D(+)-Xylose supplier | CasNO.58-86-6

Name
D(+)-Xylose
EINECS 200-400-7
CAS No. 58-86-6
Article Data433
CAS DataBase
Density 1.525
Solubility soluble
Melting Point 154-158°C(lit.)
Formula C₅H₁₀O₅
Boiling Point 331oC
Molecular Weight 150.131
Flash Point 219.2oC
Transport Information
Appearance White crystal powder
Safety 24/25-36-26
Risk Codes 36/37/38
Molecular Structure
Hazard Symbols Xi
Synonyms Xylose, D-(8CI);(+)-Xylose;D-(+)-Xylose;Wood sugar;
PSA 90.15000
LogP -2.58230

Synthetic route

xylan: xylan

: 58-86-6
D-xylose

Conditions

Conditions	Yield
With hydrogenchloride; water at 105℃; for 3h; Ionic liquid;	77%
With water at 60℃; for 3h;	73 %Chromat.

xylan: xylan

A: 58-86-6
D-xylose

B: 1114-34-7
D-lyxose

Conditions

Conditions	Yield
With hydrogenchloride; sodium molybdate dihydrate In water for 0.05h; Sealed tube; Microwave irradiation;	A 60% B 31%

xylan: xylan

A: 98-01-1
furfural

B: 58-86-6
D-xylose

Conditions

Conditions	Yield
With water In toluene at 170℃; for 6h; Inert atmosphere;	A 18% B 27%
With (2E)-but-2-enedioic acid In water at 160℃; for 4h; Reagent/catalyst; Temperature; Inert atmosphere; Autoclave; Industrial scale;	A 24.4% B 25.4%

: 22416-58-6
β-D-Xylp-(1-4)-β-D-Xylp-(1-4)-β-D-Xylp-(1-4)-β-D-Xyl

: 58-86-6
D-xylose

Conditions

Conditions	Yield
With maize β-xylosidase for 6h; aq. acetate buffer; Enzymatic reaction;
With recombinant β-xylosidase/α-L-arabinofuranosidase/β-glucosidase from Cellulosimicrobium cellulans sp. 21 In aq. phosphate buffer at 30℃; for 0.166667h; pH=8; Enzymatic reaction;
Multi-step reaction with 2 steps 1: polyethylenimine-coated Selenomonas ruminantium β-xylosidase immobilized on glyoxyl agarose; water / aq. acetate buffer / 0.08 h / 50 °C / pH 5 / Enzymatic reaction 2: polyethylenimine-coated Selenomonas ruminantium β-xylosidase immobilized on glyoxyl agarose; water / aq. acetate buffer / 2 h / 50 °C / pH 5 / Enzymatic reaction View Scheme

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;

: β-D-xylopyranoside

A: 58-86-6
D-xylose

B: 472-11-7
(25R)-ruscogenin

Conditions

Conditions	Yield
With hydrogenchloride In 1,4-dioxane; water at 95℃; for 1h; Inert atmosphere;	A n/a B 3.8 mg

: phyllaemblicins H3

A: 58-86-6
D-xylose

B: 50-99-7
D-glucose

Conditions

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

: phyllaemblicin H10

A: 58-86-6
D-xylose

B: 50-99-7
D-glucose

Conditions

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

: 47592-59-6
β-D-Xylp-(1-4)-β-D-Xylp-(1-4)-D-Xyl

: 58-86-6
D-xylose

Conditions

Conditions	Yield
With recombinant β-xylosidase/α-L-arabinofuranosidase/β-glucosidase from Cellulosimicrobium cellulans sp. 21 In aq. phosphate buffer at 30℃; for 0.166667h; pH=8; Enzymatic reaction;
Multi-step reaction with 2 steps 1: polyethylenimine-coated Selenomonas ruminantium β-xylosidase immobilized on glyoxyl agarose; water / aq. acetate buffer / 2 h / 50 °C / pH 5 / Enzymatic reaction 2: polyethylenimine-coated Selenomonas ruminantium β-xylosidase immobilized on glyoxyl agarose; water / aq. acetate buffer / 2 h / 50 °C / pH 5 / Enzymatic reaction View Scheme

