Representative packaging image · verify the ordered lot
Decision summary
Key benefits
Defensible research value includes OXTR pharmacology, smooth-muscle and calcium-signalling models, receptor selectivity versus vasopressin receptors, neurobehavioural model design, disulfide-folding analytics and reference-standard qualification
Approved finished-drug efficacy cannot be transferred to bulk material, and “love hormone,” trust, autism, weight-loss or wellness claims are not established uses of this RUO lot.
Published research context is presented for literature orientation only. It is not a dosing, treatment or human-use instruction.
Qualification data
Specifications to confirm against the released lot
CAS
50-56-6
Formula
C43H66N12O12S2
Molecular weight
1007.2 g/mol
Appearance
Lot-specific lyophilized research peptide; confirm colour and physical form on the released-lot COA
Purity
Lot-specific chromatographic purity plus quantitative peptide content; confirm disulfide state, acetate/counterion, water and related peptides separately · target, verify batch COA
Storage
Follow the released-batch storage statement and SDS. Confirm post-opening or prepared-sample stability against the laboratory's validated protocol.
Identity, purity and content are separate release questions.
Identity
Confirm the stated molecule and supplied form. Start with the matching batch COA; request sequence-level evidence only when the buyer's written procedure requires it and availability or a separate scope has been agreed.
Purity
Review RP-HPLC method conditions, wavelength, integration and related-peak handling. A percentage without the method is not enough.
Content
Net peptide content is not the same as gross lyophilized powder weight. Ask which assay supports the stated amount and whether water/counter-ion is addressed.
Stability
Follow the storage condition stated on the batch COA or label from receipt onward.
Research context
What researchers study about Oxytocin Acetate
Oxytocin is a cyclic disulfide-bridged nonapeptide acting at the oxytocin receptor and, at some exposures, related vasopressin receptors. Named synthetic oxytocin injection finished drugs are approved for specific obstetric uses, while many intranasal social-cognition claims remain investigational and have produced mixed or negative trial results. Those approvals and studies do not make bulk oxytocin acetate an approved medicine. Lot qualification must resolve cyclic disulfide connectivity, peptide identity, acetate or other counterions and quantitative content.
Appropriate laboratory contexts include OXTR binding and signalling, receptor-selectivity studies, smooth-muscle and reproductive-tissue models, neurobehavioural models with rigorous controls, disulfide-folding and related-peptide analytics, and reference-standard work
Approved clinical indications belong to named finished drugs, not this bulk material.
Mechanism context
The question the literature is testing
Oxytocin activates OXTR-dependent G-protein and calcium signalling in appropriate models and can cross-react with vasopressin receptors depending on concentration and system. Central behavioural effects are context-dependent and not reducible to a universal bonding response. Correct intramolecular Cys1–Cys6 disulfide connectivity is central to the native cyclic structure; reduced, mispaired or intermolecular species must be analytically distinguished.
Evidence map
Research routes and exposure context
Evidence tierApproved finished-product contextResearch areaHormonal researchRoutes reported in sources
Intranasal
Dose / exposure contextProtocol-specific; verify the cited primary source
Routes and exposure contexts summarize cited studies or approved finished-product labels. They are not instructions for administering this RUO material; no customer dose is provided.
Evidence boundaries
Compatibility, limitations and decision context
Not for human or veterinary administration
Named finished-drug labels contain serious obstetric, haemodynamic and water-intoxication warnings that require clinical monitoring; they do not establish safety of bulk RUO material
Incorrect disulfide state, content or counterion, degradation, aggregation, contamination and unvalidated endotoxin or sterility are material research risks.
Interactions reported in the literature
No human combination guidance applies
SSRI, benzodiazepine, alcohol, selank, PT-141 and kisspeptin combination claims were removed from the RUO decision content
Laboratory receptor cross-reactivity or combination studies require defined systems, single-agent controls and concentration matrices.
Literature context is not a supplier release result or human-use instruction. Follow your institution's approved laboratory risk assessment.
Batch documentation
Oxytocin Acetate batch COAs
Laboratory: Manufacturer's QC laboratoryTests: HPLC purity · MS identity · endotoxin · fill amount
2 mg
5 mg
10 mg
Previews are blurred on purpose so the documents cannot be reused; third-party reports show their first page only. Sales sends the clear full version for the product and strength you ask about.
Published COAs show recent representative batches and may not be the newest. For a quote or shipment, sales confirms the lot and sends its COA.
Third-party reports, added progressively
Previews of the first page of third-party reports are on our Quality page and on the matching product pages; sales sends the full report on request. You can also send any vial from your order to an independent laboratory of your choice. Unless agreed otherwise in writing, the buyer pays for optional testing.
Help reviewing your COA
Need help reading a batch COA or third-party report? Sales can explain the test items, specifications and how the results relate to the lot under discussion.
On every batch COA: HPLC purity · MS identity · endotoxin · fill amount · Verify LyoPep
Third-party reports for Oxytocin Acetate
Reports from Qorix (tjqxgd.com), a third-party analytical laboratory in Tianjin, China: HPLC purity and MS identity of the sample tested.
