anilineBenzoic acid, 2-amino-, methyl esterFEMA No. 2682o-Aminobenzoic acid methyl ester
名称をさらに表示
アントラニル酸メチル2-アミノ安息香酸メチルメチルo-アミノベンゾアートメチルアントラニラートo-アミノ安息香酸メチルアンスラニル酸メチルメチル アントラnilエト2-(メトキシカルボニル)アニリンメチルアンスラニレートメチル 2-アミノベンゾアートO-ベンゾイル-N-メチルヒドロキシルアミンN-メチル-O-ベンゾイルヒドロキシルアミンメチルアミノ ベンゾアートMethyl antranilateNEROLINevoli oilFEMA 2682Methyl anthranylateMethylaminobenzoate
DTXSID6025567Methylester kyseliny anthraniloveCHEBI:73244981I0C1E5WNSC-3109DTXCID105567RefChem:157789205-132-4

データベース識別子

CAS
134-20-3
PubChem CID
8635
DTXSID
DTXSID6025567
ChEMBL
CHEMBL1493986
ChEBI
CHEBI:73244
UNII
981I0C1E5W
EC Number
205-132-4
Nikkaji
J2.018D

物性

構造計算による物性

XLogP
1.9
極性表面積
52.3 Ų
水素結合供与体数
1
水素結合受容体数
3
回転可能結合数
2
重原子数
11

実験および物理化学的性質

Chemical ClassesNitrogen Compounds -> Aminobenzoic Acids
CosmeticsMasking
FragrancesFragrance Ingredient (Methyl anthranilate) -> IFRA transparency List
Pesticides · 2 件

Other Treatment

Active substance -> EU Pesticides database: Pending

LogP · 3 件

log Kow = 1.88

1.88

1.88

Odor · 2 件

Grape-like odor

Orange blossom odor

物理化学的性質

融点
24 °C · 24 °C (lit.)
沸点
256 °C · 256 °C (lit.)
比重(密度)
1.168 g/mL · 1.168 g/mL at 25 °C (lit.)
蒸気圧
1 mm · 1 mm Hg ( 20 °C)
屈折率
20 · n20/D 1.582(lit.)
FEMA
2682 · 2682 | METHYL ANTHRANILATE
化学的性質 · 1 件

化学的特性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).

安全と法規制

GHS分類

GHS Classification · 6 件

This chemical does not meet GHS hazard criteria for 0.2% (4 of 2660) of reports.

Warning

H319 (99.8%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]

P264+P265, P280, P305+P351+P338, and P337+P317 (click each P-code to see the statement)

Aggregated GHS information provided per 2660 reports by companies from 13 notifications to the ECHA C&L Inventory.

Warning

危険有害性情報

Regulatory Information · 5 件

Chemical: Benzoic acid, 2-amino-, methyl ester

Commission Regulation (EC) No 1565/2000 (Repealed by Com. Implementing Reg. (EU) No 872/2012)

Benzoic acid, 2-amino-, methyl ester is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of Benzoic acid, 2-amino-, methyl ester are required to report information about their production and use of this chemical to the EPA under the Toxic Substances Control Act (TSCA). (40 eCFR Part 711)

Status: Active Update: 24-02-2021 https://echa.europa.eu/registration-dossier/-/registered-dossier/19558

Benzoic acid, 2-amino-, methyl ester: Does not have an individual approval but may be used under an appropriate group standard

Other Safety InformationIMAP assessments - Benzoic acid, 2-amino-, methyl ester: Human health tier I assessment
Fire HazardsThis chemical is combustible. (NTP, 1992)
Fire PotentialCombustible liquid.
Health HazardsSYMPTOMS: This compound is an irritant to the skin.
Hazards Summary · 1 件

A mutagen, reproductive effector, and moderate skin irritant; Causes somnolence and coma in lethal-dose feeding studies of rats; [RTECS] Safe to use as a flavoring agent in food; ADI = 0-1.5 mg/kg; [JECFA] A skin irritant; [CAMEO] A skin and eye irritant; [eChemPortal: ERMA] Included in list of fragrance substances with negative human data, i.e. patch tests of patients with suspected contact allergy to fragrance ingredients which yielded negative results.; [EC: Scientific Committee on Consumer Safety: Fragrance allergens in cosmetic products (2011)] An irritant; [MSDSonline]

安全と保護具

Fire Fighting · 1 件

This compound is not very flammable but any fire involving this compound may produce dangerous vapors. You should evacuate the area. All firefighters should wear full-body protective clothing and use self-contained breathing apparatuses. You should extinguish any fires involving this chemical with a dry chemical, carbon dioxide, foam, or halon extinguisher. (NTP, 1992)

First Aid · 1 件

EYES: First check the victim for contact lenses and remove if present. Flush victim's eyes with water or normal saline solution for 20 to 30 minutes while simultaneously calling a hospital or poison control center. Do not put any ointments, oils, or medication in the victim's eyes without specific instructions from a physician. IMMEDIATELY transport the victim after flushing eyes to a hospital even if no symptoms (such as redness or irritation) develop.

