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Anthranilic Acid

HCID 227
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Grundinformationen

CAS
118-92-3
Standard-SMILES
Nc1ccccc1C(=O)O
InChIKey
RWZYAGGXGHYGMB-UHFFFAOYSA-N
Summenformel
C7H7NO2
Durchschnittliche Molmasse
137,14 g/mol
Monoisotopische Masse
137,04767846

Überblick

Anthranilic acid appears as odorless white to pale-yellow or tan crystalline powder with a sweetish taste. (NTP, 1992)

Namen und Bezeichner

Bevorzugter Name
Anthranilic Acid
IUPAC
2-aminobenzoic acid
Englischer Name
Anthranilic acid
Summenformel
C7H7NO2
Molmasse
137.14

Namen und Synonyme

anthranilic acid2-aminobenzoic acid118-92-3o-aminobenzoic acidvitamin L1o-Carboxyaniline2-Carboxyanilineo-Anthranilic acidBenzoic acid, 2-amino-1-Amino-2-carboxybenzeneortho-Aminobenzoic acidBenzoic acid, o-amino-
Weitere Namen anzeigen
2-aaAnthranilic acid (VitaMin L1)2-AbzAntranilic acidanthranilicAnthranilic Acid 99 %
2-azaniumylbenzoateCarboxyanilineKyselina anthranilovaNCI-C01730Vitamin LKyselina o-aminobenzoova2-amino-Benzoic acidDTXSID8020094

Datenbank-Bezeichner

CAS
118-92-3、1321-11-5、98072-80-1
PubChem CID
227
DTXSID
DTXSID8020094
ChEMBL
CHEMBL14173
ChEBI
CHEBI:30754
UNII
0YS975XI6W
EC Number
204-287-5、308-537-5
Nikkaji
J2.912B

Eigenschaften

Berechnete StruktureigenschaftenWird ergänzt

XLogP
1,2
Polarare Oberfläche (TPSA)
63,3 Ų
H-Brücken-Donoren
2
H-Brücken-Akzeptoren
3
Frei drehbare Bindungen
1
Schwere Atome
10
Formalladung
0
Komplexität
136

Experimentelle und physikochemische Eigenschaften

Chemical Classes · 2 Einträge

Nitrogen Compounds -> Aminobenzoic Acids

Dye

Drugs · 2 Einträge

Pharmaceuticals -> Listed in ZINC15

Pharmaceuticals -> Synthetic Cannabinoids or Psychoactive Compounds

LogP · 3 Einträge

log Kow = 1.21

1.21

0.99-1.3

TasteSweetish taste
Density · 5 Einträge

1.412 (NTP, 1992) - Denser than water; will sink

1.412 at 20 °C

1.4 g/cm³

Relative density of the vapour/air-mixture at 20 °C (air = 1): 1.0

1.412 @ 20°C

Color/Form · 3 Einträge

White to pale yellow, crystalline powder

Leaves from alcohol

NEEDLE-LIKE CRYSTALS

Solubility · 6 Einträge

less than 0.1 mg/mL at 68 °F (NTP, 1992)

Freely soluble in alcohol, ether

Soluble in ethanol, ethyl ether, slightly soluble in trifluoroacetic acid, benzene, very soluble in chloroform, pyridine

Sicherheit und Regulatorisches

Sicherheitsangaben dienen nur zur Orientierung und ersetzen weder das Sicherheitsdatenblatt (SDB) des Lieferanten noch geltende Vorschriften oder eine fachliche Bewertung.

GHS-Klassifizierung

GHS Classification · 6 Einträge

This chemical does not meet GHS hazard criteria for 0.3% (1 of 321) of reports.

