Gamma-aminobutyric acid is a gamma-amino acid that is butanoic acid with the amino substituent located at C-4.
How much products actually contain
No product states its amount yet.
Of the products containing it, 10 list it before the 1% line and 23 after it (usually 1% or less).
Products using this ingredient
12 of 33 confirmed · likeliest to carry enough first · See all 33
Nature RepublicNature Republic FREEMAY Olive Cica Calming Ampoule Mask Sheets
Nature RepublicNature Republic FREEMAY Olive Cica Calming Ampoule Mask Sheets (10 Sheets)
MEDIHEALDermaplus Low Molecular Hyaluronic Acid Mask 10 Sheets [Deep Moisture Charge]
Nature RepublicNature Republic FREEMAY Vegan Green Heartleaf Ampoule Mask Sheets
Nature RepublicNature Republic FREEMAY Vegan Green Heartleaf Ampoule Mask Sheets (10 Sheets)
MEDIHEALDerma 365 Mask Collagen [Firming Volume] 30 Sheets
BonajourExtreme Spot Serum
mille de fleurblanche extra concentrate serum
LAVIENLAVIEN Medinic Line Miracle Stem Exo Sphingosome Cream
MuradMurad Biome-Balancing Calm & Recover Cream
MEDIHEALDerma 365 Mask Teatree [Calming Hydra] 30 Sheets
MEDIHEALThe E.G.T Ampoule Mask 10 Sheets
Definition
Gamma-aminobutyric acid is a gamma-amino acid that is butanoic acid with the amino substituent located at C-4. It has a role as a neurotransmitter, a signalling molecule, a Saccharomyces cerevisiae metabolite and a human metabolite. It is a monocarboxylic acid and a gamma-amino acid. It is functionally related to a butyric acid. It is a conjugate acid of a gamma-aminobutyrate. It is a tautomer of a gamma-aminobutyric acid zwitterion.
Source: PubChem
US FDA substance register · UNII 2ACZ6IPC6I · registered name .GAMMA.-AMINOBUTYRIC ACID · single chemical substance
Cosmetic roles
Safety & regulatory references
Other restriction: ban substances that deplete the ozone layer
Source: EU CosIng ingredient list
More data — names, identifiers, properties, test records, literature
Official labels & definitions
JCIA labelling name アミノ酪酸: 本品は、次の化学式で表されるアミノ酸である。
Source: JCIA labelling names (Japan)
Names & identifiers
- CAS No.chemical registry number
- 56-12-2
- EC No.EU chemical inventory number
- 200-258-6
- DTXSIDUS EPA chemical ID
- DTXSID6035106
- DTXCIDUS EPA compound ID
- DTXCID4015106
- IUPAC
- 4-Aminobutanoic acid
- Molecular formula
- C4H9NO2
- Molecular weight
- 103.121 g/mol
Measured properties
- Appearance
- Solid · solid
- Melting point
- 203 °C
- Solubility
- 1300.0 mg/mL · 1.2 [ug/mL] (The mean of the results at pH 7.4)
- Dissociation constant
- 10.6
- Colour
- white
- pH
- 6.5-7.5
- Melting/freezing point
- 203 ℃
- Vapour pressure
- 0.0000000198 ㎜Hg (25 deg c)
- Water solubility
- 1300000 ㎎/ℓ (25 deg c)
- n-Octanol/water partition coefficient (Kow)
- -3.17
- Molecular weight
- 103.14
Values measured on the substance itself. The KOSHA data are a reference for writing and reviewing safety data sheets, not a specification for a commercial raw material.
Source: PubChem · KOSHA safety data sheets (Korea)
What products actually use it for
What the 6 products reported to the US EPA with this ingredient use it for. Products outside cosmetics are included, so the top few rows are its main uses.
- No specific technical function2
- Flavouring and nutrient2
- Softener and conditioner2
Source: US EPA CompTox dashboard
Irritation and sensitisation studies
2 skin studies and 2 eye studies are on record.
The study conclusions largely agree (100%). These tests are on the raw material itself; irritation at the amount in a finished product is a different question.
See all 4 studies
- Not likely to be sensitizing
skin sensitisation: in vivo (LLNA) · Screening · according to OECD Guideline 429 (Skin Sensitisation: Local Lymph Node Assay) - Category 6.3B (Category 3)
Skin Irritation · Read Across - Studies Indicate No Significant Irritation
eye irritation: in vivo · Screening · OECD Guideline 405 (Acute Eye Irritation / Corrosion) according to - Category 6.4A (Category 2A)
Eye Irritation · Read Across
Source: US EPA CompTox dashboard
Related literature
- Expression of gamma-aminobutyric acid type A receptor subunit π and minichromosome maintenance-3 in breast cancer patients treated with neoadjuvant chemotherapy: a target molecule or a proliferation marker? · 2025
- Electrochemical Determination of Eugenol Using a Poly-γ-Aminobutyric Acid Modified Glassy Carbon Electrode · 2023
- Research on Production of -Aminobutyric Acid by Lactobacillus Fermentation of Brown Rice · 2017
- gamma-Aminobutyric acid (A) receptor agonists accelerate cutaneous barrier recovery and prevent epidermal hyperplasia induced by barrier disruption. · 2002
- Glutamic Acid Decarboxylase and γ‐Aminobutyric Acid in Huntington's Disease Fibroblasts and Other Cultured Cells, Determined by a [3H]Muscimol Radioreceptor Assay · 1981
Linked databases 17
- Australian Industrial Chemicals Inventory (AICIS)
- ChEBI
- China inventory of existing ingredients (IECIC)
- EU CosIng ingredient list 2
- JCIA labelling names (Japan)
- Korea Cosmetic Association ingredient dictionary
- KOSHA safety data sheets (Korea)
- MFDS (Korea) cosmetic ingredient register 2
- NIST Chemistry WebBook
- PubChem 2
- Tlooto literature search 2 3 4 5
- UniChem cross-reference IDs
- US EPA CompTox dashboard 2
- US EPA DSSTox chemical database
- US FDA substance registration (GSRS)
- US FDA Unique Ingredient Identifier (UNII)
- Wikidata 2