L-(+)-Gulose - ≥98% , CAS No.6027-89-0

CAS: 6027-89-0 Cat. No.: G120861 Formula: C6H12O6 Peso molecolare: 180.16 Numero EC: 27-897-3
Disponibile su ordine
GRADE & PURITY ≥98%
Synonyms
L-Gulose | SCHEMBL284703 | (2S,3S,4R,5S)-2,3,4,5,6-pentahydroxyhexanal | GZCGUPFRVQAUEE-JGWLITMVSA-N | MFCD00136022 | C16055 | Gulose, L- | Q27117231 | L-GULOSE [MI] | A869013 | s6180 | HY-128394 | AKOS027320511 | EINECS 227-897-3 | DTXSID401342718 | J96E
Storage
Protected from light,Store at -20°C
Shipped In
Ice chest + Ice pads
★
Size
Germania (EU)
USA*
Price
Qty
10mg
G120861-10mg
—
3 Disponibile
123,13€
25mg
G120861-25mg
—
3 Disponibile
235,94€
50mg
G120861-50mg
—
2 Disponibile

345,27€

425,11€
Salva 79,83 € (18.78%)
100mg
G120861-100mg
—
3 Disponibile

551,80€

764,39€
Salva 212,60 € (27.81%)
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Protected from light,Store at -20°C Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Panoramica

L-(+)-Gulose, a rare aldohexose sugar C-3 epimer of galactose, is used in the development of various drugs and to glycosylate alginates. L-(+)-Gulose is a substrate of GDP-mannose 3′,5′-epimerase in plants and may be a precursor of L-ascorbic acid in plants.

Specifications

Sinonimi
L-Gulose | SCHEMBL284703 | (2S,3S,4R,5S)-2,3,4,5,6-pentahydroxyhexanal | GZCGUPFRVQAUEE-JGWLITMVSA-N | MFCD00136022 | C16055 | Gulose, L- | Q27117231 | L-GULOSE [MI] | A869013 | s6180 | HY-128394 | AKOS027320511 | EINECS 227-897-3 | DTXSID401342718 | J96E
Specifiche e purezza
≥98%
Condizioni di conservazione di stoccaggio
Protected from light,Store at -20°C
Spedito in
Ice chest + Ice pads
Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.
Purezza
≥98%
Nomi e identificatori
Pubchem Sid504755440
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504755440
Sorrisi canoniciC(C(C(C(C(C=O)O)O)O)O)O
IUPAC Name(2S,3S,4R,5S)-2,3,4,5,6-pentahydroxyhexanal
InChIKeyGZCGUPFRVQAUEE-JGWLITMVSA-N
INCHI1S/C6H12O6/c7-1-3(9)5(11)6(12)4(10)2-8/h1,3-6,8-12H,2H2/t3-,4+,5-,6-/m1/s1
Isomeri SMILES C([C@@H]([C@H]([C@@H]([C@@H](C=O)O)O)O)O)O
WGK Germania 3
Peso molecolare 180.16
Reaxy-Rn 1908976
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1908976&ln=

Documentazione

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic oxygen compounds
ClasseOrganooxygen compounds
SubclassCarbohydrates and carbohydrate conjugates
Intermediate Tree Nodes Monosaccharides
Direct ParentHexoses
Alternative Parents Medium-chain aldehydes  Beta-hydroxy aldehydes  Alpha-hydroxyaldehydes  Secondary alcohols  Polyols  Primary alcohols  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAliphatic acyclic compounds
Substituents Hexose monosaccharide - Medium-chain aldehyde - Beta-hydroxy aldehyde - Alpha-hydroxyaldehyde - Secondary alcohol - Polyol - Organic oxide - Hydrocarbon derivative - Primary alcohol - Carbonyl group - Aldehyde - Alcohol - Aliphatic acyclic compound
DescrizioneThis compound belongs to the class of organic compounds known as hexoses. These are monosaccharides in which the sugar unit is a is a six-carbon containing moeity.
External Descriptors aldehydo-gulose - L-gulose
Struttura 3D
Modello di struttura chimica interattiva





Certificati (CoA, COO, BSE/TSE e tabella di analisi)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

5 results found

Lot NumberCertificate TypeDataOggetto
F2520126Certificate of AnalysisJun 25, 2025 G120861
I2214571Certificate of AnalysisJun 30, 2022 G120861
I2214702Certificate of AnalysisJun 30, 2022 G120861
I2214748Certificate of AnalysisJun 30, 2022 G120861
I2214749Certificate of AnalysisJun 30, 2022 G120861
Proprietà chimiche e fisiche
Sensibilitàlight sensitive
Rotazione specifica [α]25° (C=0.5,H2O)
Punto di fusione (°C)132 °C
Peso molecolare180.160 g/mol
XLogP3-2.900
Hydrogen Bond Donor Count5
Hydrogen Bond Acceptor Count6
Rotatable Bond Count5
Exact Mass180.063 Da
Monoisotopic Mass180.063 Da
Topological Polar Surface Area118.000 Ų
Heavy Atom Count12
Formal Charge0
Complexity138.000
Isotope Atom Count0
Defined Atom Stereocenter Count4
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Calcolatori di soluzioni
Recensioni

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