Val-Ala-Pro-Gly acetate salt
Val-Ala-Pro-Gly acetate salt (CAS 66835-73-2) is a peptide derivative with the empirical formula C15H26N4O5 · xC2H4O2 and a molecular weight of 342.39 (free base basis). This compound is primarily utilised as a quantitative marker in research studies focusing on human elastins. Supplied by Tech Serve Solutions, it is available for laboratory and research applications, maintaining high standards of quality for scientific investigation.

Elastin Research
Val-Ala-Pro-Gly acetate salt serves as a specific quantitative marker for the investigation of human elastins. Its use allows for precise measurement and analysis in biochemical and cell biology research.
Biochemical Assays
This peptide derivative can be employed in various biochemical assays to study protein interactions or enzymatic activity related to elastin. Its defined structure aids in reproducible experimental outcomes.
Cell Biology Studies
In cell biology, Val-Ala-Pro-Gly acetate salt is utilised to understand cellular processes involving elastin or related extracellular matrix components. It supports research into tissue development and degradation.
| Molecular weight | 342.39 (free base basis) |
|---|---|
| Empirical formula | C15H26N4O5 · xC2H4O2 |
| Assay | ≥97% (HPLC) |
| Storage temperature | −20°C |
| Application | Serves as a quantitative marker for human elastins. |
| Protective equipment | Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter |
|---|---|
| Water hazard class (WGK, DE) | 3 |
Hazard information is provided for guidance. Always consult the product Safety Data Sheet (SDS), available on request, before handling.
Documentation
Every batch ships with a Certificate of Analysis covering assay, identity and purity; the grade is confirmed against your enquiry. Safety Data Sheets and technical data sheets are available on request.
Supply & logistics
Samples for technical evaluation; bulk MOQ by grade and packaging. In-stock material ships in 7–10 working days, worldwide, with full export documentation.
What is Val-Ala-Pro-Gly acetate salt used for?
+
Val-Ala-Pro-Gly acetate salt is used as a quantitative marker for human elastins in research applications.
What is the CAS number and formula for Val-Ala-Pro-Gly acetate salt?
+
The CAS number is 66835-73-2 and the empirical formula is C15H26N4O5 · xC2H4O2.
What grade and purity does Tech Serve Solutions supply?
+
Tech Serve Solutions supplies Val-Ala-Pro-Gly acetate salt with an assay of ≥97% (HPLC). This product is supplied for research and laboratory use and is not represented as USP, BP, EP, or pharmaceutical grade.
How should Val-Ala-Pro-Gly acetate salt be handled and stored?
+
Handling requires appropriate personal protective equipment including eyeshields, gloves, and a type N95 (US) or type P1 (EN143) respirator filter. It should be stored at -20°C.
Is Val-Ala-Pro-Gly acetate salt a hazardous substance?
+
According to the German WGK classification, it has a value of 3, indicating it is hazardous to water. Appropriate safety precautions must be taken during handling and disposal.
How is this chemical packed, shipped, and exported?
+
As a specialist global supplier, Tech Serve Solutions expertly packs, handles, and exports chemicals like Val-Ala-Pro-Gly acetate salt worldwide, adhering to all relevant shipping and customs regulations.
How can I request a quote or sample?
+
To request a quote or sample of Val-Ala-Pro-Gly acetate salt, please contact our sales team via the website or directly by phone.
▶ Related products

(−)-Curcumol
C15H24O2
Cell Biology
(±) Clopidogrel hydrogensulfate
Cell Biology

(±)-L-Alliin
C6H11NO3S
Cell Biology
(±)-2-Amino-4-phosphonobutyric acid
C4H10NO5P
Cell Biology
(±)-2-Methylarachidonoyl-2′-fluoroethylamide
C23H38NOF
Cell Biology
(±)-3,4-Methylenedioxy-N-ethylamphetamine hydrochloride
Cell Biology

(±)-3,4-Methylenedioxyamphetamine hydrochloride
Cell Biology

(±)-3,4-Methylenedioxymethamphetamine hydrochloride
Cell Biology
▶ Explore more

3-Methyl-1,5-di-p-tolyl-1,4-pentazadiene
Chemical Synthesis

3-Methyl-1,5-pentanediol
Chemical Synthesis

3-Methyl-1-(2-methylphenyl)-1H-pyrazol-5-amine
C11H13N3
Chemical Synthesis
3-Methyl-1-(3′-sulfoamidophenyl)-5-pyrazolone
C10H11N3O3S
Chemical Synthesis