Fire Fighting Procedures · 2 件

Suitable extinguishing media: Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide. Advice for firefighters: Wear self-contained breathing apparatus for firefighting if necessary.

Water or foam may cause frothing. /Use/ alcohol foam.

Storage ConditionsKeep container tightly closed in a dry and well-ventilated place. Storage class (TRGS 510): 10: Combustible liquids.
Cleanup Methods · 1 件

ACCIDENTAL RELEASE MEASURES: Personal precautions, protective equipment and emergency procedures: Use personal protective equipment. Avoid breathing vapors, mist or gas. Ensure adequate ventilation. Environmental precautions: Do not let product enter drains. Methods and materials for containment and cleaning up: Soak up with inert absorbent material and dispose of as hazardous waste. Keep in suitable, closed containers for disposal.

Nonfire Spill Response · 1 件

SMALL SPILLS AND LEAKAGE: If you spill this chemical, use absorbent paper to pick up all liquid spill material. Your contaminated clothing and absorbent paper should be sealed in a vapor-tight plastic bag for eventual disposal. Solvent wash all contaminated surfaces with alcohol followed by washing with a strong soap and water solution. Do not reenter the contaminated area until the Safety Officer (or other responsible person) has verified that the area has been properly cleaned.

毒性情報

Ecotoxicity Values · 5 件

LC50; Species: Ictalurus punctatus (Channel catfish) fry; Conditions: static; Concentration: 20.08 mg/L for 24 hr (95% confidence interval: 12.77-30.35 mg/L)

LC50; Species: Ictalurus punctatus (Channel catfish) fry; Conditions: static; Concentration: 17.35 mg/L for 48 hr (95% confidence interval: 12.17-24.4 mg/L)

LC50; Species: Ictalurus punctatus (Channel catfish) fry; Conditions: static; Concentration: 16.94 mg/L for 72 hr (95% confidence interval: 11.88-23.95 mg/L)

LC50; Species: Ictalurus punctatus (Channel catfish) fry; Conditions: static; Concentration: 16.23 mg/L for 96 hr (95% confidence interval: 11.57-22.47 mg/L)

For more Ecotoxicity Values (Complete) data for Methyl anthranilate (18 total), please visit the HSDB record page.

Environmental Fate · 3 件

TERRESTRIAL FATE: Based on a classification scheme(1), an estimated Koc value of 75(SRC), determined from a log Kow of 1.88(2) and a regression-derived equation(3), indicates that methyl anthranilate is expected to have high mobility in soil(SRC). However, aromatic amines are expected to bind strongly to humus or organic matter in soils due to the high reactivity of the aromatic amino group(4,5), suggesting that mobility may be much lower in some soils(SRC). Volatilization of methyl anthranilate from moist soil surfaces is expected to be an important fate process(SRC) given an estimated Henry's Law constant of 1.9X10-6 atm-cu m/mole(SRC), derived from its vapor pressure, 2.7X10-2 mm Hg(6), and water solubility, 2,850 mg/L(7). Methyl anthranilate is not expected to volatilize from dry soil surfaces(SRC) based upon its vapor pressure(6). Utilizing a soil biodegradation screening test, 100% biodegradation in 64 days of analogous 2-aminobenzoic acid(8) indicates that biodegradation of methyl anthranilate may be an important environmental fate process in soil(SRC).

AQUATIC FATE: Based on a classification scheme(1), an estimated Koc value of 75(SRC), determined from a log Kow of 1.88(2) and a regression-derived equation(3), indicates that methyl anthranilate is not expected to adsorb to suspended solids and sediment(SRC). Volatilization from water surfaces is expected(4) based upon an estimated Henry's Law constant of 1.9X10-6 atm-cu m/mole(SRC), derived from its vapor pressure, 2.7X10-2 mm Hg(5), and water solubility, 2,850 mg/L(6). Using this Henry's Law constant and an estimation method(4), volatilization half-lives for a model river and model lake are 24 and 180 days, respectively(SRC). According to a classification scheme(7), an estimated BCF of 8(SRC), from its log Kow(2) and a regression-derived equation(3), suggests the potential for bioconcentration in aquatic organisms is low(SRC). Methyl anthranilate, present at 50 mg/L, exhibited 100% biodegradation in 20 days when incubated in dechlorinated, charcoal-filtered water(8) indicating that biodegradation of methyl anthranilate may be an important environmental fate process in water(SRC).

ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), methyl anthranilate, which has a vapor pressure of 2.7X10-2 mm Hg at 25 °C(2), is expected to exist solely as a vapor in the ambient atmosphere. Vapor-phase methyl anthranilate is degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals(SRC); the half-life for this reaction in air is estimated to be 11 hrs(SRC), calculated from its rate constant of 3.5X10-11 cu cm/molecule-sec at 25 °C(SRC) that was derived using a structure estimation method(3). Methyl anthranilate contains chromophores that absorb at wavelengths >290 nm(4) and, therefore, may be susceptible to direct photolysis by sunlight(SRC).

Adverse EffectsNeurotoxin - Other CNS neurotoxin
Toxicity Summary · 1 件

IDENTIFICATION AND USE: Methyl anthranilate can occur a colorless to pale-yellow liquid, or crystals with bluish fluorescence. It is used as a non-toxic and non-lethal bird repellent. It is used also in flavorings and perfumes. Although methyl anthranilate was not 100% effective in preventing honey bee stinging, it seemed to reduce number of stings below the average human LD50, indicative of a promising tool for preventing honey bee venom toxicity and wasp colonization. HUMAN STUDIES: Maximization tests were carried out on groups of 24 and 26 volunteers. The material was tested at a 10% concentration in petrolatum and produced no sensitization reactions. It produced no irritation after a 48 hr closed-patch test on human subjects and this result was confirmed when the test was repeated. ANIMAL STUDIES: Methyl anthranilate applied full strength to intact or abraded rabbit skin for 24 hr under occlusion was moderately irritating. Groups of 10 male and 10 female weanling rats were maintained for a period of 115 days on diets containing methyl anthranilate at levels of 0, 3,000 and 10,000 ppm. The only observable effects noted at the 10,000 ppm level were increases in the average weights of the liver and kidneys, and slight (minimal) histological changes in the kidneys. There was no increase in the incidence of primary lung tumors in mice over a period of 24 weeks, that received a total dose of methyl anthranilate of 2.25 or 11.2 g/kg bw (repeated ip injections three times a week for a total of 24 injections). Methyl anthranilate was found to be negative when tested for mutagenicity using the Salmonella/ microsome preincubation assay, Methyl anthranilate was tested in as many as 5 Salmonella typhimurium strains (TA1535, TA1537, TA97, TA98, and TA100) in the presence and absence of metabolic activation. ECOTOXICITY STUDIES: No treatment-related mortality of catfish was observed. Handling times of catfish fingerlings captured by herons from tubs treated with methyl anthranilate-based bird repellent increased at application rates of 19.6 kg/ha or greater.

Ecotoxicity Excerpts · 2 件

/AQUATIC SPECIES/ ...The acute toxicity of methyl anthranilate /was tested/ in a static system against the fry of four species of fish. The LC50 at 24 hr for Atlantic salmon (Salmo salar L.) was 32.3 mg/L, with the no observable effect limit at 6 mg/L.

/AQUATIC SPECIES/ ...The methyl anthranilate-based bird repellent, ReJeX-iT TP-40TM (TP-40), /was evaluated/ for 1) its toxicity to channel catfish fingerlings (catfish), Ictalurus punctatus; 2) its effect on great blue heron (heron), Ardea herodias feeding behavior; 3) its efficacy in reducing heron predation on catfish; and 4) its effects on catfish growth. TP-40 effectively maintained MA /methyl anthranilate/ concentrations near the water's surface and below toxic levels for catfish in the water column. Water samples collected from 0.03 and 0.35 m below the surface of catfish rearing tanks (6,664 L) treated at application rates up to the equivalent of 200 kg/ha contained less than 5 ppm active ingredient, which is less than the no observable effect limit for catfish fry. No treatment-related mortality of catfish was observed. Handling times of catfish fingerlings captured by herons from tubs treated with TP-40 initially increased at application rates of 19.6 kg/ha or greater.

Plant ConcentrationsMethyl anthranilate occurrence in plants(1).[Table#2675]

法規制情報

FDA Requirements · 3 件

Synthetic flavoring substances and adjuvants /for animal drugs, feeds, and related products/ that are generally recognized as safe for their intended use, within the meaning of section 409 of the Act. Methyl anthranilate is included on this list.

Synthetic flavoring substances and adjuvants /for human consumption/ that are generally recognized as safe for their intended use, withn the meaning of section 409 of the Act. Methyl anthranilate is included on this list.

Sunscreen active ingredients. The active ingredient of the product consists of any of the following, within the concentration specified for each ingredient, and the finished product provides a minimum SPF value of not less than 2 as measured by the testing procedures established in subpart D of this part: ... (h) Methyl anthranilate up to 5 percent.

