58846-77-8, 癸基-β-D-吡喃葡萄糖苷,
n-Decyl β-D-glucopyranoside,
CAS:58846-77-8
C16H32O6 / 320.42
MFCD00063297
Decyl b-D-glucopyranoside is a cationic surfactant, which inhibits bacterial growth by disrupting the lipid bilayer of the cell membrane. It has been used as an antimicrobial agent in the treatment of autoimmune diseases and as a preservative in cosmetics. Decyl b-D-glucopyranoside has also been shown to be effective against citric acid and sodium citrate, two common components of biofilm formation. Decyl b-D-glucopyranoside has chemical stability in both acidic and alkaline environments and is not affected by pH levels. It is also a fatty acid with a hydroxyl group and an ethylene diamine side chain.
CAS Number | 58846-77-8 |
Product Name | Decyl beta-D-glucopyranoside |
IUPAC Name | (2R,3R,4S,5S,6R)-2-decoxy-6-(hydroxymethyl)oxane-3,4,5-triol |
Molecular Formula | C16H32O6 |
Molecular Weight | 320.42 g/mol |
InChI | InChI=1S/C16H32O6/c1-2-3-4-5-6-7-8-9-10-21-16-15(20)14(19)13(18)12(11-17)22-16/h12-20H,2-11H2,1H3/t12-,13-,14+,15-,16-/m1/s1 |
InChI Key | JDRSMPFHFNXQRB-IBEHDNSVSA-N |
SMILES | CCCCCCCCCCOC1C(C(C(C(O1)CO)O)O)O |
Solubility | Soluble in DMSO |
Synonyms | Decyl glucoside; Decyl beta-D-glucoside; EINECS 261-469-7; UNII-Z17H97EA6Y; beta-D-Glucopyranoside, decyl; Decyl beta-D-glucopyranoside; n-Decyl glucoside. |
Canonical SMILES | CCCCCCCCCCOC1C(C(C(C(O1)CO)O)O)O |
Isomeric SMILES | CCCCCCCCCCO[C@H]1[C@@H]([C@H]([C@@H]([C@H](O1)CO)O)O)O |
Product name: n-Decyl β-D-glucopyranoside CAS: 58846-77-8
M.F.: C16H32O6 M.W.: 320.42
Batch No: 20120318 Quantity:50g
Items | Standards | Results |
Appearance | White powder | Complies |
MS and NMR | Should comply | Complies |
Identification | IR and TLC | Complies |
A (UV, at 260 nm) | <0.3 | Complies |
Optical activity [a ] 20D (c=1%, C2H5OH) | From -26° to -28° | -27.2° |
Loss weight on dryness | Max. 1% | 0.2% |
Residue on ignition | Max. 0.5% | 0.1% |
TLC | One spot | One spot |
Assay (HPLC) | Min. 98% | 99.1% |
References:
1. Helenius A, McCaslin DR, Fries E, Tanford C, Methods Enzymol. 1979, 56, p734-749
2. Brito RMM, Vaz WLC, Anal. Biochem. 1986, 152, 250-255
3. Brown GM, Dubreuil P, Ichhaporia FM, Desnoyers JE, Can. J. Chem. 1970, 48, 2525-2531
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