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アントラニル酸メチル

Methyl Anthranilate

HCID 8635
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基本情報概要名称と識別子物性安全と法規制化学と産業関連反応化合物ノート
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基本情報

CAS
134-20-3
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補完中

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
形式電荷
0
複雑度
147

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

TasteSlightly bitter, pungent
Food AdditivesFLAVORING AGENT OR ADJUVANT, SOLVENT OR VEHICLE -> FDA Substance added to food
Density · 4 件

1.1682 at 50 °F (NTP, 1992) - Denser than water; will sink

1.168 at 20 °C

Density: 1.1682 g/cu cm at 10 °C

1.161-1.169

Flavoring AgentsEU Flavoring substances
Color/Form

安全と法規制

安全情報は参考情報です。供給元の安全データシート(SDS)、適用法令、専門家による評価に代わるものではありません。

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]

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.

関連反応

269 件
反応記録を作成
HRID 2433 の反応式
HRID 2433反応物としてuspto-grants-1998_03
HRID 24734 の反応式
HRID 24734反応物としてuspto-grants-2005_02
HRID 53243 の反応式
HRID 53243反応物としてuspto-grants-1997_04
HRID 53258 の反応式
HRID 53258反応物としてuspto-grants-1997_04
HRID 76379 の反応式
HRID 76379反応物としてuspto-grants-2014_09
HRID 96982 の反応式
HRID 96982反応物としてTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
HRID 98308 の反応式
HRID 98308反応物としてTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
HRID 100921 の反応式
HRID 100921反応物としてTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
1 / 34 ページ

化合物ノート

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· 4 件

Crystals

Pale-yellow liquid with bluish fluorescence

Colorless to pale-yellow liquid or crystals with bluish fluorescence

Colorless to pale yellow liquid or solid

Solubility · 6 件

Slightly soluble (NTP, 1992)

In water, 2,850 mg/L at 25 °C

Slightly soluble in water

Very soluble in ethanol, ethyl ether

Freely soluble in alcohol or ether

Soluble in fixed oils, propylene glycol, volatile oils; slightly soluble in mineral oil; insoluble in glycerol

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
闪点
220 °F · 220 °F
貯蔵温度
Keep in dark place,Inert atmosphere,Room temperature
溶解性
アルコール: 易溶性(lit.)
外見
液体
酸解離定数(Pka)
1 · pK1:2.23(+1) (25°C)
色
クリアイエローブラウン
PH
7.5 · 7.5-8 (H2O, 20℃)Aqueous solution
臭い (Odor)
ブドウ臭
においのタイプ
フルーティーな
由来生物
synthetic
爆発限界(explosive limit)
1.4 · 1.4-7.8%(V)
水溶解度
わずかに溶ける
Merck
14 · 14,6020
JECFA Number
1534 · 1534
BRN
606965 · 606965
Henry's Law Constant
5.2 · 5.2×100 mol/(m3Pa) at 25℃, Duchowicz et al. (2020)
安定性
安定。可燃性。強力な酸化剤とは相容れない。
主な用途
フレーバーそして香料
化粧品成分の機能
香料
InChI
1S/C8H9NO2/c1-11-8(10)6-4-2-3-5-7(6)9/h2-5H,9H2,1H3
InChIKey
VAMXMNNIEUEQDV-UHFFFAOYSA-N
SMILES
COC(=O)c1ccccc1N
LogP
1.88 at · 1.88 at 20℃
表面張力
43.71 mN/m · 43.71 mN/m at 25°
CAS データベース
134 · 134-20-3(CAS DataBase Reference)
NISTの化学物質情報
2 · Benzoic acid, 2-amino-, methyl ester(134-20-3)
EPAの化学物質情報
Methyl anthranilate (134-20-3)
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).

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.

Reactive GroupEsters, Sulfate Esters, Phosphate Esters, Thiophosphate Esters, and Borate Esters
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.

Reactivity Profile · 1 件

An aromatic 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.

Air and Water ReactionsThis compound is sensitive to air and light. Slightly water soluble (NTP, 1992).
NFPA Hazard Classification · 3 件

1 - Materials that, under emergency conditions, can cause significant irritation.

