L-Arabinose supplier | CasNO.5328-37-0

Name
L-Arabinose
EINECS 226-214-6
CAS No. 5328-37-0
Article Data302
CAS DataBase
Density 1.508g/cm3
Solubility almost transparency
Melting Point 155ºC
Formula C₅H₁₀O₅
Boiling Point 415.5ºC at 760mmHg
Molecular Weight 150.131
Flash Point 219.2ºC
Transport Information
Appearance white crystalline powder
Safety
Risk Codes
Molecular Structure
Hazard Symbols
Synonyms Arabinose,L- (8CI);(+)-Arabinose;L-(+)-Arabinose;NSC 1941;
PSA 97.99000
LogP -2.73970

Synthetic route

: ducheside B

A: 51768-38-8
3-O-methylellagic acid

B: 5328-37-0
L-arabinose

Conditions

Conditions	Yield
With hydrogenchloride In 1,4-dioxane at 80℃; for 1h;	A 85% B n/a

: 3,3′,4′-tri-O-methylellagic acid 4-O-α-L-arabinofuranoside

A: 5328-37-0
L-arabinose

B: 1617-49-8
3,3',4-tri-O-methylellagic acid

Conditions

Conditions	Yield
With hydrogenchloride In 1,4-dioxane at 80℃; for 1h;	A n/a B 88%

: 3-O-methylellagic acid 4-O-α-L-arabinofuranoside

A: 51768-38-8
3-O-methylellagic acid

B: 5328-37-0
L-arabinose

Conditions

Conditions	Yield
With hydrogenchloride In 1,4-dioxane at 80℃; for 1h;	A 78% B n/a

: C27H28O16

A: 5328-37-0
L-arabinose

B: 3615-41-6
L-Rhamnose

C: 3,4′-O-dimethyl ellagic acid

Conditions

Conditions	Yield
With hydrogenchloride In 1,4-dioxane at 80℃; for 1h;	A n/a B n/a C 88%

...Expand

: ellagic acid 3-O-α-L-rhamnopyranosyl-4′-O-α-L-arabinofuranoside

A: 5328-37-0
L-arabinose

B: 3615-41-6
L-Rhamnose

C: 476-66-4
ellagic acid

Conditions

Conditions	Yield
With hydrogenchloride In 1,4-dioxane at 80℃; for 1h;	A n/a B n/a C 77%

...Expand

Ganoderma capense heteropolysaccharide GCPB-2, 1.03E5 Da: Ganoderma capense heteropolysaccharide GCPB-2, 1.03E5 Da

A: 58-86-6
D-xylose

B: 5328-37-0
L-arabinose

Conditions

Conditions	Yield
With trifluoroacetic acid In water at 120℃; for 6h; Sealed tube;

: 4-O-(α-L-arabinopyranosyl) nervogenic acid lindelofidine ester

: 5328-37-0
L-arabinose

Conditions

Conditions	Yield
With hydrogenchloride In 1,4-dioxane; water at 90℃; for 4h;

: 4-O-(α-L-arabinopyranosyl) nervogenic acid laburnine ester

: 5328-37-0
L-arabinose

Conditions

Conditions	Yield
With hydrogenchloride In 1,4-dioxane; water at 90℃; for 4h;

: 3-[(3-hydroxy-3-methylbutyl)-4-O-(α-L-arabinopyranosyl)]-5-(3-methyl-2-butenyl) benzoate lindelofidine ester

: 5328-37-0
L-arabinose

Conditions

Conditions	Yield
With hydrogenchloride In 1,4-dioxane; water at 90℃; for 4h;

: (12R,20S,23S,24R)-20,25-dihydroxy-23,24-epoxy-12-O-α-L-arabinopyranosyl-3,4-secodammara-4(28)-en-3-oic acid

: 5328-37-0
L-arabinose

Conditions

Conditions	Yield
With hydrogenchloride In water at 100℃; for 3h;

: (23E)-(20S)-(3α,12β)-20-hydroxy-dammara-23,25-dien-12-O-α-L-arabinopyranoside-3-O-α-L-arabinopyranoside

