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trans-4-tert-Butoxycarbonylaminocyclohexanecarboxylic acid

CAS 130309-46-5 · Amine · 4 functional traits · cGMP compliant · Ships from USA in 2-3 days

Amine

trans-4-tert-Butoxycarbonylaminocyclohexanecarboxylic acid

Boc-Protected PharmaceuticalPolymerAgrochemicalCatalysisPeptide SynthesisFine Chemical
CAS Number 130309-46-5
Category Amine · Boc-Protected
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 trans-4-tert-Butoxycarbonylaminocyclohexanecarboxylic acid

trans-4-tert-Butoxycarbonylaminocyclohexanecarboxylic acid (CAS Number: 130309-46-5) is an amine-functionalized compound with nucleophilic nitrogen reactivity featuring a Cyclohexane ring with defined stereochemistry. ChemContract Research supplies this moderate-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. The Boc group is removed cleanly with TFA or HCl in dioxane, making it orthogonal to Fmoc, Cbz, and Alloc protecting groups — essential for synthesizing complex peptide therapeutics. Carboxylic acids are among the most synthetically versatile functional groups — they can be converted to amides, esters, acid chlorides, anhydrides, alcohols, and aldehydes in a single step.

Primary applications include buchwald–hartwig amination for aryl c–n bond construction and solid-phase peptide synthesis (spps) with orthogonal boc/fmoc strategies. This compound serves researchers and manufacturers across the pharmaceutical, polymer, agrochemical sectors. Whether you require trans-4-tert-Butoxycarbonylaminocyclohexanecarboxylic acid 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.

Ring Systems: Cyclohexane
Functional Groups: Amine (–NH₂/–NHR)Carboxylic acid (–COOH)Boc protecting group
Stereochemistry: Defined Configuration

Amine Applications & Target Industries

How trans-4-tert-Butoxycarbonylaminocyclohexanecarboxylic acid is used across pharmaceutical and polymer sectors

01

Buchwald–Hartwig amination for aryl C–N bond construction

02

Solid-phase peptide synthesis (SPPS) with orthogonal Boc/Fmoc strategies

03

Amide bond formation via EDC/HOBt or HATU coupling in peptide synthesis

04

Enantiopure building block for single-enantiomer drug development

05

Reductive amination with aldehydes and ketones for secondary amine synthesis

06

Multi-step pharmaceutical synthesis requiring selective amine deprotection

Target Industries: PharmaceuticalPolymerAgrochemicalCatalysisPeptide SynthesisFine Chemical

trans-4-tert-Butoxycarbonylaminocyclohexanecarboxylic acid 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 trans-4-tert-Butoxycarbonylaminocyclohexanecarboxylic acid
Type Amine
Category Amine · Boc-Protected
Purity ≥95% (custom grades available)
Stereochemistry Defined configuration (chiral HPLC verified)
Complexity Moderate (3 functional groups, 1 ring)
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. Boc-protected compounds are generally stable. TFA deprotection generates isobutylene gas — perform in a fume hood. Acids may be corrosive or irritating. Handle with chemical-resistant gloves and eye protection. Use a fume hood for volatile acids. Handle with standard precautions. Ensure proper labeling of stereochemical identity to prevent mix-ups.

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 sealed container. Stable under neutral and basic conditions; avoid strong acids during storage. Store at room temperature in a tightly sealed container. Protect from moisture and strong bases. Store under recommended conditions. Some chiral compounds may racemize at elevated temperatures or in the presence of base.

Why Buy trans-4-tert-Butoxycarbonylaminocyclohexanecarboxylic acid From ChemContract?

Quality Assured

Every batch of trans-4-tert-Butoxycarbonylaminocyclohexanecarboxylic acid 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 trans-4-tert-Butoxycarbonylaminocyclohexanecarboxylic acid? Our team of PhD chemists can develop custom synthesis solutions for your exact requirements.

Frequently Asked

Common questions about trans-4-tert-Butoxycarbonylaminocyclohexanecarboxylic acid

What is trans-4-tert-Butoxycarbonylaminocyclohexanecarboxylic acid used for? +

trans-4-tert-Butoxycarbonylaminocyclohexanecarboxylic acid 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 solid-phase peptide synthesis (spps) with orthogonal boc/fmoc strategies.

Where can I buy trans-4-tert-Butoxycarbonylaminocyclohexanecarboxylic acid in the USA? +

ChemContract Research is a trusted USA-based supplier of trans-4-tert-Butoxycarbonylaminocyclohexanecarboxylic acid. 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 trans-4-tert-Butoxycarbonylaminocyclohexanecarboxylic acid? +

ChemContract Research supplies trans-4-tert-Butoxycarbonylaminocyclohexanecarboxylic acid 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 trans-4-tert-Butoxycarbonylaminocyclohexanecarboxylic acid in custom quantities? +

Yes. ChemContract Research offers custom synthesis services for trans-4-tert-Butoxycarbonylaminocyclohexanecarboxylic acid 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 is the stereochemical purity of trans-4-tert-Butoxycarbonylaminocyclohexanecarboxylic acid? +

ChemContract Research supplies trans-4-tert-Butoxycarbonylaminocyclohexanecarboxylic acid with verified enantiomeric or diastereomeric purity as documented in our Certificate of Analysis (CoA). Chiral HPLC analysis is standard for stereodefined compounds. We can provide material with ≥98% ee/de for demanding applications. Contact us for specific optical purity requirements.

How do I remove the Boc group from trans-4-tert-Butoxycarbonylaminocyclohexanecarboxylic acid? +

The Boc protecting group in trans-4-tert-Butoxycarbonylaminocyclohexanecarboxylic acid is cleanly removed by treatment with trifluoroacetic acid (TFA, 20–50% in DCM) at room temperature, typically within 30–60 minutes. Alternative conditions include HCl in dioxane (4M) or trimethylsilyl triflate with 2,6-lutidine. The Boc group is stable to base, hydrogenation, and many nucleophilic conditions, making it orthogonal to Fmoc and Cbz groups.

How should I store trans-4-tert-Butoxycarbonylaminocyclohexanecarboxylic acid? +

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 sealed container. Stable under neutral and basic conditions; avoid strong acids during storage. Store at room temperature in a tightly sealed container. Protect from moisture and strong bases. Store under recommended conditions. Some chiral compounds may racemize at elevated temperatures or in the presence of base. 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 trans-4-tert-Butoxycarbonylaminocyclohexanecarboxylic acid? +

The CAS Registry Number for trans-4-tert-Butoxycarbonylaminocyclohexanecarboxylic acid is 130309-46-5. 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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