1 - Materials that must be preheated before ignition can occur. Materials require considerable preheating, under all ambient temperature conditions, before ignition and combustion can occur.

0 - Materials that in themselves are normally stable, even under fire conditions.

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.

Disposal Methods · 2 件

SRP: Recycle any unused portion of the material for its approved use or return it to the manufacturer or supplier. Ultimate disposal of the chemical must consider: the material's impact on air quality; potential migration in air, soil or water; effects on animal, aquatic and plant life; and conformance with environmental and public health regulations. If it is possible or reasonable use an alternative chemical product with less inherent propensity for occupational harm/injury/toxicity or environmental contamination.

Product: Offer surplus and non-recyclable solutions to a licensed disposal company. Contact a licensed professional waste disposal service to dispose of this material. Contaminated packaging: Dispose of as unused product.

Preventive Measures · 5 件

Gloves must be inspected prior to use. Use proper glove removal technique (without touching glove's outer surface) to avoid skin contact with this product. Dispose of contaminated gloves after use in accordance with applicable laws and good laboratory practices. Wash and dry hands.

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.

Avoid contact with skin and eyes. Avoid inhalation of vapor or mist.

Handle in accordance with good industrial hygiene and safety practice. Wash hands before breaks and at the end of workday.

SRP: The scientific literature for the use of contact lenses by industrial workers is inconsistent. The benefits or detrimental effects of wearing contact lenses depend not only upon the substance, but also on factors including the form of the substance, characteristics and duration of the exposure, the uses of other eye protection equipment, and the hygiene of the lenses. However, there may be individual substances whose irritating or corrosive properties are such that the wearing of contact lenses would be harmful to the eye. In those specific cases, contact lenses should not be worn. In any event, the usual eye protection equipment should be worn even when contact lenses are in place.

Allowable TolerancesResidues 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.
Personal Protective Equipment (PPE) · 5 件

RECOMMENDED RESPIRATOR: Where the neat test chemical is weighed and diluted, wear a NIOSH-approved half face respirator equipped with an organic vapor/acid gas cartridge (specific for organic vapors, HCl, acid gas and SO2) with a dust/mist filter. (NTP, 1992)

Eye/face protection: Safety glasses with side-shields conforming to EN166. Use equipment for eye protection tested and approved under appropriate government standards such as NIOSH (US) or EN 166 (EU).

Skin protection: Handle with gloves.

Body Protection: Impervious clothing. The type of protective equipment must be selected according to the concentration and amount of the dangerous substance at the specific workplace.

Respiratory protection: Where risk assessment shows air-purifying respirators are appropriate use a full-face respirator with multipurpose combination (US) or type ABEK (EN 14387) respirator cartridges as a backup to engineering controls. If the respirator is the sole means of protection, use a full-face supplied air respirator. Use respirators and components tested and approved under appropriate government standards such as NIOSH (US) or CEN (EU).

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]
Ongoing Test Status · 2 件

The following link will take the user to the National Toxicology Program (NTP) Test Status of Agents Search page, which tabulates the results and current status of tests such as "Short-Term Toxicity Studies", "Long-term Carcinogenicity Studies", "Developmental Studies", "Genetic Toxicology Studies", etc., performed with this chemical. Testing status for methyl anthranilate is available.[Available from, as of February 1, 2019: https://ntpsearch.niehs.nih.gov/?e=True&ContentType=Testing+Status]

EPA has released the Interactive Chemical Safety for Sustainability (iCSS) Dashboard. The iCSS Dashboard provides an interactive tool to explore rapid, automated (or in vitro high-throughput) chemical screening data generated by the Toxicity Forecaster (ToxCast) project and the federal Toxicity Testing in the 21st century (Tox21) collaboration. /The title compound was tested by ToxCast and/or Tox21 assays/[USEPA; ICSS Dashboard Application; Available from, as of February 4, 2019: http://actor.epa.gov/dashboard/]

Soil Adsorption/Mobility · 1 件

The Koc of methyl anthranilate is estimated as 75(SRC), using a log Kow of 1.88(1) and a regression-derived equation(2). According to a classification scheme(3), this estimated Koc value suggests 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).