: 5328-37-0
L-arabinose

Conditions

Conditions	Yield
With hydrogenchloride In water at 100℃; for 3h;

: 3α-[(α-L-arabinopyranosyl)-oxy]-24(S),25-dihydroxy-30-oxo-lanost-8-ene

: 5328-37-0
L-arabinose

Conditions

Conditions	Yield
With hydrogenchloride In water at 80℃; for 6h;

: 4-O-[β-D-glucopyranosyl-(1→2)-α-L-arabinopyranosyl] nervogenic acid lindelofidine ester

A: 5328-37-0
L-arabinose

B: 50-99-7
D-glucose

Conditions

Conditions	Yield
With hydrogenchloride In 1,4-dioxane; water at 90℃; for 4h;

: phyllaemblicins H4

A: 5328-37-0
L-arabinose

B: 50-99-7
D-glucose

Conditions

Conditions	Yield
With hydrogenchloride In water at 80℃; for 6h; Sealed tube;

: 3-O-α-L-arabinopyranosyl-phytolaccagenin-28-O-β-D-glucopyranosyl ester

A: 5328-37-0
L-arabinose

B: 50-99-7
D-glucose

Conditions

Conditions	Yield
With potassium hydroxide In water for 2h; Reflux;
With hydrogenchloride In water at 90℃; for 3h;

: trilliumoside A

A: 5328-37-0
L-arabinose

B: 3615-41-6
L-Rhamnose

Conditions

Conditions	Yield
With trifluoroacetic acid In 1,4-dioxane; water at 90℃; for 3h;

: trilliumoside B

A: 5328-37-0
L-arabinose

B: 3615-41-6
L-Rhamnose

Conditions

Conditions	Yield
With trifluoroacetic acid In 1,4-dioxane; water at 90℃; for 3h;

: trilliumoside C

A: 5328-37-0
L-arabinose

B: 3615-41-6
L-Rhamnose

Conditions

Conditions	Yield
With trifluoroacetic acid In 1,4-dioxane; water at 90℃; for 3h;

: trilliumoside D

A: 5328-37-0
L-arabinose

B: 3615-41-6
L-Rhamnose

Conditions

Conditions	Yield
With trifluoroacetic acid In 1,4-dioxane; water at 90℃; for 3h;

: trilliumoside E

A: 5328-37-0
L-arabinose

B: 3615-41-6
L-Rhamnose

Conditions

Conditions	Yield
With trifluoroacetic acid In 1,4-dioxane; water at 90℃; for 3h;

: trilliumoside F

A: 5328-37-0
L-arabinose

B: 3615-41-6
L-Rhamnose

Conditions

Conditions	Yield
With trifluoroacetic acid In 1,4-dioxane; water at 90℃; for 3h;

: trilliumoside G

A: 5328-37-0
L-arabinose

B: 3615-41-6
L-Rhamnose

Conditions

Conditions	Yield
With trifluoroacetic acid In 1,4-dioxane; water at 90℃; for 3h;

: trilliumoside H

A: 5328-37-0
L-arabinose

B: 3615-41-6
L-Rhamnose

Conditions

Conditions	Yield
With trifluoroacetic acid In 1,4-dioxane; water at 90℃; for 3h;

: (20S)-(3α,12β)-20-hydroxy-dammara-24-dien-12-O-β-D-quinovopyranoside-3-O-α-L-arabinopyranoside

A: 5328-37-0
L-arabinose

B: 7658-08-4
D-quionovose

Conditions

Conditions	Yield
With hydrogenchloride In water at 100℃; for 3h;

: 3α-[(α-L-rhamnopyranosyl)-oxy]-24(S)-[(α-L-arabinopyranosyl)-oxy]-25-hydroxylanost-8-en-30-oic acid

A: 5328-37-0
L-arabinose

B: 3615-41-6
L-Rhamnose

Conditions

Conditions	Yield
With hydrogenchloride In water at 80℃; for 6h;