FIFRA Requirements · 2 件

New Active Ingredients ... includes pesticide active ingredients initially registered after November 1, 1984, that currently have active product registrations. By law, these newer pesticides are not subject to the reregistration program. They must, however, meet the new safety standard of the FQPA, and will be reviewed on a 15-year cycle under the registration review program. ... Active Ingredient Number: 128725; Type of Pesticide: biological - bird repellant; Use Site: food use, industrial, turf, commercial use; Year: 1995.

Residues of methyl anthranilate, a biochemical pesticide, are exempt from the requirement of a tolerance in or on all food commodities, when used in accordance with good agricultural practices.

安全データ

F
21
wgk
1
tsca
TSCA listed
rtecs
CB3325000
毒性
LD50 orally in rats, mice: 2910, 3900 mg/kg, P. M. Jenner et al., Food Cosmet. Toxicol. 2, 327 (1964)
hs_code
29224995

化学と産業

薬理情報

Metabolism/Metabolites · 1 件

Substantial evidence has accumulated showing that many esters readily undergo enzymatic hydrolysis into their component alcohols and acids. In the case of methyl anthranilate, there is direct experimental evidence showing that this ester, while only slowly hydrolyzed by artificial gastric or pancreatic juice, was readily hydrolyzed in rat liver homogenate (50% in 26.6 minutes) and rapidly hydrolyzed in a homogenate of rat small intestine mucosa (50% in 2.5 minutes). Methyl anthranilate has also been shown to be completely hydrolyzed (>99% in two hours) in pig liver homogenate; but was more resistant to hydrolysis in pig jejunum homogenate and completely unhydrolysed by a pancreatin preparation. The hydrolysis products of methyl anthranilate are, of course, methyl alcohol and anthranilic acid. Methyl alcohol is readily metabolized via well-known pathways to carbon dioxide and water. Anthranilic acid is a normal metabolite in man and is excreted in the urine, primarily, as o-aminohippuric acid and to a lesser extent as anthranilic acid glucuronide.

Cellular LocationsCytoplasm

用途と製造

Uses · 6 件

Found in neroli, ylang-ylang, bergamot, other essential oils, and grape juice; [Merck Index] Used to make perfumes and flavors; Effectively tested as a non-toxic and non-lethal bird repellent; Can also be added to liquids to protect migratory birds from contaminated standing water; Registered with the EPA for use in the US; [HSDB]

For methyl anthranilate (USEPA/OPP Pesticide Code: 128725) ACTIVE products with label matches. /SRP: Registered for use in the U.S. but approved pesticide uses may change periodically and so federal, state and local authorities must be consulted for currently approved uses./

Reported uses (ppm):

As perfume for ointments; manufacture of synthetic perfumes.

Flavoring, perfume (cosmetics and pomades).

For more Uses (Complete) data for Methyl anthranilate (8 total), please visit the HSDB record page.

U.S. Production · 3 件

2023: 8,500,000 - <10,000,000 lb

In public use before 1920. Use in fragnances in the USA amounts to about 50,000 lb/yr.

Non-confidential 2016 Chemical Data Reporting (CDR) information on the production and use of chemicals manufactured or imported into the United States. Chemical: Methyl anthranilate:

Consumer UsesFragrance
Industry UsesFragrance
Methods of Manufacturing · 3 件

Occurs in neroli, ylang-ylang, bergamot, jasmine, other essential oils and in grape juice; also obtained synthetically by esterifying anthranilic acid with CH3OH in presence of HCl.

Methyl anthranilate is prepared by esterification of anthranilic acid with methanol or by reaction of isatoic anhydride with methanol. Flavors and Fragrances, 3. Aromatic and Heterocyclic Compounds Johannes Panten Horst Surburg 28 January 2016

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

Formulations/Preparations · 5 件

Grade: Technical, FCC.

Rejex-it TP-40 (Avian Enterprises Limited LLC): Active ingredient: methyl anthranilate 40.0%.

Rejex-it MA (Avian Enterprises Limited LLC): Active ingredient: methyl anthranilate 98.5%.

Rejex-it AG-36 (Avian Enterprises Limited LLC): Active ingredient: methyl anthranilate 14.5%.

For more Formulations/Preparations (Complete) data for Methyl anthranilate (13 total), please visit the HSDB record page.

応用分野 · 5 件

用途有機合成原料。

説明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.

天然物の起源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.

使用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.

一般的な説明Clear colorless to tan liquid with an odor of grapes. Has light blue fluorescence.

調製方法

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

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補足説明

定義本品は、2-アミノ安息香酸とメタノールのエステルであり、次の化学式で表される。

定義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.

関連反応

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