Natural Pollution Sources · 1 件

Methyl anthranilate is reported found in several essential oils: neroli, orange, bergamont, lemon, mandarin, jasmine, tuberose, gardenia, champaca, ylang-ylang and grape. It is also reported found in the juice and oil of Citris labrusca, peel oil of orange, bitter orange and tangerine, grapes, strawberry, cocoa, starfruit, tea, red and white wine, rice bran and babco fruit (Carica pentagona Heilborn)(1).

Atmospheric ConcentrationsSOURCE DOMINATED: Methyl anthranilate was detected not quantified in ambient air samples from the Thane Belapur Industrial area of Mumbai, India; sampling was conducted during summer, monsoon and winter seasons, 2004(1).
Human Toxicity Excerpts · 2 件

/HUMAN EXPOSURE STUDIES/ Maximization tests were carried out on groups of 24 and 26 volunteers. The material was tested at a 10% concentrationin petrolatum and produced no sensitization reactions.

/HUMAN EXPOSURE STUDIES/ Tested at 10% in petrolatum, it produced no irritation after a 48 hr closed-patch test on human subjects and this result was confirmed when the test was repeated.

Artificial Pollution Sources · 1 件

Methyl anthranilate's production and use as a flavor additive(1,2) may result in its release to the environment through various waste streams. Its use as a perfume(1,2) and bird repellant(3) will result in its direct release to the environment(SRC).

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
risk_code
36/37/38
化審法
(3)-1443
消防法
危-4-3-III
hazard_code
Xi
safety_code
26-36-37/39
自然発火温度
986 °F
Hazard Classifications
Eye Irrit. 2
ストレージクラス
10 - Combustible liquids
有毒物質データの
134-20-3(Hazardous Substances Data)

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.

Household ProductsInformation on 67 consumer products that contain Methyl anthranilate in the following categories is provided:
Use Classification · 6 件

Fragrance Ingredients

Flavouring Agent -> FLAVOURING_AGENT -> JECFA Functional Classes

Flavoring Agents -> JECFA Flavorings Index

Flavouring Agent -> FLAVOURING_AGENT -> JECFA Functional Classes

Flavouring Agent -> FLAVOURING_AGENT -> JECFA Functional Classes

Flavouring Agent -> FLAVOURING_AGENT -> JECFA Functional Classes

General Manufacturing Information · 3 件

All Other Chemical Product and Preparation Manufacturing

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

/Because it does not absorb UV radiation & has low molar absorptivity it is used as a sunscreen and ...in combination with other sunscreens or light-protectives. ... Dose: 5% in creams, lotions or ointments.

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.

上流・下流製品情報

上流原料

塩化すず(II)·2水和物安息香酸ナトリウムMethanol solution次亜塩素酸ナトリウムヨウ化カリウムジャスミン油落花生油ベンズアミドaminoformic acidぎ酸ナトリウム塩素酸ナトリウム安息香酸メチルビターオレンジ葉/小枝エキスアントラニル酸2-ニトロ安息香酸AminobenzoicAcid

下流製品

2-AMINO-3,5-DIBROMOBENZYL ALCOHOL3,5-ジブロモアントラニル酸メチルo-スルホベンズイミドナトリウム二水和物o-スルホベンズイミドN-メチルアントラニル酸 メチル2-アンモニオ-1,2-ベンゾイソチアゾール-3(2H)-オン1,1-ジオキシド2-[2-ヒドロキシ-3-[[(2,3-ジヒドロ-2-オキソ-1H-ベンゾイミダゾール)-5-イル]カルバモイル]-1-ナフチルアゾ]安息香酸メチルブロムヘキシン·塩酸塩ジチオりん酸O,O-ジエチルS-[(4-オキソ-1,2,3-ベンゾトリアジン-3(4H)-イル)メチル]サッカリンナトリウムN水和物3-イソプロピル-1H-2,1,3-ベンゾチアジアジン-4(3H)-オン2,2-ジオキシドPotassium saccharateアンブロキソール塩酸塩ビス[(2,3-ジヒドロ-1,2-ベンゾイソチアゾール1,1-ジオキシド)-2-イル]カルシウム2-(クロロスルホニル)安息香酸メチルビフェニル-2-カルボン酸メチル2,2'-イミノ二安息香酸

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.