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Methyl2-amino-3-nitrobenzoate

CAS 57113-91-4 · Amine · 2 functional traits · cGMP compliant · Ships from USA in 2-3 days

Amine

Methyl2-amino-3-nitrobenzoate

Esters PharmaceuticalPolymerAgrochemicalCatalysisFine ChemicalGreen Chemistry
CAS Number 57113-91-4
Category Amine · Ester
Origin USA
Compliance cGMP

Questions? Contact our chemistry team:

chemistry@chem-contract.com | +1 (714) 732-8549
In stock — typically ships within 2-3 business days

About Methyl2-amino-3-nitrobenzoate

Methyl2-amino-3-nitrobenzoate (CAS Number: 57113-91-4) is an amine-functionalized compound with nucleophilic nitrogen reactivity. ChemContract Research supplies this simple-complexity compound in high purity from our Huntington Beach, California facility, ensuring consistent quality and reliable domestic delivery throughout the United States.

Amines are among the most prevalent functional groups in drug molecules — over 80% of small-molecule pharmaceuticals contain at least one amine moiety. Ester hydrolysis by cellular esterases is the most commonly exploited prodrug activation mechanism — enabling drugs that cannot cross biological membranes as free acids.

Primary applications include buchwald–hartwig amination for aryl c–n bond construction and prodrug development to mask carboxylic acids and improve membrane permeability. This compound serves researchers and manufacturers across the pharmaceutical, polymer, agrochemical sectors. Whether you require Methyl2-amino-3-nitrobenzoate for early-stage research, process development, or commercial-scale production, ChemContract Research offers flexible ordering from milligram to multi-kilogram quantities with custom synthesis options and full batch documentation including Certificates of Analysis (CoA) and Safety Data Sheets.

Functional Groups: Amine (–NH₂/–NHR)Ester (–COOR)

Amine Applications & Target Industries

How Methyl2-amino-3-nitrobenzoate is used across pharmaceutical and polymer sectors

01

Buchwald–Hartwig amination for aryl C–N bond construction

02

Prodrug development to mask carboxylic acids and improve membrane permeability

03

Reductive amination with aldehydes and ketones for secondary amine synthesis

04

Protecting group for hydroxyl functionalities (acetate, benzoate)

05

Salt formation to improve drug solubility and bioavailability

06

Ring-opening polymerization monomer for biodegradable polymers

Target Industries: PharmaceuticalPolymerAgrochemicalCatalysisFine ChemicalGreen Chemistry

Methyl2-amino-3-nitrobenzoate Specifications

Detailed specifications for this amine, including purity, molecular weight, and analytical data are available upon request. Every batch from ChemContract Research includes:

  • Certificate of Analysis (CoA) with purity verification
  • HPLC, NMR, and/or mass spectrometry characterization data
  • Material Safety Data Sheet (MSDS/SDS)
  • Batch-specific documentation and lot traceability
  • Custom analytical testing available on request
Request Full Specifications

Quick Reference

Compound Name Methyl2-amino-3-nitrobenzoate
Type Amine
Category Amine · Ester
Purity ≥95% (custom grades available)
Complexity Simple (2 functional groups, 0 rings)
Compliance cGMP
Packaging mg to kg scale

Storage & Handling for Amines

Handling Guidelines

Amines may have strong odors and can be corrosive to skin. Handle under adequate ventilation with chemical-resistant gloves and eye protection. Some esters are volatile and flammable. Handle in a well-ventilated area. Keep away from ignition sources.

Storage Conditions

Store in a cool, well-ventilated area away from acids and oxidizing agents. Keep containers tightly sealed as many amines are hygroscopic. Store at room temperature in a tightly sealed container away from heat and open flame.

Why Buy Methyl2-amino-3-nitrobenzoate From ChemContract?

Quality Assured

Every batch of Methyl2-amino-3-nitrobenzoate is produced under cGMP conditions with full CoA documentation, HPLC purity verification, and lot traceability.

Fast USA Shipping

Ship from our Huntington Beach, CA facility with 2-3 business day domestic delivery. No import delays, no customs fees, no tariff surprises.

Custom Synthesis

Need a specific grade, quantity, or derivative of Methyl2-amino-3-nitrobenzoate? Our team of PhD chemists can develop custom synthesis solutions for your exact requirements.

Frequently Asked

Common questions about Methyl2-amino-3-nitrobenzoate

What is Methyl2-amino-3-nitrobenzoate used for? +

Methyl2-amino-3-nitrobenzoate is an amine-functionalized compound with nucleophilic nitrogen reactivity used primarily in the pharmaceutical and polymer industries. Key applications include buchwald–hartwig amination for aryl c–n bond construction and prodrug development to mask carboxylic acids and improve membrane permeability.

Where can I buy Methyl2-amino-3-nitrobenzoate in the USA? +

ChemContract Research is a trusted USA-based supplier of Methyl2-amino-3-nitrobenzoate. We offer competitive pricing, fast domestic shipping from our Huntington Beach, California facility, and full quality documentation including Certificates of Analysis (CoA). Request a quote at chemistry@chem-contract.com or call +1 (714) 732-8549.

What purity levels are available for Methyl2-amino-3-nitrobenzoate? +

ChemContract Research supplies Methyl2-amino-3-nitrobenzoate in multiple purity grades: ≥95% standard grade, ≥97% high-purity grade, and ≥99% ultra-high-purity grade depending on application requirements. We can also provide custom purity grades through our synthesis capabilities. Contact us for specific purity information and CoA documentation.

Can ChemContract synthesize Methyl2-amino-3-nitrobenzoate in custom quantities? +

Yes. ChemContract Research offers custom synthesis services for Methyl2-amino-3-nitrobenzoate from milligram to multi-kilogram scale. Our cGMP-compliant facilities and experienced chemists can accommodate custom specifications, packaging requirements, and delivery timelines. Contact our team to discuss your project.

What reactions can I perform with the amine group in Methyl2-amino-3-nitrobenzoate? +

The amine functionality in Methyl2-amino-3-nitrobenzoate enables diverse transformations: reductive amination with aldehydes/ketones, acylation to form amides, sulfonylation to form sulfonamides, Buchwald–Hartwig coupling with aryl halides, urea and carbamate formation, and salt generation for improved drug properties. The nucleophilicity of the nitrogen makes it one of the most versatile handles in synthetic chemistry.

How should I store Methyl2-amino-3-nitrobenzoate? +

Store in a cool, well-ventilated area away from acids and oxidizing agents. Keep containers tightly sealed as many amines are hygroscopic. Store at room temperature in a tightly sealed container away from heat and open flame. Always consult the compound-specific Safety Data Sheet (SDS) provided with your order for detailed storage requirements. ChemContract Research includes handling and storage documentation with every shipment.

What is the CAS number of Methyl2-amino-3-nitrobenzoate? +

The CAS Registry Number for Methyl2-amino-3-nitrobenzoate is 57113-91-4. This unique identifier is used worldwide to reference this specific compound in chemical databases, regulatory filings, and scientific literature. ChemContract Research supplies this compound with full quality documentation. Contact us at chemistry@chem-contract.com for availability and pricing.

Chemical analysis laboratory with HPLC instruments for purity and impurity testing Custom chemical synthesis reaction setup for pharmaceutical intermediate production

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