Cyclamate is an organic molecular entity.
Definition
Cyclamate is an organic molecular entity.
Source: PubChem
US FDA substance register · UNII 1I6F42RME1 · registered name SODIUM CYCLAMATE · single chemical substance
Cosmetic roles
Listed as a fragrance-composition material (not a claim that it adds scent)FRAGRANCE
More data — names, identifiers, properties, test records, literature
Names & identifiers
SODIUM CYCLAMATEINCI소듐사이클라메이트Korean label name (MFDS standard)Sulfamic acid, cyclohexyl-, monosodium saltSynonym
- CAS No.chemical registry number
- 139-05-9
- EC No.EU chemical inventory number
- 205-348-9
- DTXSIDUS EPA chemical ID
- DTXSID6020355
- DTXCIDUS EPA compound ID
- DTXCID80355
- IUPAC
- Sodium cyclohexylsulfamate
- Molecular formula
- C6H12NNaO3S
- Molecular weight
- 201.22 g/mol
Measured properties
- Appearance
- Sodium cyclamate appears as odorless or almost odorless white crystals or crystalline powder. Intensely sweet taste, even in dilute solution. pH (10% solution in water): 5.5-7.5. Used as a non-nutritive sweetener. · White solid, [Hawley] White powder, [MSDSonline]
- Melting point
- 509 °F (decomposes) (NTP, 1992)
- Solubility
- greater than or equal to 100 mg/mL at 68 °F (NTP, 1992)
- Colour
- white
- Odour
- odourless
- Melting/freezing point
- 265 ℃
- Water solubility
- 210 g/㎖
- n-Octanol/water partition coefficient (Kow)
- -2.63
- Molecular weight
- 201.22
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 2 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.
- Flavouring and nutrient1
- Deodorizer1
Source: US EPA CompTox dashboard
Related literature
- In Silico Taste–Toxicity Study of New Hypothetical Hetero-Abiraterone Derivatives · 2022
- Multistage transformation of cultured rat urothelium: the effects of N-methyl-N-nitrosourea, sodium saccharin, sodium cyclamate and 12-O-tetradecanoylphorbol-13-acetate. · 1986
- Reduced trisialoganglioside synthesis in chemically but not mos-transformed mouse epidermal cells. · 1984
- Urinary bladder carcinogenesis with N-substituted aryl compounds: initiation and promotion. · 1981
Linked databases 18
- Australian Industrial Chemicals Inventory (AICIS)
- ChEBI
- ChEMBL
- China inventory of existing ingredients (IECIC)
- EU CosIng ingredient list 2
- IARC carcinogen classification
- Korea Cosmetic Association ingredient dictionary
- KOSHA safety data sheets (Korea)
- MFDS (Korea) cosmetic ingredient register 2
- PubChem 2
- Tlooto literature search 2 3 4
- 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 · Korean · English · Japanese · Chinese