Efrotomycin

Efrotomycin (CAS registry number 56592-32-6) is supplied as a chemical raw material for formulation and synthesis work. The molecular formula is C59H88N2O20, giving a molecular weight of 1145.3 g/mol. This is a polyfunctional organic compound of 59 carbon with 22 heteroatoms, predominantly aliphatic; of high molecular weight. Documents are issued per shipment rather than per catalogue entry: each batch is accompanied by a Certificate of Analysis, and safety data sheets, technical datasheets and third-party test reports are supplied on request for export documentation.

Product Overview

Applications

Pharmaceutical Intermediates &amp；APIs

Recorded applications for this entry: Pharmaceutical Intermediates &amp, APIs. Where your formulation differs, the relevant point to check is not the use category but the impurity profile — tell us the end use and we will map it to the specification.

For export enquiries, include the destination country and the intended application in your message. This lets us confirm whether the grade needs any additional documentation beyond the standard per-batch COA, and whether the packing suits the planned transport mode.

Packaging & Storage

Packing is per order / batch confirmation (not published) and purity is per batch COA (not published). Both are agreed at order stage; for export movements the packing is chosen with the transport mode and destination in mind, and drum, bag or repacked formats are all available. Storage: sealed, in a cool and dry place, away from direct sunlight.

Each shipment is accompanied by a batch Certificate of Analysis. For cross-border orders, MSDS, technical datasheets and third-party test reports can be issued to match your documentation set; declare the destination country when you enquire so the paperwork matches on arrival. Contact: info@591daili.com · +86-18553102138.

Quality & Documentation

COA (Certificate of Analysis) is provided with every batch. MSDS/technical data sheets and third-party test reports are available on request. Purity and packaging are subject to batch COA and order confirmation.

Molecular Character — Selection Notes

What the structure means for your process

For this product specifically: the saturated aliphatic backbone is stable at ambient conditions, so oxidation risk comes mainly from oxygen, peroxides or trace transition metals introduced in processing rather than from the skeleton itself. If oxidisable components are also present, evaluate the order of addition during storage.

From a process-selection standpoint, This product is an aliphatic organic carrying 20 oxygen, 2 nitrogen, and is strongly lipophilic, essentially insoluble in water. defines where this material fits and where it does not. Three points deserve checking before purchase: structural type, which sets the reactive sites and compatibility; polarity class, which dictates the solvent system; and molecular-weight range, which governs dosage and dispersion feasibility.

How it behaves in your formulation

Above 500 g/mol this sits in the high-molecular-weight range, present as micelles, polymer solution or dispersed phase rather than dissolved molecules, so its function is structural. Confirm degree of shear thinning and batch-to-batch molecular-weight consistency, since both determine whether your finished product stays consistent.

Strongly lipophilic and effectively insoluble in water, so it serves as an oil-phase component: solvent carrier, thickener base or film former. Introducing it into an aqueous phase requires pre-dissolution in a small amount of solvent or an emulsified envelope; adding it dry will leave it floating.

Storage, handling and documents

On documentation: the batch COA travels with every shipment; MSDS, technical datasheets and third-party test reports can be issued on request. If your quality system requires supplier qualification documents — business licence, production permit, management-system certificates — state the destination country and the document list when you enquire, and we will assemble the set at once.

A few points on receipt and storage. control dust and wear eye protection, as the material can irritate mucous membranes; pre-disperse high-molecular-weight material, as adding it dry into a viscous medium clumps; pre-dissolve lipophilic material in a compatible solvent before introducing it to the aqueous phase; specific handling and PPE follow the MSDS issued with the batch.. For inbound or outbound shipments, confirm packing group and transport classification in advance to avoid demurrage caused by documentation mismatch.

Technical Profile

What this product is

Efrotomycin is a pharmaceutical intermediate or API compound with CAS registry number 56592-32-6 and molecular formula C59H88N2O20 (molecular weight 1145.3), belonging to the pharmaceutical intermediates and APIs segment of chemical raw materials.

This entry belongs to the pharmaceutical intermediates and APIs range, where the material is normally supplied against a stated grade rather than blended to a formula. Where a buyer works to a published standard, the useful conversation is about which data the grade is qualified against and how deviations are handled, rather than about the use category itself.

Efrotomycin is typically applied in Pharmaceutical Intermediates &amp, APIs.

Jinan Shenghe Chemical Co., Ltd. supplies Efrotomycin with stable inventory and provides a Certificate of Analysis (COA) with each batch; custom repacking is available per process requirement.

Identification

CAS number: 56592-32-6 — searchable in PubChem for physicochemical, safety and regulatory data.

Its molecular formula C59H88N2O20 comprises 59 C, 88 H, 2 N, 20 O atoms.

Also known as: Efrotomycin

Category: pharmaceutical intermediates and APIs

Applications and qualification

Within the pharmaceutical intermediates and APIs segment, the technical questions differ from other categories. Buyers here are usually working to a specification or a standard rather than to a general description, so the useful conversation covers impurity profile, particle size or assay method, and which data the grade is qualified against.

Application terms recorded for this entry: Pharmaceutical Intermediates &amp, APIs. If your specification differs, the point to check is not the use category but the impurity limits — send us the standard you work to and we will confirm what can be supplied against it.

For qualification work, we can supply a sample batch with full documentation so that incoming QC has something concrete to compare against. Mentioning the destination country at enquiry stage also lets us match the paperwork set to your import requirements.

Specification and documentation

Purity available is per batch COA (not published), with packing per order / batch confirmation (not published). Neither value is asserted in advance: every batch ships with a Certificate of Analysis carrying the measured results, so incoming QC compares against real data rather than a catalogue claim. MSDS, technical datasheets and third-party test reports can be issued for qualification purposes — state the standard you qualify against when you enquire.

Sourcing and supply

Supplier: Jinan Shenghe Chemical Co., Ltd.. For export orders, state the destination country, the transport mode and the document set you need when you enquire — packing, paperwork and quotation terms all follow from those three. Samples can be arranged for qualification, and lead time depends on stock and order size rather than on a fixed promise.

Email: info@591daili.com · Tel/WhatsApp: +86-18553102138

Frequently Asked Questions

PubChem Public Data

Source: public chemistry databases (PubChem / Wikidata) and the cited literature. Batch-dependent values are issued on the accompanying COA.