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InventoryRef 3466215/10/2010

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

PubChem 2D chemical structure for CAS 443-79-8
CAS 443-79-8PubChem CID 791

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

CHEBI:38264RefChem:463945DL-ISOLEUCINE2-amino-3-methyl-pentanoic acidH-DL-allo-Ile-OHIsoleucine, DL-3107-04-8DL-2-Amino-3-methylpentanoic acid
16 more reported names
Isoleucine, allo-Isoleucine, threo-L-Isoleucine, allo-L-Isoleucine, threo-L(+)-Isoleucine(2S,3S)-Alpha-amino-beta-merthylvalericacidNSC-9958Pentanoic acid, [S-(R*,R*)]-FD3037(dl)-isoleucineIsoleucine #NSC-206282(rac)-IsoleucineNorvaline, threo-AS-49219(2r,3r)-2-amino-3-methyl-pentanoic 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.

PubChem 2D chemical structure for CAS 73-32-5
CAS 73-32-5PubChem CID 6306

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

Isoleucine2S,3S-Isoleucine(S)-Isoleucine(S,S)-Isoleucine2-Amino-3-methylvaleric aciderythro-L-IsoleucineL-IleIsoleucina
16 more reported names
alpha-Amino-beta-methylvaleric acidNorvaline, 3-methyl-Valeric acid, 2-amino-3-methyl-Isoleucinumiso-leucine(2S,3S)-alpha-Amino-beta-methyl-n-valeric acid(2S,3S)-alpha-Amino-beta-merthylvaleric acid(S-(R*,R*))-2-Amino-3-methylpentanoic acid(2S,3S)-alpha-Amino-beta-merthyl-n-valeric acidNSC-46708FEMA NO. 467504Y7590D77CHEBI:17191[S-(R*,R*)]-2-Amino-3-methylpentanoic acid(2S,3S)-2-amino-3-methylpentanoateL-Isomer Isoleucine
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 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
European Commission CosIng source notes

Key data

CAS
73-32-5 / 443-79-8
EC
200-798-2 / 207-139-8
Restriction
Function
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.

Ingredients with overlapping formulation functions

Additional official and scientific sources

11 external databases to check this identity in

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

ISOLEUCINE 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, ISOLEUCINE carries the following function designation(s):

CAS 73-32-5 / 443-79-8 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 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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