Danger

H318 (49.5%): Causes serious eye damage [Danger Serious eye damage/eye irritation]

P264+P265, P280, P305+P351+P338, P305+P354+P338, P317, and P337+P317 (click each P-code to see the statement)

Aggregated GHS information provided per 321 reports by companies from 9 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Danger

Gefahrenhinweise

Regulatory Information · 4 Einträge

Chemical: Benzoic acid, 2-amino-

List I Chemical: A chemical specified by regulation that, in addition to legitimate uses, is used in manufacturing a controlled substance in violation of the Act and is important to the manufacture of a controlled substance. (21 eCFR 1310.02)

Status: Active Update: 27-10-2021 https://echa.europa.eu/registration-dossier/-/registered-dossier/10130

Anthranilic acid: Does not have an individual approval but may be used under an appropriate group standard

Other Safety InformationIMAP assessments - Anthranilic acid and its calcium salt: Human health tier II assessment
Fire Hazards · 2 Einträge

This chemical is combustible. (NTP, 1992)

Combustible. Gives off irritating or toxic fumes (or gases) in a fire. Finely dispersed particles form explosive mixtures in air.

Fire PotentialCombustible. /from table/
Health Hazards · 1 Eintrag

SYMPTOMS: Symptoms of exposure to this compound may include nausea, vomiting, acidosis, rash, fever, methemoglobinemia and possibly hepatitis. Other symptoms of exposure include allergic reaction and cyanosis (bluing of skin). Skin contact may cause irritation, itching and dermatitis. It may also cause pruritus. Eye contact may cause irritation. Exposure may cause respiratory irritation, mucous membrane irritation, conjunctivitis and liver inflammation.

Chemie und Industrie

Pharmakologische Informationen

Metabolism/Metabolites · 6 Einträge

...Occurs as a metabolite of tryptophan, it is intermediate in biosynthesis of this amino acid in some microorganisms.

Formed from n-acetylanthranilic acid, anthranilamide, o-chloracetamidobenzoic acid, chorismic acid, n-formylanthranilic acid, n-hydroxyanthranilic acid, indole-3-acetic acid, isatic acid, isatin, methyl red, o-nitrobenzoic acid.

Yields anthranilic acid-n-beta-d-glucuronide in rat and rabbit; anthraniloyl-beta-d-glucuronic acid in rat and rabbit: Boyland E & Fahmy AR, Biochem J 91: 73 (1964). Arborine in Glycosmis; arborinine in Glycosmis: Groeger D & Johne S, Z Naturf, B 23: 1072 (1968) /from table/

Yields 1-(O-carboxyphenylamino)-1-deoxyribulose-5-phosphate in Neurospora; Wegman J & Demoss JA, J Biol Chem 240: 3781 (1965); in Aerobacter; Egan AF & Gibson F, Biochim Biophys Acta 130: 276 (1966); in Salmonella; Smith D & Bauerle RH, Biochemistry 8: 1451 (1969) /from table/

For more Metabolism/Metabolites (Complete) data for ANTHRANILIC ACID (9 total), please visit the HSDB record page.

Uremic toxins tend to accumulate in the blood either through dietary excess or through poor filtration by the kidneys. Most uremic toxins are metabolic waste products and are normally excreted in the urine or feces.

MeSH Pharmacological ClassificationDrugs used to prevent SEIZURES or reduce their severity.
Absorption, Distribution and Excretion · 2 Einträge

Less than 10% of dose (18 or 101 mg/kg bw)...given by ip injection was excreted in bile of rats...

... Anthranilic acids brain tissue concentrations in rat brain were significantly lower at birth as compared with those found prenatally; then ... increased in the first postnatal week and decreased thereafter.

Tissue LocationsEpidermis
Cellular LocationsCytoplasm
Metabolite PathwaysTryptophan metabolism

Verwendung und Herstellung

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In water, 3.5X10+3 mg/L at 25 °C

3.5 mg/mL

Solubility in water, g/100ml at 20 °C: 0.35 (poor)

Flash Point · 4 Einträge

340 °F (NTP, 1992)

150 °C

150 °C /from table/

150 °C

Boiling Point · 2 Einträge

Sublimes (NTP, 1992)

Sublimes

Decomposition200 °C
Melting Point · 4 Einträge

291 to 295 °F (NTP, 1992)

144-146 °C

146.5 °C

146-148 °C

Vapor Density · 2 Einträge

4.7 (calculated) (NTP, 1992) - Heavier than air; will sink (Relative to Air)

