N-Cyclohexylsulfamic acid - CAS 100-88-9
Catalog: |
BB000379 |
Product Name: |
N-Cyclohexylsulfamic acid |
CAS: |
100-88-9 |
Synonyms: |
cyclohexylsulfamic acid |
Application: |
Sweetening Agents |
IUPAC Name: | cyclohexylsulfamic acid |
Description: | Cyclamic acid in the form of its sodium or calcium salt is one of the most widely used artificial sweeteners. |
Molecular Weight: | 179.24 |
Molecular Formula: | C6H13NO3S |
Canonical SMILES: | C1CCC(CC1)NS(=O)(=O)O |
InChI: | InChI=1S/C6H13NO3S/c8-11(9,10)7-6-4-2-1-3-5-6/h6-7H,1-5H2,(H,8,9,10) |
InChI Key: | HCAJEUSONLESMK-UHFFFAOYSA-N |
Melting Point: | 169.5 °C |
Purity: | > 98 % |
Density: | 1.32 g/cm3 |
Solubility: | 1 g dissolves in about 7.5 ml of water, 4 ml of alc, 4 ml of propylene glycol, Or 6 ml of acetone; slightly sol in chloroform and insol in hexane |
Appearance: | Crystals |
Decomposition: | When heated to decomposition it emits toxic fumes of sulfoxides and nitroxides |
MDL: | MFCD00065234 |
LogP: | 2.18320 |
pH: | pH of 10% aqueous solution: 0.8-1.6 |
Vapor Pressure: | 0.0000027 [mmHg] |
GHS Hazard Statement: | H315 (95.24%): Causes skin irritation [Warning Skin corrosion/irritation] |
Precautionary Statement: | P264, P280, P302+P352, P305+P351+P338, P321, P332+P313, P337+P313, and P362 |
Signal Word: | Warning |
Publication Number | Title | Priority Date |
US-10981872-B1 | Di(2-aryl hydrozonopropanal) arene derivatives | 20201027 |
US-11000534-B1 | Deuterated derivatives of psilocybin and uses thereof | 20201008 |
US-10975102-B1 | Heterocyclic diazenyl pyridinone copper(II) complexes as pharmacological antitumor agents | 20200921 |
WO-2021116503-A2 | Deuterated compounds | 20200602 |
US-10836729-B1 | Metabolically stable 5-HMF derivatives for the treatment of hypoxia | 20200504 |
PMID | Publication Date | Title | Journal |
31655124 | 20200201 | Non-nutritional sweeteners effects on endothelial vascular function | Toxicology in vitro : an international journal published in association with BIBRA |
29132732 | 20170401 | The role of artificial and natural sweeteners in reducing the consumption of table sugar: A narrative review | Clinical nutrition ESPEN |
24741154 | 20140401 | Artificial sweeteners - a review | Journal of food science and technology |
23044217 | 20121109 | Application of dispersive solid-phase extraction and ultra-fast liquid chromatography-tandem quadrupole mass spectrometry in food additive residue analysis of red wine | Journal of chromatography. A |
23000410 | 20121019 | Functional characterization of the heterodimeric sweet taste receptor T1R2 and T1R3 from a New World monkey species (squirrel monkey) and its response to sweet-tasting proteins | Biochemical and biophysical research communications |
Complexity: | 200 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 179.06161445 |
Formal Charge: | 0 |
Heavy Atom Count: | 11 |
Hydrogen Bond Acceptor Count: | 4 |
Hydrogen Bond Donor Count: | 2 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 179.06161445 |
Rotatable Bond Count: | 2 |
Topological Polar Surface Area: | 74.8 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 0.6 |
Online Inquiry
Customer Support
Customer Centered
Related Functional Groups
Sulfur Compounds
Customers Also Viewed
INDUSTRY LEADERS TRUST OUR PRODUCTS