: (3S,12R,17R,20S,21S)-3-O-[β-D-glucopyranosyl-(1→2)-α-L-arabinopyranosyl]-12-hydroxy-19-oxo-18,19-secours-13(18)-en-28,21-lactone

A: 5328-37-0
L-arabinose

B: 50-99-7
D-glucose

Conditions

Conditions	Yield
Stage #1: (3S,12R,17R,20S,21S)-3-O-[β-D-glucopyranosyl-(1→2)-α-L-arabinopyranosyl]-12-hydroxy-19-oxo-18,19-secours-13(18)-en-28,21-lactone With trifluoroacetic acid at 120℃; for 1.5h; Stage #2: With (S)-1-amino-2-propanol; sodium cyanoborohydride; acetic acid In methanol at 65℃; for 1.5h; Stage #3: With pyridine; acetic anhydride at 100℃; for 0.75h;

: (3S,12R,17R,19S,20S,21S)-3-O-[β-D-glucopyranosyl-(1→2)-α-L-arabinopyranosyl]-12,19-dihydroxy-18,19-secours-13(18)-en-28,21-lactone

A: 5328-37-0
L-arabinose

B: 50-99-7
D-glucose

Conditions

Conditions	Yield
Stage #1: (3S,12R,17R,19S,20S,21S)-3-O-[β-D-glucopyranosyl-(1→2)-α-L-arabinopyranosyl]-12,19-dihydroxy-18,19-secours-13(18)-en-28,21-lactone With trifluoroacetic acid at 120℃; for 1.5h; Stage #2: With (S)-1-amino-2-propanol; sodium cyanoborohydride; acetic acid In methanol at 65℃; for 1.5h; Stage #3: With pyridine; acetic anhydride at 100℃; for 0.75h;

: 3β-O-[β-D-glucopyranosyl-(1→2)-α-L-arabinopyranosyl]-19α-hydroxy-olean-12-en-28-oic acid

A: 5328-37-0
L-arabinose

B: 50-99-7
D-glucose

Conditions

Conditions	Yield
Stage #1: 3β-O-[β-D-glucopyranosyl-(1→2)-α-L-arabinopyranosyl]-19α-hydroxy-olean-12-en-28-oic acid With trifluoroacetic acid at 120℃; for 1.5h; Stage #2: With (S)-1-amino-2-propanol; sodium cyanoborohydride; acetic acid In methanol at 65℃; for 1.5h; Stage #3: With pyridine; acetic anhydride at 100℃; for 0.75h;

: coreoside B

A: 5328-37-0
L-arabinose

B: 50-99-7
D-glucose

C: C14H18O3

Conditions

Conditions	Yield
With hydrogenchloride; water In methanol at 85℃; for 15h;

...Expand

: 3-O-α-L-rhamnopyranosyl-(1→3)-β-D-xylopyranosyl-(1→3)-α-L-rhamnopyranosyl-(1→2)-α-L-arabinopyranosyl hederagenin

A: 58-86-6
D-xylose

B: 5328-37-0
L-arabinose

C: 3615-41-6
L-Rhamnose

Conditions

Conditions	Yield
With hydrogenchloride In water at 90℃; for 6h;

...Expand

: 5328-37-0
L-arabinose

: 108-24-7
acetic anhydride

: 5139-19-5
2,3,4,5-tetra-O-acetyl-L-arabinose

Conditions

Conditions	Yield
In pyridine at 50℃; for 10h; Acetylation;	100%
With pyridine; N-Bromosuccinimide; hydrogen cation; ethanethiol Multistep reaction;

: 5328-37-0
L-arabinose

: L-arabinonitrile

Conditions

Conditions	Yield
With phenoxyamine hydrochloride In aq. phosphate buffer; water-d2 at 20℃; for 12h;	100%