Relative vapor density (air = 1): 4.7

Physikochemische Eigenschaften

Schmelzpunkt
144 · 144-148 °C(lit.)
Siedepunkt
251.96 °C · 251.96°C (rough estimate)
Dichte
1.412 · 1.412
Dampfdichte
4.7 · 4.7 (vs air)
Dampfdruck
0.1 Pa · 0.1Pa at 52.6℃
Brechungsindex
1.5323 · 1.5323 (estimate)
Flammpunkt
150 °C · 150°C
storage temp.
0 °C · Store at 0°C
Löslichkeit
ethanol: may be clear to slightly hazy
pka
2.108 · 2.108(at 25℃)
Aggregatzustand
powder
Farbe
White to pale yellow crystalline
Wasserlöslichkeit
5.7 g/L · 5.7 g/L (25 ºC)
Merck
14 · 14,422
BRN
471803 · 471803
Henry's Law Constant
2.6 · 2.6×105 mol/(m3Pa) at 25℃, HSDB (2015)
Stabilität
Stable. Incompatible with strong oxidizing agents.
Major Application
bottom antireflective coatings, semiconductor devices, inks, hair dyes, cosmetics, treatment of chronic inflammatory diseases, depression
Kosmetik-Inhaltsstoffe Funktionen
SKIN CONDITIONING - MISCELLANEOUS
InChI
1S/C7H7NO2/c8-6-4-2-1-3-5(6)7(9)10/h1-4H,8H2,(H,9,10)
InChIKey
RWZYAGGXGHYGMB-UHFFFAOYSA-N
SMILES
Nc1c(cccc1)C(=O)O
LogP
0.99 at · 0.99 at 23℃ and pH3.7
CAS Datenbank
118 · 118-92-3(CAS DataBase Reference)
NIST chemische Informationen
Anthranilic acid(118-92-3)
EPA chemische Informationen
Anthranilic acid (118-92-3)
Hazards SummaryEmergency treatment: methemoglobinemia; [HSDB] Causes somnolence and ataxia in lethal-dose feeding studies of rats; [RTECS] An eye irritant; [ICSC] May cause irritation, methemoglobinemia, and liver injury; [CAMEO] An irritant; [MSDSonline]
FDA Requirements · 1 Eintrag

The following chemical has been specifically designated by the Administrator of the Drug Enforcement Administration as subject to the provisions of this part and parts 1309 and 1313 of this chapter. Anthranilic acid, its esters and its salts are List 1 chemicals; DEA Code: 8530.

Reactive GroupAcids, Carboxylic
Special ReportsDHEW/NCI; Bioassay of o-Anthranilic Acid for Possible Carcinogenicity (1978) Technical Rpt Series No. 36 DHEW Pub No. (NIH) 78-836
Reactivity ProfileANTHRANILIC ACID is incompatible with strong oxidizers. (NTP, 1992)
Atmospheric Standards · 1 Eintrag

This action promulgates standards of performance for equipment leaks of Volatile Organic Compounds (VOC) in the Synthetic Organic Chemical Manufacturing Industry (SOCMI). The intended effect of these standards is to require all newly constructed, modified, and reconstructed SOCMI process units to use the best demonstrated system of continuous emission reduction for equipment leaks of VOC, considering costs, non air quality health and environmental impact and energy requirements. Anthranilic acid is produced, as an intermediate or a final product, by process units covered under this subpart.

Chemical DangersOn combustion, forms nitrogen oxides. The solution in water is a weak acid. Reacts with oxidants. This generates fire hazard.

Sicherheit und Schutzausrüstung

Fire Fighting · 2 Einträge

Fires involving this material can be controlled with a dry chemical, carbon dioxide or Halon extinguisher. A water spray may also be used. (NTP, 1992)

Use powder, water spray, foam, carbon dioxide.

First Aid Measures · 4 Einträge

Fresh air, rest.

Rinse and then wash skin with water and soap.

First rinse with plenty of water for several minutes (remove contact lenses if easily possible), then refer for medical attention.

