1-naphthaleneacetic acid is a naphthylacetic acid substituted by a carboxymethyl group at position 1.
Definition
1-naphthaleneacetic acid is a naphthylacetic acid substituted by a carboxymethyl group at position 1. It has a role as a synthetic auxin. It is a conjugate acid of a 1-naphthaleneacetate.
Source: PubChem
US FDA substance register · UNII 33T7G7757C · registered name 1-Naphthaleneacetic Acid · single chemical substance
1-Naphthaleneacetic Acid is the organic compound
Cosmetic roles
Safety & regulatory references
Not classified under Korea’s toxic-substance GHS list · existing chemical substance
More data — names, identifiers, properties, test records, literature
Names & identifiers
- CAS No.chemical registry number
- 86-87-3
- DTXSIDUS EPA chemical ID
- DTXSID8020915
- DTXCIDUS EPA compound ID
- DTXCID60915
- IUPAC
- (Naphthalen-1-yl)acetic acid
- Molecular formula
- C12H10O2
- Molecular weight
- 186.21 g/mol
Measured properties
- Appearance
- solid
- Colour
- white
- Odour
- odourless
- pH
- 4.23 (pKa)
- Melting/freezing point
- 133 ℃
- Initial boiling point and range
- 352 ℃
- Vapour pressure
- 0.0000159 ㎜Hg
- Water solubility
- 420 ㎎/ℓ
- Relative density
- 1.263
- n-Octanol/water partition coefficient (Kow)
- 2.24
- Molecular weight
- 186.21
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: KOSHA safety data sheets (Korea)
What products actually use it for
What the 3 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.
- Soil amendments1
- Softener and conditioner1
- Biocide1
Source: US EPA CompTox dashboard
Related literature
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- Consequences of NAA, BA and GA3 treatment in early fruit development phase on postharvest properties of apricot cv. NS4 · 2022
- Polyphenols profiles and antioxidant activities of extracts from Capsicum chinense in vitro plants and callus cultures · 2019
- Effects of Auxins on PIN-FORMED2 (PIN2) Dynamics Are Not Mediated by Inhibiting PIN2 Endocytosis1 · 2016
Linked databases 18
- Australian Industrial Chemicals Inventory (AICIS)
- ChEBI
- ChEMBL
- EU CosIng ingredient list 2
- Korea Cosmetic Association ingredient dictionary
- Korea toxic substances GHS register (NIER)
- KOSHA safety data sheets (Korea)
- MFDS (Korea) cosmetic ingredient register 2
- NIST Chemistry WebBook
- PubChem
- 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
- Wikipedia · English · Chinese