: (20S,24R)-(3α,12β)-20,24-epoxy-dammara-25-hydroxyl-12-O-β-D-quinovopyranoside-3-O-β-D-xylopyranoside

A: 58-86-6
D-xylose

B: 7658-08-4
D-quionovose

Conditions

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

: (22R,23S,25R,26R)-spirost-5-ene-3β,23,26-triol 3-O-β-D-xylopyranosyl-(1 → 3)-β-D-glucopyranoside

A: 58-86-6
D-xylose

B: 50-99-7
D-glucose

Conditions

Conditions	Yield
With hydrogenchloride In water at 90℃; for 2h;

: (24R,25S)-3β-[(O-β-D-glucopyranosyl-(1→2)-O-[β-D-xylopyranosyl-(1→3)]-β-D-galactopyranosyl)oxy]-24-hydroxy-5β-spirostan-12-one.

A: 58-86-6
D-xylose

B: 50-99-7
D-glucose

C: 59-23-4
D-Galactose

Conditions

Conditions	Yield
With hydrogenchloride; water In 1,4-dioxane at 95℃; for 2h; Inert atmosphere;

...Expand

: (25R)-3β-hydroxyspitost-5-en-1β-yl O-α-L-rhamnopyranosyl-(1→2)-O-[β-D-xylopyranosyl-(1→3)]-β-D-xylopyranoside

A: 58-86-6
D-xylose

B: 3615-41-6
L-Rhamnose

C: 472-11-7
(25R)-ruscogenin

Conditions

Conditions	Yield
With hydrogenchloride In 1,4-dioxane; water at 95℃; for 1h; Inert atmosphere;	A n/a B n/a C 2.8 mg

...Expand

beechwood xylan: beechwood xylan

: 58-86-6
D-xylose

Conditions

Conditions	Yield
With Thermomyces lanuginosus xylanase; recombinant β-xylosidase/α-L-arabinofuranosidase/β-glucosidase from Cellulosimicrobium cellulans sp. 21 In aq. phosphate buffer at 37℃; for 8h; pH=8; Reagent/catalyst; Enzymatic reaction;

: 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

: 3β-O-D-xylopyranosyl-30-norolean-12,20(29)-dien-28-oic acid 28-O-β-D-glucopyranosyl ester

A: 58-86-6
D-xylose

B: 50-99-7
D-glucose

Conditions

Conditions	Yield
With hydrogenchloride In water at 95℃; for 2h;

: C42H64O15

A: 58-86-6
D-xylose

B: 50-99-7
D-glucose

Conditions

Conditions	Yield
With hydrogenchloride In water at 95℃; for 2h;

: (20S*,24R*)-20,24-epoxy-15α,23β,25-trihydroxy-3β-(β-D-xylopyranosyloxy)-9,19-cycloart-7-en-16-one

: 58-86-6
D-xylose

Conditions

Conditions	Yield
With hydrogenchloride In water at 80 - 90℃; for 1h;

: 11-dehydro-15α-hydroxyximicidol-3-O-β-D-xylopyranoside

: 58-86-6
D-xylose

Conditions

Conditions	Yield
With hydrogenchloride In water at 80 - 90℃; for 1h;

: (23R,24R)-16β,23;16α,24-diepoxycycloart-7-en-3β,12β,15α,25-tetraol 3-O-β-D-xylopyranoside

: 58-86-6
D-xylose

Conditions

Conditions	Yield
With hydrogenchloride In water at 80 - 90℃; for 1h;

: thaliside C

A: 58-86-6
D-xylose

B: 50-99-7
D-glucose

Conditions

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

: 87-99-0
XYLITOL

: 58-86-6
D-xylose

Conditions

Conditions	Yield
With Yarrowia lipolytica short chain dehydrogenase/reductase; nicotinamide adenine dinucleotide phosphate; magnesium chloride In aq. buffer at 28℃; for 0.166667h; pH=8.0; Enzymatic reaction;