Rinse mouth. Give one or two glasses of water to drink. Seek medical attention if you feel unwell.

First Aid · 1 Eintrag

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.

Safe StorageSeparated from oxidants.
Fire Fighting ProceduresPowder, water spray, foam, carbon dioxide. /from table/
Storage ConditionsSeparated from strong oxidants. /from table/
Cleanup MethodsRemove all ignition sources. Sweep spilled substance into covered containers; if appropriate, moisten first to prevent dusting, then remove to safe place. Do NOT let this chemical enter the environment.
Nonfire Spill Response · 1 Eintrag

SMALL SPILLS AND LEAKAGE: Should a spill occur while you are handling this chemical, FIRST REMOVE ALL SOURCES OF IGNITION, then you should dampen the solid spill material with 60-70% ethanol and transfer the dampened material to a suitable container. Use absorbent paper dampened with 60-70% ethanol to pick up any remaining material. Seal the absorbent paper, and any of your clothes, which may be contaminated, in a vapor-tight plastic bag for eventual disposal. Solvent wash all contaminated surfaces with 60-70% ethanol followed by washing with a 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 · 1 Eintrag

SRP: The most favorable course of action is to use an alternative chemical product with less inherent propensity for occupational exposure or environmental contamination. 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 soil or water; effects on animal, aquatic, and plant life; and conformance with environmental and public health regulations.

Spillage Disposal · 1 Eintrag

Personal protection: particulate filter respirator adapted to the airborne concentration of the substance. Sweep spilled substance into covered containers. If appropriate, moisten first to prevent dusting. Then store and dispose of according to local regulations. Do NOT let this chemical enter the environment.

Preventive Measures · 2 Einträge

Local exhaust or breathing protection. Protective gloves. Safety goggles, or eye protection in combination with breathing protection if powder. Do not eat, drink, or smoke during work. /from table/

SRP: The scientific literature for the use of contact lenses in industry is conflicting. The benefit 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.

Eye PreventionWear safety spectacles.

Toxikologische Informationen

TreatmentKidney dialysis is usually needed to relieve the symptoms of uremic syndrome until normal kidney function can be restored.
Health EffectsChronic exposure to uremic toxins can lead to a number of conditions including renal damage, chronic kidney disease and cardiovascular disease.
Ecotoxicity Values · 2 Einträge

LC50 Leuciscus idus (freshwater fish; Ide) 215-1000 mg/L for 1 hr /conditions of bioassay not specified/

LC50 Leuciscus idus (Freshwater fish, Ide) 100-215 mg/L for 96 hr /conditions of bioassay not specified/

Environmental Fate · 3 Einträge

TERRESTRIAL FATE: Based on a classification scheme(1), an estimated Koc value of 110(SRC), determined from a log Kow of 1.21(2) and a regression-derived equation(3), indicates that anthranilic acid is expected to have high mobility in soil(SRC). The pKa of anthranilic acid is 2.14(4), indicating that this compound will primarily exist in anion form in the environment and anions generally do not adsorb more strongly to soils containing organic carbon and clay than their neutral counterparts(5). Volatilization of anthranilic acid from moist soil surfaces is not expected to be an important fate process(SRC) given an estimated Henry's Law constant of 3.8X10-11 atm-cu m/mole(SRC), using a fragment constant estimation method(6). Anthranilic acid is not expected to volatilize from dry soil surfaces(SRC) based upon an estimated vapor pressure of 2.8X10-4 mm Hg(SRC), determined from a fragment constant method(7). Anthranilic acid (10 ppm) degraded 100% in 2 days using a 1% suspension of Niagara silt loam at 25 °C(8).

