ISOLEUCINE
L-Isoleucine; DL-allo-Isoleucine; 2-Amino-3-methylpentanoic acid
ISOLEUCINE 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

2-Amino-3-methylpentanoic acid
2-amino-3-methylpentanoic acid is a branched chain amino acid that consists of 3-methylpentanoic acid bearing an amino substituent at position 2. It is a branched-chain amino acid and an alpha-amino acid. — ChEBI
- IUPAC name
- 2-amino-3-methylpentanoic acid
- Molecular formula
- C6H13NO2
- Molecular weight
- 131.17 g/mol
- Exact mass
- 131.094628657 Da
- XLogP3
- -1.7
- Topological polar surface area
- 63.3 Ų
- Hydrogen-bond donors
- 2
- Hydrogen-bond acceptors
- 3
- Covalent units
- 1
- Defined stereocentres
- 0
Also known as
16 more reported names
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.

L-Isoleucine
L-isoleucine is the L-enantiomer of isoleucine. It has a role as a mouse metabolite, a Saccharomyces cerevisiae metabolite, a plant metabolite, an Escherichia coli metabolite, a human metabolite and an algal metabolite. It is a L-alpha-amino acid, an aspartate family amino acid, an isoleucine and a proteinogenic amino acid. It is a conjugate base of a L-isoleucinium. It is a conjugate acid of a L-isoleucinate. It is an enantiomer of a D-isoleucine. It is a tautomer of a L-isoleucine zwitterion. — ChEBI
- IUPAC name
- (2S,3S)-2-amino-3-methylpentanoic acid
- Molecular formula
- C6H13NO2
- Molecular weight
- 131.17 g/mol
- Exact mass
- 131.094628657 Da
- XLogP3
- -1.7
- Topological polar surface area
- 63.3 Ų
- Hydrogen-bond donors
- 2
- Hydrogen-bond acceptors
- 3
- Covalent units
- 1
- Defined stereocentres
- 2
Also known as
16 more reported names
External database identifiers
- ChEBI:CHEBI:17191
- ChEMBL:CHEMBL1233584
- EPA DTXSID:DTXSID1047441
- EPA DTXSID:DTXSID2046882
- PubMed:40885242
- PubMed:39172838
- PubMed:31926187
- PubMed:29968805
- PubMed:23108620
- PubMed:23107499
- PubMed:23105881
- PubMed:23088461
- PubMed:23084640
- PubMed:23079773
- PubMed:23061283
- PubMed:23056478
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 ISOLEUCINE
INCI name
ISOLEUCINE
INN name
isoleucine
Description
L-Isoleucine; DL-allo-Isoleucine; 2-Amino-3-methylpentanoic acid
Record provenance
- Inventory reference
- 34662
- Imported identity
- ISOLEUCINE
- Source update
- 15/10/2010
Annex records for ISOLEUCINE
Key data
- ANTISTATIC
- Preventing and/or reducing static electricity by neutralising electrical charge on surfaces.
- 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.
Related inventory evidence
Ingredients with overlapping formulation functions
Additional official and scientific sources
11 external databases to check this identity in
Each link searches that source for this identity. What each source is, and its legal weight
How ISOLEUCINE appears in the CosIng inventory
The CosIng inventory lists ISOLEUCINE 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.
ISOLEUCINE is also tagged with 3 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
Source note for ISOLEUCINE
This page reproduces the CosIng inventory entry for ISOLEUCINE 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 ISOLEUCINE 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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