: 5328-37-0
L-arabinose

: 57-14-7
1,1-dimethylhydrazine

: (2S,3R,4S,E)-5-(2,2-dimethylhydrazono)pentane-1,2,3,4-tetraol

Conditions

Conditions	Yield
With Amberlyst 15 In methanol at 20℃; for 24h;	99%

: 5328-37-0
L-arabinose

: 75-08-1
ethanethiol

: 43179-48-2
L-arabinose di(ethylthio)acetal

Conditions

Conditions	Yield
With dimethylbromosulphonium bromide at 0 - 5℃; for 0.416667h; neat (no solvent);	96%
Stage #1: ethanethiol With hydrogenchloride In water at 0℃; Stage #2: L-arabinose In water for 1h;	92%
In hydrogenchloride at 0℃; for 0.5h;	91%

: 5328-37-0
L-arabinose

: 2547-08-2
L-xylulose 1-phosphate

Conditions

Conditions	Yield
With Thermotoga maritima MSB8 L-rhamnulose kinase; Bacillus subtilis L-arabinose isomerase; Pseudomonas Sp, ST-24 D-tagatose 3-epimerase; ATP; sodium hydroxide pH=7.5; Enzymatic reaction;	96%
With Pseudomonas Sp. St-24 D-tagatose 3-epimerase; Thermotoga maritima MSB8 L-arabinose isomerase; Thermotoga maritima MSB8 L-rhamnulose kinase; magnesium(II); manganese(II); ATP at 45℃; pH=Ca. 7.5; Enzymatic reaction;

: 5328-37-0
L-arabinose

: 479-27-6
naphthalene-1,8-diamine

: 73858-38-5
(1S,2R,3S)-1-(2,3-Dihydro-1H-perimidin-2-yl)-butane-1,2,3,4-tetraol

Conditions

Conditions	Yield
In ethanol; water; acetic acid for 2h; Heating;	95%

: 5328-37-0
L-arabinose

: 109-76-2
Trimethylenediamine

: hexahydro-2-(L-arabino-1,2,3,4-tetrahydroxybutyl)pyrimidine

Conditions

Conditions	Yield
for 69h; Cyclization;	95%

: 5328-37-0
L-arabinose

: 67-64-1
acetone

: 27820-98-0
1,2;3,4-di-O-isopropylidene-β-L-arabinopyranose

Conditions

Conditions	Yield
With sulfonated polystyrene cation exchange resin CAT600 at 40℃; for 3h; Green chemistry;	95%
With malonic acid; choline chloride for 0.333333h; Reflux; Green chemistry;	92%

: 5328-37-0
L-arabinose

: 108-98-5
thiophenol

: 28697-82-7
(2S,3S,4R)-5,5-bis(phenylthio)pentane-1,2,3,4-tetraol

Conditions

Conditions	Yield
With trifluoroacetic acid In water at 50 - 60℃; for 12h;	95%

: 5328-37-0
L-arabinose

: 123506-40-1
6-hydrazino-1,3-dimethyl-1H-pyrimidine-2,4-dione

: 69471-91-6
1,3-Dimethyl-6-{N'-[(2S,3R,4S)-2,3,4,5-tetrahydroxy-pent-(Z)-ylidene]-hydrazino}-1H-pyrimidine-2,4-dione

Conditions

Conditions	Yield
In methanol for 5h; Heating;	93%

: 116989-58-3
6-(hydrazinocarbonylmethyl)-6H-indolo[2,3-b]quinoxaline

: 5328-37-0
L-arabinose

: L-arabinose (6-indolo[2,3-b]quinoxalin-6-yl)acetylhydrazone

Conditions

Conditions	Yield
With acetic acid In ethanol; water for 0.2h; microwave irradiation;	93%

: 5328-37-0
L-arabinose

: 5358-18-9
(2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-acetic acid hydrazide

: C11H16N4O7

Conditions

Conditions	Yield
With acetic acid In ethanol; water for 5h; Heating;	93%

: 5328-37-0
L-arabinose

: 16596-41-1
N-aminopyrrolidine

: (2S,3R,4S)-5-(pyrrolidin-1-ylimino)pentane-1,2,3,4-tetrol

Conditions

Conditions	Yield
In methanol for 3h; Reflux;	93%

: 5328-37-0
L-arabinose

: L-ribulose 1-phosphate

Conditions

Conditions	Yield
With Bacillus subtilis L-arabinose isomerase; human fructosekinase; ATP; sodium hydroxide pH=7.5; Enzymatic reaction;	93%
With Human fructokinase; Thermotoga maritima MSB8 L-arabinose isomerase; magnesium(II); manganese(II); ATP at 37℃; pH=Ca. 7.5; Enzymatic reaction;