AQUATIC FATE: Based on a classification scheme(1), an estimated Koc value of 110(SRC), determined from a log Kow of 1.21(2) and a regression-derived equation(3), indicates that anthranilic acid is not expected to adsorb to suspended solids and sediment(SRC). Volatilization from water surfaces is not expected(3) based upon an estimated Henry's Law constant of 3.8X10-11 atm-cu m/mole(SRC), developed using a fragment constant estimation method(4). According to a classification scheme(5), an estimated BCF of 3(SRC), from its log Kow(2) and a regression-derived equation(6), suggests the potential for bioconcentration in aquatic organisms is low(SRC). Anthranilic acid was shown to degrade rapidly in a variety of aqueous aerobic and anaerobic screening test(7-16). Anthranilic acid photodegrades rapidly in natural seawater(17). Anthranilic acid is shown to have a maximum absorption at 337 nm(18) and therefore may be susceptible to direct photolysis by sunlight(SRC).

ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), anthranilic acid, which has an estimated vapor pressure of 2.8X10-4 mm Hg at 25 °C(SRC), determined from a fragment constant method(2), is expected to exist solely as a vapor in the ambient atmosphere. Vapor-phase anthranilic acid 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 10 hours(SRC), calculated from its rate constant of 4.0X10-11 cu cm/molecule-sec at 25 °C(SRC) that was derived using a structure estimation method(3).

Adverse EffectsOccupational hepatotoxin - Secondary hepatotoxins: the potential for toxic effect in the occupational setting is based on cases of poisoning by human ingestion or animal experimentation.
Exposure Routes · 2 Einträge

The substance can be absorbed into the body by ingestion.

Endogenous, Ingestion, Dermal (contact)

Toxicity Summary · 1 Eintrag

Uremic toxins such as anthranilic acid are actively transported into the kidneys via organic ion transporters (especially OAT3). Increased levels of uremic toxins can stimulate the production of reactive oxygen species. This seems to be mediated by the direct binding or inhibition by uremic toxins of the enzyme NADPH oxidase (especially NOX4 which is abundant in the kidneys and heart) (A7868). Reactive oxygen species can induce several different DNA methyltransferases (DNMTs) which are involved in the silencing of a protein known as KLOTHO. KLOTHO has been identified as having important roles in anti-aging, mineral metabolism, and vitamin D metabolism. A number of studies have indicated that KLOTHO mRNA and protein levels are reduced during acute or chronic kidney diseases in response to high local levels of reactive oxygen species (A7869).

Signs and Symptoms · 2 Einträge

Redness. Pain.

As a uremic toxin, this compound can cause uremic syndrome. Uremic syndrome may affect any part of the body and can cause nausea, vomiting, loss of appetite, and weight loss. It can also cause changes in mental status, such as confusion, reduced awareness, agitation, psychosis, seizures, and coma. Abnormal bleeding, such as bleeding spontaneously or profusely from a very minor injury can also occur. Heart problems, such as an irregular heartbeat, inflammation in the sac that surrounds the heart (pericarditis), and increased pressure on the heart can be seen in patients with uremic syndrome. Shortness of breath from fluid buildup in the space between the lungs and the chest wall (pleural effusion) can also be present.

Ongoing Test Status · 1 Eintrag

The following link will take the user to the National Toxicology Program (NTP) Test Agent Search Results page, which tabulates all of the "Standard Toxicology & Carcinogenesis Studies", "Developmental Studies", and "Genetic Toxicity Studies" performed with this chemical. Clicking on the "Testing Status" link will take the user to the status (i.e., in review, in progress, in preparation, on test, completed, etc.) and results of all the studies that the NTP has done on this chemical. [http://ntp-apps.niehs.nih.gov/ntp_tox/index.cfm?fuseaction=ntpsearch.searchresults&searchterm=118-92-3]

Effluent ConcentrationsAnthranilic acid was detected in ammunition plant wastewater in Stadtallendorf, Germany(1).
ICSC Environmental DataThe substance is harmful to aquatic organisms. This substance may be hazardous to the environment. Special attention should be given to birds.
Soil Adsorption/Mobility · 1 Eintrag

The Koc of anthranilic acid is estimated as 110(SRC), using a log Kow of 1.21(1) and a regression-derived equation(2). According to a classification scheme(3), this estimated Koc value suggests that anthranilic acid is expected to have high mobility in soil. The pKa of anthranilic acid is 2.14(4), indicating that this compound will primarily exist in anion form in the environment and anions generally do not adsorb more strongly to soils containing organic carbon and clay than their neutral counterparts(5).

