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Methyl anthranilate

CAS No.134-20-3
Chemical Name:Methyl anthranilate
Synonyms:NEROLI;FEMA 2682;Nevoli oil;2-AMinobenzoic;Methyl anthanilate;methyl anthranlate;METHYL ANTHRANILATE;Carbomethoxyaniline;Methyl anthranylate;Methylaminobenzoate
CBNumber:CB0722306
Molecular Formula:C8H9NO2
Formula Weight:151.16
MOL File:134-20-3.mol
Methyl anthranilate Property
mp : 24 °C(lit.)
bp : 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
Fp : 220 °F
storage temp. : -20°C Freezer
Water Solubility : slightly soluble
Sensitive : Air Sensitive
Merck : 14,6020
BRN : 606965
Stability:: Stable. Combustible. Incompatible with strong oxidizing agents.
CAS DataBase Reference: 134-20-3(CAS DataBase Reference)
NIST Chemistry Reference: Benzoic acid, 2-amino-, methyl ester(134-20-3)
EPA Substance Registry System: Benzoic acid, 2-amino-, methyl ester(134-20-3)
Safety
Hazard Codes : Xi
Risk Statements : 36/37/38
Safety Statements : 26-36-37/39
WGK Germany : 1
RTECS : CB3325000
F : 21
HS Code : 29224995
Hazardous Substances Data: 134-20-3(Hazardous Substances Data)

Methyl anthranilate Chemical Properties,Usage,Production

Chemical Properties
yellow to orange liquid with a smell of orange blossom
Usage
A useful synthetic intermediate.
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.
Methyl anthranilate Preparation Products And Raw materials
Raw materials
Stannous chloride dihydrate Sodium benzoate Sodium hypochlorite Potassium iodide JASMIN ABSOLUTE MOROCCO PEANUT OIL Benzamide aminoformic acid Sodium formate Sodium chlorate Methyl benzoate FEMA 2771 Anthranilic acid 2-Nitrobenzoic acid AminobenzoicAcid
Preparation Products
2-AMINO-3,5-DIBROMOBENZYL ALCOHOL Methyl 2-amino-3,5-dibromobenzoate Saccharin sodium dihydrate Saccharin Methyl 2-(methylamino)benzoate 1,2-benzisothiazol-3(2H)-one 1,1-dioxide, ammonium salt Pigment Red 175 Bromhexine hydrochloride AZINPHOS-ETHYL SACCHARIN SODIUM SALT DIHYDRATE Bentazone Potassium saccharate Ambroxol CALCIUM SACCHARIN Methyl 2-(chlorosulfonyl)benzoate
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134-20-3(Methyl anthranilate)Related Search:
Birch-Me Methyl propiolate Parathion-methyl Methyl hexadecanoate Pirimiphos-methyl METHYL STEARATE o-Anisidine 3-Nitrophthalic anhydride 4H-3,1-Benzoxazine-2,4(1H)-dione Methyl cinnamate Methylparaben 2-[[[[(4-Methoxy-6-methyl-1,3,5-triazin-2-yl)amino]carbonyl]amino]sulfonyl]benzoic acid methyl ester ETHYL ANTHRANILATE METHYL JASMONATE Anthranilic acid 4-Morpholineethanesulfonic acid Methyl 4-aminobenzoate Methyl anthranilate
NEROLI NEROLI OIL, ARTIFICIAL Organic Building Blocks Peptide Synthesis Specialty Synthesis Unnatural Amino Acid Derivatives Esters 2-AMINOBENZOIC ACID METHYL ESTER 134-20-3 C8 to C9 Aromatic Amino Acids Carbonyl Compounds Building Blocks ANTHRANILIC ACID METHYL ESTER ANTHRANILIC ACID:METHYL ESTER METHYL 2-ANTHRANILATE METHYL 2-AMINOBENZOATE METHYL O-AMINOBENZOATE METHYL ANTHRANILATE FEMA 2682 LABOTEST-BB LTBB000479 2-(Methoxycarbonyl)aniline 2-amino-benzoicacimethylester 2-Carbomethoxyaniline Benzoicacid,2-amino-,methylester Carbomethoxyaniline Methyl anthranylate Methyl ester of o-Aminobenzoic acid Methylaminobenzoate Methylester kyseliny anthranilove methylesterkyselinyanthranilove Neroli oil, artifical nerolioil,artifical Nevoli oil o-Amino methyl benzoate o-Aminobenzoic acid, methyl ester o-aminobenzoicacid,methylester o-aminobenzoicacidmethylester o-Carbomethoxyaniline Methl-O-Aminobenzoate ESTER Methyl anthanilate METHYL ANTHRANILATE, 99+% METHYL ANTHRANILATE 98+% FCC METHYL ANTHRANILATE, 100MG, NEAT METHYL ANTHRANILATE 99+% NATURAL MethylAnthranilateForSynthesis Benzoic acid, 2-amino-, methyl ester (9CI) ANTHRANILIC ACID METHYLESTER(SG) 2-AMINOBENZOICACIDMETHYLESTER(METHYLANTHRANILATE) H2NC6H4COOCH3 CARBOXYLICESTER Methyl anthranilate (o-Aminobenzoic acid methyl ester) Benzene derivatives 2-Aminobenzoesuremethylester METHYLANTHRANILAT (ANTHRANILSAEURE-METHYLESTER) METHYL ANTHRANILATE / METHYL 2-AMINOBENZOATE Aromatic Esters
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