N-Acetyl-DL-serine
N-Acetyl-DL-serine (CAS: 97-14-3; C5H9NO4) is a modified amino acid with a molecular weight of 147.13 g/mol. This compound serves as a valuable building block in biochemical research and organic synthesis. Its structural characteristics lend it to various applications within the scientific community, particularly in the development of novel compounds and in academic research settings where precise molecular structures are required for experimentation.

Biochemical Research
N-Acetyl-DL-serine is utilised in academic and industrial research laboratories for studies involving amino acid derivatives and their biological interactions. It serves as a reagent for exploring biochemical pathways and enzyme mechanisms.
Organic Synthesis
As a modified amino acid, it can be employed as a chiral building block or intermediate in complex organic synthesis projects. Its structure is useful for creating more intricate molecules with defined stereochemistry.
Peptide Chemistry
This compound may find application in peptide synthesis, either as a modified residue or as a tool for investigating the properties of peptides containing serine analogues. Research into modified peptides can explore altered biological activity or stability.
| Molecular weight | 147.13 |
|---|---|
| Empirical formula | C5H9NO4 |
| Storage temperature | −20°C |
| 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 N-Acetyl-DL-serine used for?
+
N-Acetyl-DL-serine is primarily used in biochemical research and organic synthesis as a modified amino acid building block.
What is the CAS number and formula for N-Acetyl-DL-serine?
+
The CAS number is 97-14-3 and the empirical formula is C5H9NO4.
What grade and purity does Tech Serve Solutions supply?
+
Tech Serve Solutions supplies N-Acetyl-DL-serine as a research-grade chemical. The specific assay and purity are not detailed in the provided data, and it is not represented as USP, BP, or EP grade.
How should N-Acetyl-DL-serine be handled and stored?
+
Handling requires appropriate personal protective equipment, including eyeshields, gloves, and a type N95 (US) or P1 (EN143) respirator filter. It should be stored at -20°C.
Is N-Acetyl-DL-serine a controlled substance?
+
The provided data does not indicate that N-Acetyl-DL-serine is a controlled substance.
How can I get a quote or sample?
+
Please contact our sales team directly through our website or by phone to request a quote or a sample of N-Acetyl-DL-serine.
How is N-Acetyl-DL-serine shipped?
+
N-Acetyl-DL-serine is suitable for export and is shipped according to standard chemical handling procedures, requiring storage at -20°C.
▶ Related products
![(±)-(E)-4-Ethyl-2-[(E)-hydroxyimino]-5-nitro-3-hexenamide (C8H13N3O4) — chemical structure, CAS 138472-01-2; Biochemicals & Reagents, fine chemical supplied by Tech Serve Solutions](/_next/image?url=https%3A%2F%2Fpub-f4d920c906024441a773a96f7098e551.r2.dev%2Fimages%2Fproducts%2F138472-01-2.png&w=3840&q=75)
(±)-(E)-4-Ethyl-2-[(E)-hydroxyimino]-5-nitro-3-hexenamide
C8H13N3O4
Biochemicals & Reagents![(±)-(E)-4-Ethyl-2-[(Z)-hydroxyimino]-5-nitro-3-hexen-1-yl-nicotinamide (C14H18N4O4) — chemical structure, CAS 162626-99-5; Biochemicals & Reagents, fine chemical supplied by Tech Serve Solutions](/_next/image?url=https%3A%2F%2Fpub-f4d920c906024441a773a96f7098e551.r2.dev%2Fimages%2Fproducts%2F162626-99-5.png&w=3840&q=75)
(±)-(E)-4-Ethyl-2-[(Z)-hydroxyimino]-5-nitro-3-hexen-1-yl-nicotinamide
C14H18N4O4
Biochemicals & Reagents
(±)-2,5-Dimethoxy-4-bromoamphetamine hydrobromide
Biochemicals & Reagents

(±)-2-(p-Methoxyphenoxy)propionic acid
C10H12O4
Biochemicals & Reagents
(±)-2-Amino-6,7-dihydroxy-1,2,3,4-tetrahydronaphthalene hydrobromide
C10H13NO2·HBr
Biochemicals & Reagents
(±)-2-Hydroxydecanoic acid
C10H20O3
Biochemicals & Reagents
(±)-3-Hydroxydecanoic acid
C10H20O3
Biochemicals & Reagents
(±)-3-Hydroxyoctanoic acid
C8H16O3
Biochemicals & Reagents▶ 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