Regulatorische Informationen

FDA Requirements · 1 Eintrag

The following chemical has been specifically designated by the Administrator of the Drug Enforcement Administration as subject to the provisions of this part and parts 1309 and 1313 of this chapter. Anthranilic acid, its esters and its salts are List 1 chemicals; DEA Code: 8530.

Atmospheric Standards · 1 Eintrag

This action promulgates standards of performance for equipment leaks of Volatile Organic Compounds (VOC) in the Synthetic Organic Chemical Manufacturing Industry (SOCMI). The intended effect of these standards is to require all newly constructed, modified, and reconstructed SOCMI process units to use the best demonstrated system of continuous emission reduction for equipment leaks of VOC, considering costs, non air quality health and environmental impact and energy requirements. Anthranilic acid is produced, as an intermediate or a final product, by process units covered under this subpart.

Sicherheitsdaten

wgk
2
tsca
TSCA listed
hs_code
29224300
RTECS-Nr.
CB2450000
risk_code
36-37-36/37/38
hazard_code
Xi
safety_code
26-36-39
Speicherklasse
11 - Combustible Solids
Giftige Stoffe Daten
118-92-3(Hazardous Substances Data)
Hazard Classifications
Eye Dam. 1
Selbstentzündungstemperatur
>530°C
Uses · 6 Einträge

Used as an intermediate for dyes, drugs, pesticides, perfumes, flavors, and bird and insect repellents; Also used as a mold inhibitor in soya sauce and to enhance the milk production in cows; [HSDB]

Farming (Feed Additives) [Category: Industry]

Dyes, drugs, perfumes, and pharmaceuticals.

CHEM INT FOR CI ACID YELLOW 121, VAT VIOLET 13, VAT BLUE 1, CI DIRECT BROWN 112, MORDANT YELLOW, MORDANT RED 9, MORDANT BROWN 40, & PIGMENT RED 60, & FOR ITS ESTERS USED IN PERFUMES & FUNGICIDES, & IN SACCHARIN; CADMIUM SALT- AN ASCARICIDE IN SWINE; MOLD INHIBITOR IN SOYA SAUCE

As mold inhibitor in soya sauce; its esters have found applications in perfumes, synthetic flavors, bird and insect repellents, as fungicides for syrups

THERAP CAT (VET): The cadmium salt has been used as an acaricide in swine

U.S. Exports · 2 Einträge

(1972) No Data

(1975) No Data

U.S. Imports · 2 Einträge

(1972) 1.02X10+8 GRAMS (PRINCPL CUSTMS DISTS)

(1975) 5.00X10+6 GRAMS (PRINCPL CUSTMS DISTS)

U.S. Production · 3 Einträge

(1972) PROBABLY GREATER THAN 9.08X10+5 GRAMS

(1975) PROBABLY GREATER THAN 4.54X10+5 GRAMS

Production volumes for non-confidential chemicals reported under the Inventory Update Rule. [Table#3092]

Methods of Manufacturing · 4 Einträge

...PREPARED BY FISCHER IN 1896 BY HEATING 2-NITROSOBENZOIC ACID WITH AQ AMMONIUM SULFIDE @ 100 °C...PRODUCED COMMERCIALLY BY HOFMANN REACTION, IN WHICH PHTHALIMIDE IS REACTED WITH SODIUM HYPOCHLORITE & CAUSTIC SODA...

PREPD BY REDUCTION OF O-NITROBENZOIC ACID

TREATMENT OF PHTHALIMIDE WITH AN ALKALINE HYPOBROMITE SOLN.

2-Aminobenzoic acid is usually made from phthalic anhydride via sodium phthalamate. Oxidative decarboxylation (the Hofmann reaction) is carried out by the addition of sodium hypochlorite solution at 60 - 100 °C followed by acidification. The product is purified with activated carbon and bisulfite.