Laboratory: Third-party laboratoryTests: HPLC purity · MS identity
2 mg
5 mg
Previews are blurred on purpose so the documents cannot be reused; third-party reports show their first page only. Sales sends the clear full version for the product and strength you ask about.
Ask for the current packet, not a generic certificate
Require sequence and Cys1–Cys6 disulfide-connectivity evidence, intact mass, peptide mapping where appropriate, chromatographic purity and related peptides, quantitative peptide content on a stated basis, acetate and other counterions, water, residual solvents, reduction or oxidation products, aggregation or particulates where relevant, container integrity and lot-specific stability
Appearance or a single HPLC result is insufficient.
Batch COA for the released lotHPLC purity with method contextMS identity resultEndotoxin resultFill amount (measured content per vial)SDS and handling statement
Available fills
Quote the fill and pack configuration you need
Reference SKUFillBase pack
OXYT22 mg10 vials
OT55 mg10 vials
OT1010 mg10 vials
Other format
Also available as a nasal spray (US stock)
10 mL nasal spray bottle
Besides lyophilized vials, Oxytocin Acetate is also supplied as a nasal spray solution, shipped from our US stock.
Strengths
2 mg
Bottle sizes
10 mL or 20 mL
Minimum order
10 bottles per strength and bottle size
Ships from
Our US stock
Handling
Plan storage before the parcel arrives
Follow the released-batch storage statement and SDS. Confirm post-opening or prepared-sample stability against the laboratory's validated protocol.
State the destination and timing so receipt can be planned, then move the material into its stated storage condition on arrival.
Buyer FAQ
Terms to settle before the purchase order
Can a buyer arrange third-party testing?+
Yes. You can send any vial from your order to an independent laboratory of your choice. If you want the laboratory, specification, sampling, method and acceptance rule agreed with us before testing, sales confirms them in writing. Unless otherwise agreed in writing, the buyer pays the cost of this optional testing.
What if my own lab test shows the product is out of specification?+
Send any vial from your order to an independent laboratory of your choice. If the report shows the product does not meet the specification on its COA — purity below the stated minimum, or an identity that does not match — share the report with our sales team and we refund that product in full.
Does HPLC purity prove peptide content?+
No. Chromatographic purity describes the relative peak profile under a stated method. Identity, water, counter-ion, residual solvents and assay/content may require separate methods.
How should material be stored after delivery?+
Move it into the storage condition stated on the batch COA or label as soon as it arrives, and record the package condition on receipt.
How are payment terms handled?+
Available methods and milestones depend on order value, destination and project type. The pro forma invoice should state currency, bank details, fees, payment milestones and the release condition.
Why must the testing laboratory understand peptide chemistry?+
Free-base and salt forms, hydrophilic and hydrophobic sequences, aggregation and adsorption can change sample preparation and method suitability. Use a laboratory experienced with the molecule class.
These are buyer-qualification references, not claims that this RUO material is regulated, certified or released under those frameworks. Applicability depends on the buyer's workflow and jurisdiction.
Selected sources
Literature behind the research context
Primary boundaries include the FDA Pitocin label for the named finished injection and its clinical warnings, NIH PubChem molecular identity records, and peer-reviewed receptor and clinical-trial literature. Finished-drug doses, storage and approved indications are evidence context only. Large intranasal social-cognition trials with negative primary endpoints prevent one-sided efficacy claims.
Optimal dose of oxytocin to improve social impairments and repetitive behaviors in autism spectrum disorders: meta-analysis and dose-response meta-analysis of randomized controlled trials
Frontiers in Psychiatry · 2025 · meta-analysis and dose-response meta-analysis
Why is oxytocin’s disulfide state essential to identity testing?+
Oxytocin contains an intramolecular Cys1–Cys6 disulfide bridge that defines the cyclic peptide. Qualification should combine intact mass with a method that distinguishes oxidized cyclic material from reduced, mispaired or intermolecular-disulfide species, such as peptide mapping and a qualified chromatographic comparison. A nominal mass or HPLC area value alone does not prove correct disulfide connectivity.
How should free oxytocin and oxytocin acetate be reported?+
The peptide moiety, acetate or other counterions, water and assay basis must be separated. Formula C₄₃H₆₆N₁₂O₁₂S₂ and about 1007.19 Da describe the oxytocin peptide reference, while an acetate-containing material has additional counterion mass and potentially variable stoichiometry. The COA should state whether peptide content is reported as-is, anhydrous, free-peptide equivalent or salt.
What should a laboratory request beyond a purity percentage?+
Request sequence and disulfide-connectivity evidence, intact mass, peptide mapping where appropriate, chromatographic purity and related-peptide profile, quantitative peptide content, acetate and other counterions, water, residual solvents, oxidation or reduction products, aggregation or particulates where relevant, container integrity and lot-specific stability. Endotoxin, bioburden and sterility are separate study-dependent attributes.