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D-SACCHARIC ACID 1,4-LACTONE

Product Name
D-SACCHARIC ACID 1,4-LACTONE
CAS No.
389-36-6
Chemical Name
D-SACCHARIC ACID 1,4-LACTONE
Synonyms
Saccharo-1,4-lactone;Sacchric acid 1,4-lactone;Saccharic acid 1,4-lactone;D-SACCHARIC ACID 1,4-LACTONE;D-SACCHARIC ACID 1 4-LACTONE 99%;D-Saccharic 1,4-lactone monohydrate;2-(3,4-dihydroxy-5-oxooxolan-2-yl)-2-hydroxyacetic acid;2-(3,4-dihydroxy-5-oxo-oxolan-2-yl)-2-hydroxy-ethanoic acid;D-(tetrahydro-2,3,4-trihydroxy-5-oxofuran-2-yl)glycollic acid;2-(3,4-dihydroxy-5-keto-tetrahydrofuran-2-yl)-2-hydroxy-acetic acid
CBNumber
CB9237812
Molecular Formula
C6H8O7
Formula Weight
192.12
MOL File
389-36-6.mol
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D-SACCHARIC ACID 1,4-LACTONE Property

Melting point:
91-93 °C(lit.)
Boiling point:
537.6±23.0 °C(Predicted)
Density 
1.961±0.06 g/cm3(Predicted)
storage temp. 
2-8°C
solubility 
H2O: 50 mg/mL, clear, colorless to faintly yellow
pka
3.28±0.11(Predicted)
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Safety

WGK Germany 
3
F 
10-21
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

American Custom Chemicals Corporation
Product number
CRB0003428
Product name
D-SACCHARIC ACID-1,4-LACTONE
Purity
95.00%
Packaging
5MG
Price
$496.89
Updated
2021/12/16
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D-SACCHARIC ACID 1,4-LACTONE Chemical Properties,Usage,Production

Definition

ChEBI: D-glucaro-1,4-lactone is a delta-lactone that is D-glucono-1,4-lactone in which the hydroxy group at position 6 has been oxidised to the corresponding carboxylic acid. It is a delta-lactone and an aldarolactone. It is functionally related to a D-glucono-1,4-lactone. It is a conjugate acid of a D-glucaro-1,4-lactone(1-).

D-SACCHARIC ACID 1,4-LACTONE Preparation Products And Raw materials

Raw materials

Preparation Products

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D-SACCHARIC ACID 1,4-LACTONE Suppliers

China 3 Germany 1 India 2 Switzerland 1 United Kingdom 1 United States 4 Global 12
Riedel-de Haen AG
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3B Scientific Corporation
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sales@3bsc.com
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United States
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MP Biomedicals, Inc.
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Pfaltz & Bauer, Inc.
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United States
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389-36-6, D-SACCHARIC ACID 1,4-LACTONERelated Search:

1,2,6-Hexanetriol Ethyl lactate D-arabinitol (S)-(+)-TETRAHYDROFURFURYL ALCOHOL γ-Valerolactone Methyl (R)-(+)-lactate (-)-1,4-ANHYDRO-L-THREITOL ISOPROPYL GLYCOLATE Diethylene glycol (+/-)-3-HYDROXY-GAMMA-BUTYROLACTONE Ethyl glycolate D-Xylose 4-Hexanolide 3-HYDROXYHEXANOIC ACID (4S,5S)-2,2-DIMETHYL-1,3-DIOXOLANE-4,5-DICARBOXYLIC ACID DIMETHYL ESTER (S)-2-HYDROXYBUTYRIC ACID D-Glyceraldehyde Dipropylene glycol

  • D-SACCHARIC ACID 1,4-LACTONE
  • D-(tetrahydro-2,3,4-trihydroxy-5-oxofuran-2-yl)glycollic acid
  • D-Saccharic 1,4-lactone monohydrate
  • D-SACCHARIC ACID 1 4-LACTONE 99%
  • Saccharic acid 1,4-lactone
  • D-Glucaric acid-1,4-lactone monohydrate, D-Saccharic acid 1,4-lactone, D-Saccharolactone
  • Saccharo-1,4-lactone
  • Sacchric acid 1,4-lactone
  • D-Glucaric acid-1,4-lactone monohydrate, D-Saccharic acid 1,4-lacton
  • 2-(3,4-dihydroxy-5-keto-tetrahydrofuran-2-yl)-2-hydroxy-acetic acid
  • 2-(3,4-dihydroxy-5-oxooxolan-2-yl)-2-hydroxyacetic acid
  • 2-(3,4-dihydroxy-5-oxo-oxolan-2-yl)-2-hydroxy-ethanoic acid
  • (S)-2-((2S,3R,4R)-3,4-Dihydroxy-5-oxotetrahydrofuran-2-yl)-2-hydroxyacetic Acid
  • (2S)-[(2S,3R,4R)-3,4-Dihydroxy-5-oxotetrahydro-2-furanyl](hydroxy)aceticacidhydrate(1:1)(non-preferredname)
  • 389-36-6
  • Carbohydrate Synthesis
  • Monosaccharides
  • Specialty Synthesis