Formulations/PreparationsGRADES: TECHNICAL (95-98%); 99% OR BETTER.
DEA Listed Chemicals · 2 Einträge

Anthranilic acid, its esters, and its salts

A chemical specified by regulation that, in addition to legitimate uses, is used in manufacturing a controlled substance in violation of the Act and is important to the manufacture of a controlled substance. (21 eCFR 1310.02)

General Manufacturing Information · 2 Einträge

Benzoic acid, 2-amino-: ACTIVE

VITAMIN L & VITAMIN L1 FORMERLY USED TO DESCRIBE ANTHRANILIC ACID.

Anwendungen · 1 Eintrag

VerwendenAnthranilic acid can be used in organic synthesis to generate the benzyne intermediate. It is used as an intermediate for production of dyes, pigments, and saccharin. It and its esters are used in preparing perfumes to imitate jasmine and orange, pharmaceuticals and UV-absorber as well as corrosion inhibitors for metals and mold inhibitors in soya sauce.

Vor- und nachgelagerte Produkte

Vorgelagerte Rohstoffe

NatriumbenzoatNatriumhypochloritAmmoniak, wssrige LsungChlorWasserPhthalsureanhydridHydrogenchloridNatriumhydroxidHolzkohle, aktiviertSchwefelsure

Nachgelagerte Produkte

Tranilast2-Chlor-9-[3-(dimethylamino)propyl]thioxanthen-9-ol2-Carboxyphenylhydrazinium(1+)chloridBenzoesure, 2-[[1-Amino-7-[[4-[[6-amino-5-[(3-carboxy-4-hydroxyphenyl)azo]-1-hydroxy-3-sulfo-2-naphthalinyl]azo]-2-methoxyphenyl]azo]-8-hydroxy-3,6-disulfo-2-naphthalinyl]azo]-5-[[6-amino-5-[(3-carboxy-4-hydroxyphenyl)azo]-1-hydroxy-3-sulfo-2-naphthalinyl]azo]-6,10,12-Trichlornaphth[2,3-c]acridin-5,8,14(13H)-trion2-(4-Dimethylaminophenylazo)benzoesaeure2-IodbenzoesureLobenzaritEthylanthranilatPhenazine-1-carboxylic acid2,2'-DithiodibenzoesureTrinatrium-[μ-[2-[[1-hydroxy-6-[[[[5-hydroxy-6-[(2-hydroxy-5-sulfophenyl)azo]-7-sulfo-2-naphthyl]amino]carbonyl]amino]-3-sulfo-2-naphthyl]azo]benzoato(7-)]]dicuprat(3-)5-Iodoanthranilsaeure1,2-Dihydro-3H-indazol-3-on2-(3-oxobenzo[b]thien-2(3H)-yliden)benzo[b]thiophen-3(2H)-on4-Hydroxy-1-methyl-3-[(3-nitrophenyl)azo]-2-chinolonFluorescent Brightener Pf2-[(Phenylmethyl)amino]benzoesure2-Chlorthioxanthen-9-on2-Fluorbenzoesure2-(Dimethylamino)benzoesureN-Phenylanthranilsure2-AcetamidobenzoesureChinazolin-4(1H)-onBarium(2+)hydrogen-2-[(2-hydroxy-3,6-disulfonato-1-naphthyl)azo]benzoatPhenethylanthranilat3,5-Dibromobenzoic acid2-Amino-5-brombenzoesureN-(Carboxymethyl)anthranilsureAminoacridinClozapinReactive Blue X-R2,5-Dibrombenzoesure1-Benzyl-1,2-dihydro-3H-indazol-3-on2-(4-Chlorphenylthio)benzoesureKupfer, 2,2'-[Carbonylbis[imino(1-hydroxy-3-sulfo-6,2-naphthalindiyl)azo]]bis[benzoesure] Komplex1,3-Benzodithiolylium tetrafluoroborate6-Iodoquinazolin-4-one4H-3,1-Benzoxazin-2,4(1H)-dion4-Chloroquinazoline

Ergänzende Hinweise

DefinitionChEBI: An aminobenzoic acid that is benzoic acid having a single amino substituent located at position 2. It is a metabolite produced in L-tryptophan-kynurenine pathway in the central nervous system.