: 1000071-56-6
2-(5-methyl-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)acetohydrazide

: 5328-37-0
L-arabinose

: C12H18N4O7

Conditions

Conditions	Yield
With acetic acid In ethanol; water for 5h; Heating;	92%

: 5328-37-0
L-arabinose

: D-ribulose 5-phosphate

Conditions

Conditions	Yield
With Bacillus subtilis L-arabinose isomerase; L-ribulose kinase; ATP; sodium hydroxide pH=7.5; Enzymatic reaction;	92%

: 107-03-9
1-thiopropane

: 5328-37-0
L-arabinose

: 121471-02-1
L-arabinose dipropyl dithioacetal

Conditions

Conditions	Yield
With dimethylbromosulphonium bromide at 0 - 5℃; for 0.666667h; neat (no solvent);	91%
With hydrogenchloride

: 5328-37-0
L-arabinose

: 67399-25-1
N-Methyl-N-(4-phenyl-thiazol-2-yl)hydrazin

: 120191-88-0
L-Arabinose-N-methyl-N-(4-phenyl-thiazol-2-yl)hydrazon

Conditions

Conditions	Yield
In ethanol; acetic acid for 24h; Ambient temperature;	91%

: 5328-37-0
L-arabinose

: 67399-25-1
N-Methyl-N-(4-phenyl-thiazol-2-yl)hydrazin

: (2S,3R,4S)-5-[Methyl-(4-phenyl-thiazol-2-yl)-hydrazono]-pentane-1,2,3,4-tetraol

Conditions

Conditions	Yield
In ethanol; acetic acid for 24h; Ambient temperature;	91%

: 5328-37-0
L-arabinose

: 112357-63-8
N-Methyl-N-<4-(p-chlor-phenyl)-thiazol-2-yl>hydrazin

: (2S,3R,4S)-5-{[4-(4-Chloro-phenyl)-thiazol-2-yl]-methyl-hydrazono}-pentane-1,2,3,4-tetraol

Conditions

Conditions	Yield
In ethanol; acetic acid for 24h; Ambient temperature;	91%

: 5328-37-0
L-arabinose

: 98-88-4
benzoyl chloride

A: 7473-44-1
1,2,3,4-tetra-O-benzoyl-β-L-arabinopyranose

B: 202415-33-6
1,2,3,5-tetra-O-benzoyl-α-L-arabinofuranose

Conditions

Conditions	Yield
With pyridine; dmap at 25℃;	A 91% B 1%

...Expand

: 5328-37-0
L-arabinose

: 98-88-4
benzoyl chloride

: 7473-44-1
1,2,3,4-tetra-O-benzoyl-β-L-arabinopyranose

Conditions

Conditions	Yield
With pyridine; dmap at 20℃;	90%
With pyridine

: 5328-37-0
L-arabinose

: 112357-62-7
N-Methyl-N-<4-(p-brom-phenyl)-thiazol-2-yl>hydrazin

: (2S,3R,4S)-5-{[4-(4-Bromo-phenyl)-thiazol-2-yl]-methyl-hydrazono}-pentane-1,2,3,4-tetraol

Conditions

Conditions	Yield
In ethanol; acetic acid for 24h; Ambient temperature;	90%

: 5328-37-0
L-arabinose

: 100-53-8
phenylmethanethiol

: 40733-11-7
L-arabinose dibenzyl dithioacetal

Conditions

Conditions	Yield
With hydrogenchloride	88%
With hydrogenchloride for 0.5h;	87%
With hydrogenchloride

