1-(1-Adamantylcarbonyl) Proline

1-(1-Adamantylcarbonyl) Proline

Product name:1-(1-Adamantylcarbonyl) proline
Appearance: White Powder
CAS:35084-48-1
EINECS No:233-305-4
Molecular formula:C16H23NO3

Product Introduction
Product Name 1-(1-Adamantylcarbonyl) proline
Purity 98%
MF C16H23NO3
CAS 35084-48-1
Apperance White powder
Shelf life 2 years
Storage Cool and dry place

Products Description

 

1- (adamantane-1-carbonyl) -pyrr1- (1-Adamantylcarbonyl) Prolineolidine-2-carboxylic acid, also known as ACA, CAS number 35084-48-1, white or off-white powder, is a nitrogen-containing organic substance, used in supplement body.

product-352-199

 

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1- 1-Adamantylcarbonyl Proline Powder

 

Product COA

 

Certificate Of Analysis

 

Product Name

1-(1-Adamantylcarbonyl) proline

Cas. No.

35084-48-1

Batch No.

20230323

Packing

25kg/drum

Quantity

3500KG

Mfg. date

Mar.28,2024

Expiry date

Mar.27,2026

Analysis date

Mar.28,2024

Test Method

USP 43

Testing basis

Pharmacopoeia Standards

 

Testing items

Specifications

Test Results

Conclusion

Identification

It should meet the requirements fo

neomycin TLC identification test

It meets the requirements fo neomyein TLC identification test

Complies

To the xylene layer add the P- bromoaniline TS,and a vivid pink- red color should develop upon standing

It gives the positive reaction

A solution should respond to ths tests for Sulfate

It gives the positive reaction

PH

5.0-7.5

6.6

Complies

Loss on Drying

Not more than 8.0%

5.5

Complies

Assay

It has a poteney equivalent to not less than 600ug of neomyci pei mg. (calculated on the dried basis)

656μg/mg (calculated on the dried basis

618μg/mg(as is)

complies

Conclusion

Tested according to USP43 fit cofnplies with the requirement.

 

 

Pharmacological Efficacy of 1-(1-Adamantylcarbonyl) proline

 

1. Catalytic Applications in Organic Synthesis

Asymmetric Catalysis: Acts as a chiral organocatalyst in asymmetric reactions, such as:

Nucleophilic Addition Reactions: Catalyzes the asymmetric addition of aldehydes with alkyl azides, sulfonyl folates, and nitromethane, showing high activity towards alkyl azides.

Amination Reactions: Facilitates asymmetric amination processes, enabling the synthesis of chiral amines with stereoselectivity.

Aldol Reactions: Promotes the asymmetric aldol reaction between alcohols and aldehydes/ketones, yielding chiral aldol or hydroxyketone products.

2. Chiral Resolution and Synthetic Tool

Chiral Scaffold: Functions as a chiral resolving agent due to its inherent stereochemistry, aiding in the separation of enantiomers in organic synthesis.

Pharmaceutical Intermediate: Serves as a building block in the synthesis of complex organic molecules, particularly in pharmaceutical research where chiral purity is critical.

3. Physical and Chemical Properties Supporting Its Functions

Stability: Exhibits good stability under ambient conditions, allowing long-term storage without significant degradation.

Solubility: Shows low solubility in water but high solubility in organic solvents, making it suitable for organic reaction systems.

Structural Features: The adamantyl group enhances lipophilicity and steric hindrance, contributing to its catalytic selectivity, while the proline moiety provides the chiral center essential for asymmetric induction.

4. Limited Biomedical Efficacy

No proven therapeutic effects or biological activities (e.g., cognitive enhancement, memory improvement) are supported by peer-reviewed literature. Claims of neurological benefits in some commercial sources lack scientific validation.

 

Application of 1-(1-Adamantylcarbonyl) proline

Pharmacological Research: May act as a protease inhibitor, receptor modulator, or enzyme substrate due to the proline scaffold and adamantyl group.

Biomedical Studies: Could serve as a tool compound to investigate proline metabolism or protein-ligand interactions, though no specific biological activity has been documented.

Key Advantages

Rapid Onset & Short Duration: Mydriasis peaks within 20–30 minutes, with cycloplegia lasting 2–6 hours and residual dilation resolving within ~7 hours. This minimizes patient discomfort compared to longer-acting agents like atropine.

Good Ocular Penetration: Low dissociation constant enhances intraocular permeability, ensuring effective action at the iris and ciliary muscle.

Precautions

Contraindications: Angle-closure glaucoma (risk of acute intraocular pressure elevation) and hypersensitivity to anticholinergics.

Adverse Effects: Transient stinging, blurred vision, photophobia, and rarely, systemic effects (dry mouth, flushing) in pediatric patients.

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FAQ

 

Q: What's your MOQ ?

A: For the high value product, our MOQ starts from 1g and generally starts from 10gs. For other low, price product, our MOQ starts from 100g and 1kg.

Q: Is there a discount ?

A: Yes, for larger quantity, we always support with better price.

Q: How to confirm the Product Quality before placing orders ?

A: You can get free samples for some proucts, you only need to pay the shipping cost or arrange a courier to us and take the samples. You can send us your product specifications and requests, we will manufacture the products according to your requests.

Q: How to start orders or make payments ?

A: You can send our your Purchase order ( if your company has ), or just send a simple confirmation by email or by Trade Manager, and we will send you Proforma Invoice with our bank details for your confirmation, then you can make payment accordingly.

Q: How do you treat quality complaint ?

A: First of all, our quality control will reduce the quality problem to near zero. If there is a quality problem caused by us, we
will send you free goods for replacement or refund your loss.

 

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