6014-42-2

Basic information

• Product Name: 6-DEOXY-L-MANNOSE MONOHYDRATE
• Synonyms: L-(+)-RHAMNOSE HYDRATE;L-RHA H2O;L-(+)-RHAMMNOSE MONOHYDRATE;L-(+)-RHAMNOPYRANOSE, MONOHYDRATE;L-(+)-RHAMNOSE;ISODULCIT;ISODULCIT MONOHYDRATE;6-DEOXY-L-MANNOSE HYDRATE
• CAS NO: 6014-42-2
• Molecular Formula: C₆H₁₂O₅
• Molecular Weight: 182.17
• Mol File: 6014-42-2.mol
• Article Data: 104

Chemical Properties

• Melting Point: 91-93 °C
• Boiling Point: 323.9±42.0 °C(Predicted)
• Appearance: /
• Density: 1.556±0.06 g/cm3(Predicted)
• PKA: 12.28±0.70(Predicted)
• CAS DataBase Reference: 6-DEOXY-L-MANNOSE MONOHYDRATE(CAS DataBase Reference)
• NIST Chemistry Reference: 6-DEOXY-L-MANNOSE MONOHYDRATE(6014-42-2)
• EPA Substance Registry System: 6-DEOXY-L-MANNOSE MONOHYDRATE(6014-42-2)

Safety Data

• Safety Statements: 24/25
• Hazardous Substances Data: 6014-42-2(Hazardous Substances Data)

Usage

Definition

ChEBI: An L-rhamnopyranose having alpha-configuration at the anomeric centre.

Upstream product

• 20188-85-6 7,4′-di-O-methylquercetin-3-O-beta-rutinoside 
• 20562-03-2 α-chaconine 
• 20562-02-1 solanine 
• 849758-42-5 3-O-β-D-glucopyranosyl-(1->6)-β-D-glucopyranosyl-(1->6)-β-D-glucopyranosyl-2β,3β,16α,23,24-pentahydroxyolean-12-ene-28-oic acid 28-O-β-D-xylopyranosyl-(1->4)-α-L-rhamnopyranosyl-(1->2)-α-L-arabinopyranoside 
• 1246030-28-3 3α,11α,30-trihydroxylup-20(29)-en-23,28-dioic acid 28-O-[α-L-rhamnopyranosyl-(1->4)-β-D-glucopyranosyl-(1->6)-β-D-glucopyranosyl]ester 
• 1246030-30-7 3α,19β,O-dihydroxylupane-23,28-dioic acid 28-O-[α-L-rhamnopyranosyl-(1->4)-β-D-glucopyranosyl-(1->6)-β-D-glucopyranosyl]ester 
• 10236-47-2 naringin 
• 1260388-60-0 (2β,3β,4α)-3-(β-D-glucopyranosyloxy)-2,27-dihydroxyolean-12-ene-23,28-dioic acid 28-[O-β-D-galactopyranosyl-(1->3)-β-D-xylopyranosyl-(1->4)-6-deoxy-α-L-mannopyranosyl-(1->2)-6-deoxy-β-D-galactopyranosyl] ester 
• 1260388-58-6 (2β,3β,4α)-3-(β-D-glucopyranosyloxy)-2,27-dihydroxyolean-12-ene-23,28-dioic acid 28-{O-β-D-xylopyranosyl-(1->4)-O-6-deoxy-α-L-mannopyranosyl-(1->2)-O-[β-D-glucopyranosyl-(1->3)]-6-deoxy-4-O-[3-(3,4-dimethoxyphenyl)-1-oxoprop-2-en-1-yl]-β-D-galactopyranosyl} ester 
• 1260388-59-7 (2β,3β,4α)-3-(β-D-glucopyranosyloxy)-2,27-dihydroxyolean-12-ene-23,28-dioic acid 28-{O-β-D-galactopyranosyl-(1->4)-O-β-D-xylopyranosyl-(1->4)-O-3-O-acetyl-6-deoxy-α-L-mannopyranosyl-(1->2)-O-[β-D-glucopyranosyl-(1->3)]-6-deoxy-4-O-[3-(3,4-dimethoxyphenyl)-1-oxoprop-2-en-1-yl]-β-D-galactopyranosyl} ester 
• 1393523-96-0 6,7-methylenedioxy-3,5,4'-trihydroxyflavone 3-O-α-L-rhamnopyranosyl-(1->2)[β-D-glucopyranosyl-(1->6)]-β-D-glucopyranoside 
• 1420652-41-0 [(benzoxy)methyl]phenyl-4-O-α-L-rhamnopyranosyl-(1→6)-?-D-glucopyranoside 

