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Name L-Mannono-1,4-lactone
EINECS228-678-5
CAS No. 22430-23-5
Density1.766g/cm³
PSA107.22000
LogP-3.01320
SolubilityN/A
Melting Point153-155 ºC
FormulaC6H10 O6
Boiling Point467.9°Cat760mmHg
Molecular Weight178.142
Flash Point201.5°C
Transport InformationN/A
AppearanceN/A
Safety
Risk CodesN/A
Molecular Structure
Hazard SymbolsN/A
SynonymsN/A
Article Data12

L-Mannono-1,4-lactone Synthetic route

: 74-90-8
hydrogen cyanide

: 5328-37-0
L-arabinose

A: 152772-66-2
ethyl L-mannonate

B: 22430-23-5
L-mannono-1,4-lactone

Conditions

Conditions	Yield
beim Behandeln des hesrgestellten Nitrils mit Bariumhydroxid in Wasser und Erwaermen des nach dem Ansaeuern erhaltenen Reaktionsprodukts mit Aethanol;

: 5328-37-0
L-arabinose

: 22430-23-5
L-mannono-1,4-lactone

Conditions

Conditions	Yield
With barium dihydroxide; hydrogen cyanide; water Erhitzen des Reaktionsprodukts mit Butan-1-ol unter Eindampfen;
With barium dihydroxide; hydrogen cyanide; water Erhitzen des Reaktionsprodukts mit Aethanol unter Eindampfen;
Multi-step reaction with 2 steps 2: water / durch Eindampfen View Scheme

: 133-42-6, 488-33-5, 526-95-4, 526-97-6, 576-36-3, 642-99-9, 1114-17-6, 3956-93-2, 6906-37-2, 7760-07-8, 13382-27-9, 20246-33-7, 20246-35-9, 20246-52-0, 20246-53-1, 21675-42-3, 22430-69-9, 24871-35-0, 28223-42-9, 28278-17-3, 51547-37-6
L-mannonic acid

: 22430-23-5
L-mannono-1,4-lactone

Conditions

Conditions	Yield
With water durch Eindampfen;

: 87-72-9, 608-45-7, 608-46-8, 608-47-9, 2460-44-8, 6748-95-4, 6763-34-4, 7261-26-9, 7283-06-9, 7283-07-0, 7296-55-1, 7296-56-2, 7296-58-4, 7296-59-5, 7296-60-8, 7296-61-9, 7296-62-0, 7322-30-7, 10257-31-5, 10257-32-6, 10257-33-7, 10257-34-8, 10257-35-9, 19982-83-3, 20242-88-0, 28697-53-2, 36562-42-2, 41546-41-2, 89299-64-9, 107655-34-5, 115794-06-4, 115794-07-5, 130550-15-1, 130606-21-2
L-(+)-arabinose

: 64-17-5
ethanol

: 143-33-9
sodium cyanide

A: 157663-13-3
L-gluconic acid

B: 152772-66-2
ethyl L-mannonate

C: 22430-23-5
L-mannono-1,4-lactone

Conditions

Conditions	Yield
With acetyl chloride 1) H2O, overnight, 2) r.t. to 5 deg C; Yield given. Multistep reaction;

...Expand

: 87-72-9, 608-45-7, 608-46-8, 608-47-9, 2460-44-8, 6748-95-4, 6763-34-4, 7261-26-9, 7283-06-9, 7283-07-0, 7296-55-1, 7296-56-2, 7296-58-4, 7296-59-5, 7296-60-8, 7296-61-9, 7296-62-0, 7322-30-7, 10257-31-5, 10257-32-6, 10257-33-7, 10257-34-8, 10257-35-9, 19982-83-3, 20242-88-0, 28697-53-2, 36562-42-2, 41546-41-2, 89299-64-9, 107655-34-5, 115794-06-4, 115794-07-5, 130550-15-1, 130606-21-2
L-(+)-arabinose

: 143-33-9
sodium cyanide

A: 152772-66-2
ethyl L-mannonate

B: 299-28-5, 3391-82-0, 4688-50-0, 6027-86-7, 6622-52-2, 14933-21-2, 18404-69-8, 45079-02-5, 69617-74-9, 71074-87-8, 90010-62-1, 121929-17-7
calcium L-gluconate

C: 22430-23-5
L-mannono-1,4-lactone

Conditions

Conditions	Yield
With ethanol; acetyl chloride 1) H2O, overnight, 2) r.t. to 5 deg C; Yield given. Multistep reaction;

: 112241-17-5
2,3,5,6-tetra-O-acetyl-D-galactono-1,4-lactone

: 22430-23-5
L-mannono-1,4-lactone

Conditions

Conditions	Yield
With phosphate buffer; porcine pancreatic lipase for 7h;

: 50-70-4
D-sorbitol

A: 1198-69-2
D-glucono-1,4-lactone

B: 22430-23-5
L-mannono-1,4-lactone

Conditions

Conditions	Yield
With 1-Phenylbut-1-en-3-one; rhodium hydrido (PEt3)3 complex In N,N-dimethyl-formamide at 60 - 80℃; Yield given. Yields of byproduct given;

: 67-64-1
acetone

: 22430-23-5
L-mannono-1,4-lactone

: 67642-42-6
2,3,5,6-di-O-isopropylidene-D-gulono-1,4-lactone

Conditions

Conditions	Yield
With toluene-4-sulfonic acid at 20℃; Inert atmosphere;	99%
With toluene-4-sulfonic acid In dimethoxypropane at 25℃; pH=3; Inert atmosphere;

: 22430-23-5
L-mannono-1,4-lactone

: 50-70-4
D-glucitol

Conditions

Conditions	Yield
With Cu/Cr oxide; hydrogen In ethanol at 170 - 180℃; under 90007.2 Torr; for 10h;	95%

: 67-64-1
acetone

: 22430-23-5
L-mannono-1,4-lactone

: 49561-21-9
(3aR,6S,6aR)-6-((S)-2,2-dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyldihydrofuro[3,4-d][1,3]dioxol-4(3aH)-one

Conditions

Conditions	Yield
sulfuric acid; copper(II) sulfate for 22h;	94%
With sulfuric acid; copper(II) sulfate at 20℃; for 24h;	62%

L-Mannono-1,4-lactone Chemical Properties

Molecular Structure:

Molecular Formula: C₆H₁₀O₆
Molecular Weight: 178.14
IUPAC Name: 5-(1,2-Dihydroxyethyl)-3,4-dihydroxyoxolan-2-one
Synonyms of L-Mannono-1,4-lactone (CAS NO.22430-23-5): L-Mannonic acid-gamma-lactone
CAS NO: 22430-23-5
Product Categories: 13C & 2H Sugars ; Carbohydrates & Derivatives
Melting point: 153-155 °C
Index of Refraction: 1.625
Molar Refractivity: 35.66 cm³
Molar Volume: 100.8 cm³
Surface Tension: 109.3 dyne/cm
Density: 1.766 g/cm³
Flash Point: 201.5 °C
Enthalpy of Vaporization: 84.17 kJ/mol
Boiling Point: 467.9 °C at 760 mmHg
Vapour Pressure of L-Mannono-1,4-lactone (CAS NO.22430-23-5): 1.01E-10 mmHg at 25°C

L-Mannono-1,4-lactone Safety Profile

WGK Germany of L-Mannono-1,4-lactone (CAS NO.22430-23-5): 3

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Product Name

L-Mannono-1,4-lactone

L-Mannono-1,4-lactone Synthetic route

L-Mannono-1,4-lactone Chemical Properties

L-Mannono-1,4-lactone Safety Profile

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