: 5328-37-0
L-arabinose

: 98-88-4
benzoyl chloride

: 212499-83-7
1',2',3',4'-tetra-O-benzoyl-α/β-L-arabinopyranose

Conditions

Conditions	Yield
In pyridine; dichloromethane at 20℃;	88%

: 1041404-16-3
(N4-acetylcytosin-1-yl)acetohydrazine

: 5328-37-0
L-arabinose

: L-(+)-arabinose 2-[4-acetamido-2-oxopyrimidin-1(2H)-yl]acetylhydrazone

Conditions

Conditions	Yield
With acetic acid In ethanol; water Heating;	88%

: 5328-37-0
L-arabinose

: 21383-24-4
(5,6-diphenyl-[1,2,4]triazin-3-yl)-hydrazine

: (2S,3R,4S)-5-[(5,6-Diphenyl-[1,2,4]triazin-3-yl)-hydrazono]-pentane-1,2,3,4-tetraol

Conditions

Conditions	Yield
In methanol; water for 0.333333h; Heating;	87%

: 5328-37-0
L-arabinose

: 86799-26-0
2-hydrazineyl-6-phenylpyrimidin-4(3H)-one

: 6-Phenyl-2-{N'-[(2S,3R,4S)-2,3,4,5-tetrahydroxy-pent-(E)-ylidene]-hydrazino}-3H-pyrimidin-4-one

Conditions

Conditions	Yield
In ethanol; water for 0.25h; Condensation; Heating;	87%

L-Arabinose Chemical Properties

IUPAC Name: (2S,3R,4S,5S)-Oxane-2,3,4,5-tetrol
Following is the structure of L-Arabinose (CAS NO.5328-37-0):

Empirical Formula: C₅H₁₀O₅
Molecular Weight: 150.1299
Index of Refraction: 1.646
Molar Refractivity: 31.02 cm³
Molar Volume: 85.4 cm³
Density: 1.757 g/cm³
Flash Point: 155.3 °C
Melting point: 160-163 °C(lit.)
Surface Tension: 75.3 dyne/cm
Enthalpy of Vaporization: 66.74 kJ/mol
Boiling Point: 333.2 °C at 760 mmHg
Solubility: H₂O: 1 M at 20 °C, clear, colorless
Stability: Stable. Incompatible with strong oxidizing agents.
Vapour Pressure of L-Arabinose (CAS NO.5328-37-0): 9.92E-06 mmHg at 25 °C
Product Categories of L-Arabinose (CAS NO.5328-37-0): CARBOHYDRATE; Arabinose; Basic Sugars (Mono & Oligosaccharides); Biochemistry; Sugars; Biochemicals and Reagents; BioUltraBiochemicals and Reagents; Carbohydrate LibraryResearch Essentials; CarbohydrateMetabolomics; CarbohydratesCarbohydrates; Metabolic Pathways; Metabolites and Cofactors on the Metabolic Pathways Chart; Carbohydrates; Carbohydrates A to; Carbohydrates A-CBiochemicals and Reagents; Core Bioreagents; Metabolic Libraries; Monosaccharide; Specialty Synthesis; Carbohydrate Synthesis; Monosaccharides; MonosaccharideSpecialty Synthesis
Appearance: white crystalline powder
Canonical SMILES: C1C(C(C(C(O1)O)O)O)O
Isomeric SMILES: C1[C@@H]([C@@H]([C@H]([C@H](O1)O)O)O)O
InChI: InChI=1S/C5H10O5/c6-2-1-10-5(9)4(8)3(2)7/h2-9H,1H2/t2-,3-,4+,5-/m0/s1
InChIKey: SRBFZHDQGSBBOR-KLVWXMOXSA-N

L-Arabinose Uses

L-Arabinose (CAS NO.5328-37-0) is a very important operon in molecular biology and bioengineering.

L-Arabinose Safety Profile

WGK Germany: 3
F: 3-10

L-Arabinose Specification

L-Arabinose , its cas register number is 5328-37-0. It also can be called L(+)Arabinose; Amidosulfonic acid; 4-Dimethylaminobenzalrhodanine ; and L-Arabinopyranose .

Product Name

L-Arabinose

Synthetic route

L-Arabinose Chemical Properties

L-Arabinose Uses

L-Arabinose Safety Profile

L-Arabinose Specification

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