: 3β-[(O-β-D-glucopyranosyl-(1→2)-O-[β-D-xylopyranosyl-(1→3)]-β-D-galactopyranosyl)oxy]-5β-spirost-25(27)-en-12-one

A: 58-86-6
D-xylose

B: 50-99-7
D-glucose

C: 59-23-4
D-Galactose

D: 3β-hydroxy-5β-spirost-25(27)-en-12-one

Conditions

Conditions	Yield
With hydrogenchloride; water In 1,4-dioxane at 95℃; for 2h; Inert atmosphere;	A n/a B n/a C n/a D 2.9 mg

...Expand

: (25R)-3β-[(O-β-D-glucopyranosyl-(1→2)-O-[β-D-xylopyranosyl-(1→3)]-β-D-galactopyranosyl)oxy]-5β-spirostan-12-one

A: 58-86-6
D-xylose

B: 50-99-7
D-glucose

C: 59-23-4
D-Galactose

D: 38676-82-3
(25R)-3β-hydroxy-5β-spirostan-12-one

Conditions

Conditions	Yield
With hydrogenchloride; water In 1,4-dioxane at 95℃; for 2h; Inert atmosphere;	A n/a B n/a C n/a D 3 mg

...Expand

: 49694-21-5
xylohexaose

: 58-86-6
D-xylose

Conditions

Conditions	Yield
With recombinant β-xylosidase/α-L-arabinofuranosidase/β-glucosidase from Cellulosimicrobium cellulans sp. 21 In aq. phosphate buffer at 30℃; for 0.166667h; pH=8; Enzymatic reaction;

: 3β-O-α-L-rhamnopyranosyl-(1→2)-[β-D-xylopyranosyl-(1→4)]-β-D-glucopyranosyl-homo-aro-cholest-5-ene-26-O-β-D-glucopyranoside

A: 58-86-6
D-xylose

B: 3615-41-6
L-Rhamnose

C: 50-99-7
D-glucose

D: homo-aro-cholest-5-ene-3β,26-diol

Conditions

Conditions	Yield
With hydrogenchloride In 1,4-dioxane; water at 95℃; for 2h; Inert atmosphere;	A n/a B n/a C n/a D 5 mg

...Expand

: 3-O-α-L-rhamnopyranosyl-(1→3)-β-D-xylopyranosyl-(1→3)-α-L-rhamnopyranosyl-(1→2)-α-L-arabinopyranosyl hederagenin 28-O-β-D-glucopyranosyl ester

A: 58-86-6
D-xylose

B: 5328-37-0
L-arabinose

C: 3615-41-6
L-Rhamnose

D: 50-99-7
D-glucose

Conditions

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

...Expand

: 58-86-6
D-xylose

: 87-99-0
XYLITOL

Conditions

Conditions	Yield
With hydrogen In water at 120℃; under 15001.5 Torr; for 0.166667h; Temperature; Pressure;	100%
With sodium tetrahydroborate In water at 20℃; for 3h;	88%
With hydrotalcite; Pt/γ-Al2O3; hydrogen In water at 60℃; under 12001.2 Torr; for 4h; Catalytic behavior; Reagent/catalyst; Time; Green chemistry;	79%

: 67-56-1
methanol

: 58-86-6
D-xylose

: 1824-96-0, 1824-97-1, 3795-68-4, 3795-69-5, 4229-54-3, 5531-18-0, 7473-45-2, 13039-63-9, 13039-64-0, 13039-65-1, 13039-67-3, 22416-73-5, 22861-09-2, 25129-51-5, 52485-92-4, 52689-55-1, 52689-56-2, 56607-40-0, 72880-70-7, 79083-42-4, 86782-30-1, 86782-31-2, 89615-03-2, 89673-67-6, 89707-99-3, 102045-32-9, 135910-17-7
methyl xylofuranoside

Conditions

Conditions	Yield
Stage #1: methanol; D-xylose With hydrogenchloride In water for 12h; Stage #2: With calcium carbonate In water at 20℃;	100%
With trifluoroacetic acid Ambient temperature;
With hydrogenchloride In water at 30℃; for 3.5h;
Stage #1: methanol; D-xylose With hydrogenchloride at 55℃; for 21h; Stage #2: With silver carbonate In methanol at 25℃; for 0.5h;