Downstream Products

• 42927-37-7 6-deoxy-talose-(methyl-phenyl-hydrazone) 
• 100300-50-3 rhamnose-phenylbenzylhydrazone 
• 14479-23-3 N-phenyl-rhamnopyranosylamine 
• 99886-59-6 Rhamnose-dibenzyldithioacetal 
• 645-50-1 rhamnose-phenylhydrazone 
• 7707-85-9 pyruvaldehyde bis-phenylhydrazone 
• 108691-56-1 6-deoxy-L-gulose-(4-bromo-phenylhydrazone) 
• 6748-70-5 L-rhamnose diethyl dithioacetal 
• 14917-55-6 methyl 6-deoxy-α-L-mannopyranoside 
• 65310-00-1 (3S,4R,5S,6S)-2-methoxy-6-methyltetrahydro-2H-pyran-3,4,5-triol 
• 57472-03-4 methyl β-L-fucofuranoside 
• 57472-02-3 methyl α-L-fucofuranoside 
• 14687-15-1 methyl L-fucopyranoside 
• 1128-40-1 methyl β-L-fucopyranoside 

Relevant articles and documents

New triterpenoids from the red sea sponge Siphonochalina siphonella

Clear differences were found when comparing the chemical content of the northern, Gulf of Eilat, to the southern-central, Dahlak archipelago, Red Sea sponge Siphonochalina siphonella. The Dahlak sponge was found to be richer in the more polar triterpenes. Nine new compounds (1-4, 7, 8, 15-17) were isolated and identified, among them two sipholane glycosides, sipholenoside A and B (7 and 8), and one compound, dahabinone A (17), possessing a new skeleton.

Exopolysaccharide Produced by Probiotic Bacillus albus DM-15 Isolated From Ayurvedic Fermented Dasamoolarishta: Characterization, Antioxidant, and Anticancer Activities

An exopolysaccharide (EPS) was purified from the probiotic bacterium Bacillus albus DM-15, isolated from the Indian Ayurvedic traditional medicine Dasamoolarishta. Gas chromatography-mass spectrophotometry and nuclear magnetic resonance (NMR) analyses revealed the heteropolymeric nature of the purified EPS with monosaccharide units of glucose, galactose, xylose, and rhamnose. Size-exclusion chromatography had shown the molecular weight of the purified EPS as around 240 kDa. X-ray powder diffraction analysis confirmed the non-crystalline amorphous nature of the EPS. Furthermore, the purified EPS showed the maximum flocculation activity (72.80%) with kaolin clay and emulsification activity (67.04%) with xylene. In addition, the EPS exhibits significant antioxidant activities on DPPH (58.17 ± 0.054%), ABTS (70.47 ± 0.854%) and nitric oxide (58.92 ± 0.744%) radicals in a concentration-dependent way. Moreover, the EPS showed promising cytotoxic activity (20 ± 0.97 μg mL–1) against the lung carcinoma cells (A549), and subsequent cellular staining revealed apoptotic necrotic characters in damaged A549 cells. The EPS purified from the probiotic strain B. albus DM-15 can be further studied and exploited as a potential carbohydrate polymer in food, cosmetic, pharmaceutical, and biomedical applications.

Flavonoids and Naphthoquinones from Juglans nigra Bark

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