G0754
D-Glucoheptono-1,4-lactone
≥99%
Synonym(s):
α-D-Glucoheptonic γ-lactone, D-Glycero-D-guloheptono-γ-lactone
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About This Item
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Assay
≥99%
mp
152-155 °C (lit.)
SMILES string
[H][C@]1(OC(=O)[C@H](O)[C@@H]1O)[C@H](O)[C@H](O)CO
InChI
1S/C7H12O7/c8-1-2(9)3(10)6-4(11)5(12)7(13)14-6/h2-6,8-12H,1H2/t2-,3-,4+,5-,6+/m1/s1
InChI key
VIVCRCODGMFTFY-DVKNGEFBSA-N
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Application
D-Glucoheptono-1,4-lactone may be used for the organic synthesis of N-alkyl-N-(2-hydroxyethyl)aldonamides and N-cycloalkylaldonamides.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Journal of colloid and interface science, 294(2), 423-428 (2005-09-13)
The foamability of the aqueous solutions of functionalized, surface-chemically pure surfactants of the nonionic saccharide-type: N,N-di-n-alkylaldonamides, N-alkyl-N-(2-hydroxyethyl)aldonamides, and N-cycloalkylaldonamides, derivatives of D-glucono-1,5-lactone and/or D-glucoheptono-1,4-lactone, were investigated. The approach of Lunkenheimer and Małysa for the characterization of the foamability and foam
Langmuir : the ACS journal of surfaces and colloids, 20(5), 1572-1578 (2005-04-02)
N-alkyl-N-(2-hydroxyethyl)aldonamides (alkyl: n-C6H13, n-C8H17, n-C10H21, n-C12H25, and n-C14H29) were obtained in the reaction of long-chain N-alkyl-N-(2-hydroxyethyl)amines with D-glucono-1,5-lactone and D-glucoheptono-1,4-lactone. The adsorption isotherms were obtained from surface tension measurements of aqueous solutions of surface-chemically pure surfactants. The experimental equilibrium surface
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