: 58-86-6
D-xylose

: 111-86-4
n-Octylamine

: 67669-28-7
C13H27NO4

Conditions

Conditions	Yield
In methanol at 45℃;	100%

: 58-86-6
D-xylose

: 2627-86-3
(S)-1-phenyl-ethylamine

: 1361940-04-6
C13H19NO4

Conditions

Conditions	Yield
In methanol at 45℃;	100%

: 58-86-6
D-xylose

: 3886-69-9
(R)-1-phenyl-ethyl-amine

: 1361940-02-4
C13H19NO4

Conditions

Conditions	Yield
In methanol at 45℃;	100%

: 58-86-6
D-xylose

: 108-91-8
cyclohexylamine

: 95585-48-1
C11H21NO4

Conditions

Conditions	Yield
In methanol at 45℃;	100%

: 58-86-6
D-xylose

: 109-73-9
N-butylamine

: 82002-00-4
N-D-Xylosyl-n-butylamin

Conditions

Conditions	Yield
In methanol at 45℃;	100%

: 58-86-6
D-xylose

: 107-11-9
1-amino-2-propene

: 1361940-06-8
C8H15NO4

Conditions

Conditions	Yield
In methanol at 45℃;	100%

: 58-86-6
D-xylose

: 100-46-9
benzylamine

: 108942-11-6
C12H17NO4

Conditions

Conditions	Yield
In methanol at 45℃;	100%

: 58-86-6
D-xylose

: 131233-91-5
methyl α-D-lyxopyranoside

Conditions

Conditions	Yield
With hydrogenchloride; methanol In water at 68℃; for 1.5h;	100%

: 58-86-6
D-xylose

: 52-90-4
L-Cysteine

: C8H14NO6S(1-)*Na(1+)

Conditions

Conditions	Yield
With sodium hydroxide at 80℃; pH=9.5; Temperature; Flow reactor;	100%

: 75-77-4
chloro-trimethyl-silane

: 58-86-6
D-xylose

: 14251-20-8, 18622-98-5, 18623-23-9, 18623-24-0, 18623-27-3, 18771-81-8, 20585-61-9, 32166-72-6, 32166-73-7, 55555-45-8, 56271-64-8, 56271-65-9, 56271-66-0, 56271-67-1, 56271-70-6, 94942-10-6
1,2,3,4-tetra-O-trimethylsilyl-D-xylopyranose

Conditions

Conditions	Yield
With pyridine at 20℃; for 4h; Inert atmosphere;	100%

: 58-86-6
D-xylose

: 52387-25-4
D-Xylononitrile

Conditions

Conditions	Yield
With phenoxyamine hydrochloride In aq. phosphate buffer; water-d2 at 20℃; for 12h;	98%

: 58-86-6
D-xylose

: 67-64-1
acetone

: 20031-21-4
1,2-O-isopropylidene-α-D-xylose

Conditions

Conditions	Yield
Stage #1: D-xylose; acetone With sulfuric acid Stage #2: With hydrogenchloride In water	97%
Stage #1: D-xylose; acetone With sulfuric acid; copper(II) sulfate at 25℃; Stage #2: With hydrogenchloride In water

: 58-86-6
D-xylose

: 98-01-1
furfural

Conditions

Conditions	Yield
With sulfonated graphitic carbon nitride In water at 100℃; for 0.5h; Solvent; Temperature;	96%
With Sulfonated graphene at 150℃; for 0.666667h; Temperature; Sealed tube;	96%
With hydrogenchloride; 5-methyl-dihydro-furan-2-one In water at 224.84℃; under 28443.9 Torr; for 0.0375h; Kinetics; Temperature; Reagent/catalyst; Concentration; Flow reactor;	93%

