For Research Purposes Only
Peptides

MT-1

★★★★ 4.7 (18 reviews)
75921-69-6alpha-MSHmelanogenesis
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$32.00

A linear synthetic analogue of alpha-MSH studied for melanogenesis pathways in preclinical research models.

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Dosage$32.00
Quantity
1

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Certificate of Analysis

Independently 3× tested by Kovera Labs — verifying identity, purity, and net content.

Pending3× Tested
PurityAwaiting results
VariantMT-1
Lot #
Labeled
Actual
Tested
Full QC PanelPending
Purity (HPLC)
Net Content
Identity (LC-MS)
Lab report in progress

MT-1 (Afamelanotide) is a full-length linear alpha-MSH analogue with selective melanocyte receptor binding. It is differentiated from shorter cyclic variants by its extended half-life and targeted interaction profile.

Studied in preclinical settings for melanogenesis pathways. 10mg/vial lyophilized powder.

Storage: 2–8°C, protected from light and moisture. 28-day shelf life post-reconstitution.

Weight 0.02 lbs
Purity

>99% HPLC Verified

Dosage

10MG

CAS

75921-69-6

Formula

C78H111N21O19

Designation

RUO

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Compound Information

Technical specifications

MOLECULAR PROFILE

What Is MT-1?

CAS Number75921-69-6
Molecular FormulaC78H111N21O19
Purity>99% HPLC Verified
FormLyophilized powder
Research GradeThird-party verified
STORAGE REQUIREMENTS

Stability Information

Avoid freeze/thaw cycles Protect from light Keep refrigerated
Lyophilized (powder)−20°C · 24+ months
Reconstituted2–8°C · ~30 days

About MT-1

  • Lyophilised powder, shipped sealed. Store refrigerated and protect from light.
  • Supplied for laboratory research use only. Not for human or veterinary use.

The GENIX Standard

  • Free shipping on every order, with no minimum.
  • Tracked delivery on every order, discreetly packaged.
  • Certificates of analysis published per lot and linked from the product page.
  • Checkout by Cash App or Zelle.
  • Research-use labelling on every vial, with no therapeutic claims made anywhere on this site.

Community Reviews

4.7 ★★★★★ Based on 18 reviews of GENIX
5 ★ 13
4 ★ 5
3 ★ 0
2 ★ 0
1 ★ 0
★★★★★

Shipping was crazy fast, got my order way sooner then expected. I also like that they have 3rd party testing available, makes the whole process feel alot more transparent. Packaging was good too.

JMJake M.
★★★★★

Really happy with the customer service. Had a question about my order and they got back to me super quick. Free shipping was also a nice bonus, didnt expect that.

STSarah T.
★★★★☆

Order came fast and everything was packaged really good. The 3rd party lab results being posted was a big reason I decided to try them. Website could be a little easier to navigate tho.

MRMike R.
★★★★★

Honestly impressed. Free shipping, quick processing and good communication thru the whole order. Customer service answered my questions without making me wait forever lol.

AKAmanda K.
★★★★★

Very smooth order from start to finish. Tracking was sent right away and package arrived quicker then I thought. I like seeing the independent testing info too, gives me more confidence in the company.

CBChris B.
★★★★★

These guys ship FAST. Ordered and had tracking basically right away. Packaging was discreet and secure, no complaints here.

TSTyler S.

Reviews are of GENIX as a supplier, not of this individual compound.

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Sources & References

Peer-reviewed research

NEW ENGLAND JOURNAL OF MEDICINE

Afamelanotide for Erythropoietic Protoporphyria

2015 · DOI: 10.1056/NEJMoa1411481 Langendonk JG, et al.
View Source ↗
AMERICAN JOURNAL OF CLINICAL DERMATOLOGY

Afamelanotide: A Review in Erythropoietic Protoporphyria

2016 Kim ES, et al.
View Source ↗
EXPERT REVIEW OF CLINICAL PHARMACOLOGY

Afamelanotide (CUV1647) in dermal phototoxicity of erythropoietic protoporphyria

2015 Minder EI, et al.
View Source ↗
BRITISH JOURNAL OF DERMATOLOGY

Systemic photoprotection in solar urticaria with alpha-melanocyte-stimulating hormone analogue [Nle4-D-Phe7]-alpha-MSH

2011 Haylett AK, et al.
View Source ↗
PHOTOCHEMISTRY AND PHOTOBIOLOGY

Mitigating photosensitivity of erythropoietic protoporphyria patients by an agonistic analog of alpha-melanocyte stimulating hormone

2009 Harms JH, et al.
View Source ↗