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InventoryRef 3766015/10/2010

SERINE

2-Amino-3-hydroxypropanoic acid

SERINE is listed in the EU CosIng inventory, but no direct annex records are linked on this page yet.

Regulatory evidence by market

No rule for this ingredient has been imported for any of the 13 markets tracked here.

That describes this inventory, not the law. No imported rule is not evidence that an ingredient is permitted: a rule may exist under another name or identifier, or in a dataset not yet imported here.

Chemical identity and properties

PubChem 2D chemical structure for CAS 302-84-1
CAS 302-84-1PubChem CID 617

DL-Serine

Serine is an alpha-amino acid that is alanine substituted at position 3 by a hydroxy group. It has a role as a fundamental metabolite. It is a polar amino acid and an alpha-amino acid. It contains a hydroxymethyl group. It is a conjugate base of a serinium. It is a conjugate acid of a serinate. It is a tautomer of a serine zwitterion. ChEBI

IUPAC name
2-amino-3-hydroxypropanoic acid
Molecular formula
C3H7NO3
Molecular weight
105.09 g/mol
Exact mass
105.042593085 Da
XLogP3
-3.1
Topological polar surface area
83.6 Ų
Hydrogen-bond donors
3
Hydrogen-bond acceptors
4
Covalent units
1
Defined stereocentres
0

Also known as

Serine, DL-00PAR1C66FNSC-9960NSC99602-azaniumyl-3-hydroxypropanoateSerine DL-RefChem:1083916206-130-6
16 more reported names
Serine DL-formH-DL-Ser-OHSERINE, (L)d,l-serineL-Serine-2-13c-15N2-amino-3-hydroxy-propanoic acidDL-2-Amino-3-hydroxypropionic AcidDL-SERINE [FCC]DL-Serine, analytical standardSERINE, L-[3-3H]DL-SERINE (1-13C)DL-Serine, Vetec(TM) reagent grade, 98%L-Serine-1,2-13C2SR-010000754742-Amion-3-hydroxypropionicacidF1652-0637
External database identifiers

Retrieved from NIH PubChem on 2026-08-31 by checksum-valid CAS matching. Chemical properties do not replace the regulatory decision on this page.

PubChem 2D chemical structure for CAS 56-45-1
CAS 56-45-1PubChem CID 5951

L-Serine

L-serine is the L-enantiomer of serine. It has a role as a mouse metabolite, a Saccharomyces cerevisiae metabolite, an Escherichia coli metabolite, a human metabolite and an algal metabolite. It is a L-alpha-amino acid, a serine, a serine family amino acid and a proteinogenic amino acid. It is a conjugate base of a L-serinium. It is a conjugate acid of a L-serinate. It is an enantiomer of a D-serine. It is a tautomer of a L-serine zwitterion. ChEBI

IUPAC name
(2S)-2-amino-3-hydroxypropanoic acid
Molecular formula
C3H7NO3
Molecular weight
105.09 g/mol
Exact mass
105.042593085 Da
XLogP3
-3.1
Topological polar surface area
83.6 Ų
Hydrogen-bond donors
3
Hydrogen-bond acceptors
4
Covalent units
1
Defined stereocentres
1

Also known as

serine(S)-2-Amino-3-hydroxypropanoic acid(S)-Serinebeta-HydroxyalanineL-(-)-SerineL-serSerinaL-Serin
16 more reported names
SER (IUPAC abbrev)Serinumalpha-Amino-beta-hydroxypropionic acidSereneL-3-Hydroxy-alaninebeta-Hydroxy-L-alanineL-2-Amino-3-hydroxypropionic acidL-3-Hydroxy-2-aminopropionic acidPropanoic acid, 2-amino-3-hydroxy-, (S)-3-Hydroxyalanine(S)-(-)-SerineCHEBI:17115(S)-alpha-Amino-beta-hydroxypropionic acid452VLY9402NSC-118365(S)-2-amino-3-hydroxy-Propanoic acid
External database identifiers

Retrieved from NIH PubChem on 2026-08-31 by checksum-valid CAS matching. Chemical properties do not replace the regulatory decision on this page.

Inventory details for SERINE

INCI name

SERINE

INN name

serine

Ph. Eur. name

serinum

Description

2-Amino-3-hydroxypropanoic acid

Record provenance

Inventory reference
37660
Imported identity
SERINE
Source update
15/10/2010
European Commission CosIng source notes

Key data

CAS
302-84-1 / 56-45-1
EC
206-130-6 / 200-274-3
Restriction
Function
ANTISTATIC
Preventing and/or reducing static electricity by neutralising electrical charge on surfaces.
FRAGRANCE
Imparting an odour or taste. Creating a perceivable pleasant smell and/or masking a bad smell.
HAIR CONDITIONING
Enhancing the appearance and feel of hair. Leaving the hair easy to comb, supple, soft and shiny and/or imparting volume, lightness, gloss, texture, etc.
SKIN CONDITIONING
Maintaining the skin in good condition.

Official EU ingredient-name evidence

The ingredient name exactly matches the official 2025 EU glossary of common ingredient names.

Ingredients with overlapping formulation functions

Additional official and scientific sources

11 external databases to check this identity in

How SERINE appears in the CosIng inventory

The CosIng inventory lists SERINE as a cosmetic ingredient and this page links it to 0 annex records. The inventory entry captures names and identifiers, while the annex records show where the substance is prohibited, restricted or positively listed in EU cosmetics law.

SERINE is also tagged with 4 cosmetic functions in the official data. Function labels describe intended use, but they do not replace regulatory review of linked annex records before formulation or labelling work.

Frequently asked questions

SERINE is listed in the EU CosIng ingredient inventory with no direct annex restriction records linked at this time. Absence of an annex link does not guarantee unrestricted use — always verify against the current official CosIng database before formulating.

According to the EU CosIng inventory, SERINE carries the following function designation(s):

CAS 302-84-1 / 56-45-1 may appear across multiple EU annex records. Viewing the CAS lookup page shows all Annex II–VI entries sharing this identifier, which is useful for identifying cross-annex regulatory status of the same chemical substance.

Use the INCI Checker to screen a full ingredient list across selected markets, or compare this substance across all supported market datasets.

Source note for SERINE

This page reproduces the CosIng inventory entry for SERINE from public European Commission cosmetic ingredient materials and shows linked identifiers even when no direct annex match is currently attached.

Use this inventory page to research SERINE and compare linked records, but verify restrictions and legal status against the current official source text and law before making regulatory decisions.

Tools & next steps

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