CAS 6322-07-2

D-Gulono-1,4-lactone

Description:

D-Gulono-1,4-lactone is a naturally occurring compound and a lactone derivative of D-gulonic acid. It is characterized by its cyclic structure, which is formed through the intramolecular esterification of the carboxylic acid and hydroxyl groups present in the D-gulonic acid molecule. This compound is a white to off-white crystalline powder that is soluble in water and exhibits a slightly sweet taste. D-Gulono-1,4-lactone plays a significant role in the biosynthesis of ascorbic acid (vitamin C) in certain organisms, acting as an intermediate in the metabolic pathway. It is also utilized in the food industry as a flavoring agent and a potential antioxidant. The compound has a relatively low toxicity profile, making it safe for consumption in appropriate amounts. Its stability can be influenced by factors such as pH and temperature, which are important considerations in both industrial applications and biological contexts. Overall, D-Gulono-1,4-lactone is an important compound with various applications in nutrition and food science.

Formula: C₆H₁₀O₆

InChI: InChI=1/C6H10O6/c7-1-2(8)5-3(9)4(10)6(11)12-5/h2-5,7-10H,1H2/t2-,3+,4-,5+/m1/s1

InChI key: InChIKey=SXZYCXMUPBBULW-LECHCGJUSA-N

SMILES: [C@H](CO)(O)[C@]1([C@@H](O)[C@@H](O)C(=O)O1)[H]

Synonyms:

• (3R,4S,5S)-5-[(1R)-1,2-Dihydroxyethyl]-3,4-dihydroxyoxolan-2-one
• (3R,4S,5S)-5-[(1R)-1,2-dihydroxyethyl]-3,4-dihydroxydihydrofuran-2(3H)-one (non-preferred name)
• 1,4-<span class="text-smallcaps">D</span>-Gulonolactone
• <span class="text-smallcaps">D</span>-Gulonic acid, γ-lactone
• <span class="text-smallcaps">D</span>-Gulonic γ-lactone
• <span class="text-smallcaps">D</span>-Gulono-1,4-lactone
• <span class="text-smallcaps">D</span>-Gulono-γ-lactone
• <span class="text-smallcaps">D</span>-Gulonolactone
• D-(-)-Gulonic acid G-lactone
• D-(-)-Gulono-1,4-lactone
• D-Gulonic Acid-1,4-Lactone
• D-gulonic gamma-lactone
• Gulonic acid, γ-lactone, <span class="text-smallcaps">D</span>-
• NSC 34392
• γ-<span class="text-smallcaps">D</span>-Gulonolactone
• 1,4-D-Gulonolactone
• γ-D-Gulonolactone
• Gulonic acid, γ-lactone, D-
• D-(-)-Gulono-1,4-lactone, D-Gulono γ-lactone, D-Gulono-1,4-lactone
• (3R)-3α,4α-Dihydroxy-5α-[(1R)-1,2-dihydroxyethyl]-4,5-dihydrofuran-2(3H)-one
• gulonic gamma-lactone
• D-gulo-Hexonic acid 1,4-lactone
• D-GULONOLACTONE
• D(-)-GULONIC ACID GAMMA-LACTONE
• D-(-)-GULONO-GAMMA-LACTONE
• 5-(1,2-DIHYDROXY-ETHYL)-3,4-DIHYDROXY-DIHYDRO-FURAN-2-ONE
• D-GULONO-1,4-LACTONE extrapure
• D-GULONO-GAMMA-LACTONE
• D-GULONIC ACID GAMMA-LACTONE

D-Gulonic acid-1,4-lactone, 98%

CAS: 6322-07-2

D-Gulono-1,4-lactone is a hexanoic acid used as a starting material in EPC syntheses. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item

Formula: C₆H₁₀O₆

Purity: 98%

Molecular weight: 178.14

Ref: 02-J66987

D-(-)-Gulonic acid γ-lactone

CAS: 6322-07-2

Formula: C₆H₁₀O₆

Purity: 98%

Color and Shape: Solid

Molecular weight: 178.1400

Ref: IN-DA003A7O

D-Gulonic acid-1,4-lactone

CAS: 6322-07-2

Molecular weight: 178.14

Ref: 7W-GC2044

D(-)-Gulonic Acid γ-Lactone

CAS: 6322-07-2

D(-)-Gulonic Acid γ-Lactone

Purity: 97%

Molecular weight: 178.14g/mol

Ref: 54-OR1012752

1,4-D-Gulonolactone

CAS: 6322-07-2

1,4-D-Gulonolactone

Purity: ≥98%

Molecular weight: 178.14g/mol

Ref: 54-BUP19042

1,4-D-Gulonolactone

CAS: 6322-07-2

1,4-D-Gulonolactone, precursor to vitamin C, is an enzyme substrate linked to oxidative stress and absent in scurvy-susceptible species.

Formula: C₆H₁₀O₆

Purity: 99.69%

Color and Shape: White Or Off-White Crystalline Powder

Molecular weight: 178.14

Ref: TM-T4719

D-Gulonic acid-1,4-lactone

CAS: 6322-07-2

D-Gulonic acid-1,4-lactone is a naturally occurring compound that is formed from L-gulonic acid and a 1,4-lactone ring. It has been shown to have inhibitory properties against the matrix metalloproteinases MMP-2 and MMP-9. It also has an effect on dehydroascorbic acid, which plays an important role in the regulation of bioavailability of vitamin C. D-Gulonic acid-1,4-lactone has been found to stimulate collagen synthesis in human skin cells, which may be due to its ability to increase the activity of enzymes such as pyruvate kinase and lactate dehydrogenase. The structural analysis of this compound reveals a pyrazole ring with two hydroxyl groups (OH).

Formula: C₆H₁₀O₆

Purity: Min. 98 Area-%

Color and Shape: White Powder

Molecular weight: 178.14 g/mol

Ref: 3D-MG05225

(3R,4S,5S)-5-((R)-1,2-Dihydroxyethyl)-3,4-dihydroxydihydrofuran-2(3H)-one

CAS: 6322-07-2

Formula: C₆H₁₀O₆

Purity: 95%

Color and Shape: Solid

Molecular weight: 178.14

Ref: 10-F054363

D-Gulono-1,4-Lactone extrapure, 98%

CAS: 6322-07-2

Formula: C₆H₁₀O₆

Purity: min.98%

Color and Shape: White to off-white, Crystalline powder

Molecular weight: 178.14

Ref: SR-11777

D-Gulono-1,4-lactone

Controlled Product

CAS: 6322-07-2

Applications D-Gulono-1,4-lactone (cas# 6322-07-2) is a compound useful in organic synthesis.

Formula: C₆H₁₀O₆

Color and Shape: Neat

Molecular weight: 178.14

Ref: TR-G854995