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D-ERYTHRONOLACTONE

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CAS:15667-21-7
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Purity:98% Package:10g;100g;500g;1kg;5kg;10kg,100kg,1ton Remarks:Intermediate

D-ERYTHRONOLACTONE manufacturers

  • D-Erythronolactone
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  • $0.00 / 10G
  • 2026-05-25
  • CAS:15667-21-7
  • Min. Order: 10G
  • Purity: 98%min
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  • D-ERYTHRONOLACTONE
  • D-ERYTHRONOLACTONE pictures
  • $1.00 / 1kg
  • 2019-07-06
  • CAS:15667-21-7
  • Min. Order: 1kg
  • Purity: 98%
  • Supply Ability: 100KG
D-ERYTHRONOLACTONE Basic information
Product Name:D-ERYTHRONOLACTONE
Synonyms:(2R,3R)-BUTANE-2,3,4-TRIOL-1,4 LACTONE;(3R)-CIS-4,5-DIHYDRO-3,4-DIHYDROXY-2(3H)-FURANONE;(3R-CIS) (-)-DIHYDRO-3,4-DIHYDROXY-2(3H)-FURANONE;(3R,4R)-(-)-D-ERYTHRONOLACTONE;(3R,4R)-DIHYDROXYDIHYDRO-2(3H)-FURANONE;(3R,4R)-(-)-D-ERYTHRONOLACTONE 99.5+%;d-erythronic acid γ-lactone;D-ERYTHRONIC ACID GAMMA-LACTONE
CAS:15667-21-7
MF:C4H6O4
MW:118.09
EINECS:
Product Categories:Chiral Reagents;chiral;Biochemistry;Chiral Building Blocks;Erythrose;Simple Alcohols (Chiral);Sugar Acids;Sugars;Synthetic Organic Chemistry
Mol File:15667-21-7.mol
D-ERYTHRONOLACTONE Structure
D-ERYTHRONOLACTONE Chemical Properties
Melting point 100-102 °C(lit.)
Boiling point 140.59°C (rough estimate)
density 1.0887 (rough estimate)
refractive index -71 ° (C=1, H2O)
storage temp. Sealed in dry,Room Temperature
solubility DMSO (Slightly), Methanol (Slightly)
pka12.34±0.40(Predicted)
form Solid
color White to Off-White
Optical Rotation[α]20/D 71°, c = 1 in H2O
BRN 81073
InChI1S/C4H6O4/c5-2-1-8-4(7)3(2)6/h2-3,5-6H,1H2/t2-,3-/m1/s1
InChIKeySGMJBNSHAZVGMC-PWNYCUMCSA-N
SMILESO[C@@H]1COC(=O)[C@@H]1O
CAS DataBase Reference15667-21-7(CAS DataBase Reference)
Safety Information
Safety Statements 24/25
WGK Germany 3
HS Code 29322090
Storage Class11 - Combustible Solids
MSDS Information
ProviderLanguage
ACROS English
SigmaAldrich English
D-ERYTHRONOLACTONE Usage And Synthesis
Chemical PropertiesD-ERYTHRONOLACTONE is white to light yellow crystal powde
UsesD-erythrono-1,4-lactone is a potential substrates of dihydroxy acid dehydratase.
UsesA chiral synthon used for the synthesis of certain natural products such as the leukotrienes.
UsesD-ERYTHRONOLACTONE is a chiral synthon used for the synthesis of certain natural products such as the leukotrienes
DefinitionChEBI: Erythrono-1,4-lactone is a butan-4-olide that is dihydrofuran-2-one substituted at C-3 and C-4 by hydroxy groups (the 3R,4R-diastereomer). It is a butan-4-olide and a diol.
Synthesis
Ascorbic Acid

50-81-7

D-ERYTHRONOLACTONE

15667-21-7

Isoascorbic acid (17.6 g, 0.1 mol) was used as the raw material, which was dissolved in 250 mL of water and the solution was cooled to 0-6 °C. Anhydrous sodium carbonate powder (21.2 g, 0.2 mol) was added to the reaction flask in batches under stirring conditions. After the addition was completed, 30% hydrogen peroxide solution (22 mL) was added slowly and the internal temperature was increased from 6°C to 19°C during the reaction. Subsequently, the reaction mixture was placed in an ice bath and stirring was continued for 5 min, at which time the internal temperature increased to 27 °C. The reaction solution was heated to 42 °C and maintained at this temperature with stirring for 30 minutes. Zinc powder (1.0 g, 0.015 mol) was added to the reaction mixture and the reaction was subsequently quenched with excess hydrogen peroxide until the potassium iodide starch test paper was negative. The pH of the reaction solution was adjusted to 1.0 with 6 N hydrochloric acid. the reaction solution was concentrated to a small volume under reduced pressure at 50 °C to precipitate a white solid. Extraction was carried out with ethyl acetate (150 mL x 3), the organic phases were combined and concentrated to 200 mL (10-15 v/v). The concentrate was cooled to 15-25 °C and stirred for 5 to 8 hours to induce the precipitation of a large amount of white solid. Finally, after filtration and drying, 8.26 g (3R,4R)-3,4-dihydroxydihydrofuran-2(3H)-one was obtained in 70% yield.

Purification MethodsRecrystallise it from EtOAc (20 parts) or isoPrOH (3 parts). [Baker & MacDonald J Am Chem Soc 82 230 1960, Glattfeld & Forbrich J Am Chem Soc 56 1209 1934, Weidenhagen & Wegner Chem Ber 72 2010 1939, Musich & Rapoport J Am Chem Soc 100 4865 1978, Beilstein 18/2 V 457.]
References[1] Journal of the Chemical Society - Perkin Transactions 1, 1997, # 7, p. 1013 - 1016
[2] Patent: CN105503903, 2016, A. Location in patent: Paragraph 0270; 0271; 0272; 0273
D-ERYTHRONOLACTONE Preparation Products And Raw materials
Raw materialsErythorbic Acid-->Ascorbic Acid-->Sodium carbonate-->Hydrogen peroxide
Tag:D-ERYTHRONOLACTONE(15667-21-7) Related Product Information
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