: 58-86-6
D-xylose

: 3171-45-7
4,5-dimethyl-1,2-phenylenediamine

: (1'S,2'R,3'R)-5,6-dimethyl-2-[1',2',3',4'-tetrahydroxybutyl]-1H-benzimidazole

Conditions

Conditions	Yield
With iodine In water; acetic acid at 20℃; for 5h;	96%
With iodine; acetic acid In methanol at 20℃; for 13h;

: 58-86-6
D-xylose

: 71292-81-4
2-(4-chlorophenyl)-2-hydroxy-1-phenylethanone

: 1213264-77-7
(6R,7S,8S)-2-(4-chlorophenyl)-3-phenyl-5,6,7,8-tetrahydroimidazo[1,2-a]pyridine-6,7,8-triol

Conditions

Conditions	Yield
With ammonium acetate; oxalic acid at 80℃; for 0.15h; Microwave irradiation; Neat (no solvent);	96%

: 58-86-6
D-xylose

: 119-53-9
2-hydroxy-2-phenylacetophenone

: 1213264-75-5
(6R,7S,8S)-2,3-diphenyl-5,6,7,8-tetrahydroimidazo[1,2-a]pyridine-6,7,8-triol

Conditions

Conditions	Yield
With ammonium acetate; oxalic acid at 80℃; for 0.183333h; Microwave irradiation; Neat (no solvent);	95%

: 58-86-6
D-xylose

: 109-76-2
Trimethylenediamine

: (1S,2R,3R)-1-(Hexahydro-pyrimidin-2-yl)-butane-1,2,3,4-tetraol

Conditions

Conditions	Yield
for 48h;	94%

: 58-86-6
D-xylose

: 86302-43-4
(tert-Butoxycarbonylmethylene)triphenylphosphorane

: 352462-28-3
tert-butyl (E)-2,3-dideoxy-D-xylo-hept-2-enonate

Conditions

Conditions	Yield
In 1,4-dioxane Wittig reaction; Heating;	94%

: 58-86-6
D-xylose

: 1197040-29-1
phenyl isocyanate

: 14401-51-5
4-chlorobenzamidine hydrochloride

: 1268853-91-3
2-(4-chlorophenyl)-5-(hydroxymethyl)-4-phenyl-4,5,6,7-tetrahydro-3H-imidazo[4,5-b]pyridine-6,7-diol

Conditions

Conditions	Yield
With sodium acetate at 90℃; for 0.233333h; Ugi reaction; Microwave irradiation; neat (no solvent);	94%

...Expand

: 58-86-6
D-xylose

: 95-83-0
4-Chloro-1,2-phenylenediamine

: 1609208-15-2
(1S,2R,3R)-2-(1,2,3,4-tetrahydroxybutyl)-1H-6-chlorobenzimidazole

Conditions

Conditions	Yield
With iodine In water; acetic acid at 20℃; for 4h;	94%

: 58-86-6
D-xylose

: 7721-50-8
D-ribulose 1-phosphate

Conditions

Conditions	Yield
With Thermotoga maritima MSB8 L-rhamnulose kinase; Escherichia coli D-xylose isomerase; Pseudomonas Sp, ST-24 D-tagatose 3-epimerase; ATP; sodium hydroxide pH=7.5; Enzymatic reaction;	94%
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;

: 1199-01-5
2-phenylazlactone

: 58-86-6
D-xylose

: 62-53-3
aniline

: C20H20N2O5

Conditions

Conditions	Yield
With 1-butyl-3-methylimidazolium hydroxide; iodine at 20℃; for 4h; Reagent/catalyst; diastereoselective reaction;	94%

...Expand

: 58-86-6
D-xylose

: 1111-78-0
ammonium carbamate

: (2R,3R,4S,5R)-2-Amino-tetrahydro-pyran-3,4,5-triol; compound with carbamic acid

Conditions

Conditions	Yield
With ammonium hydroxide In methanol at 37℃; for 5h;	93%

: 58-86-6
D-xylose

: 106-95-6
allyl bromide

: 868159-53-9
(2R,3S,4S)-1,2,3,4,5-pentahydroxyoct-7-ene

Conditions

Conditions	Yield
With indium In water for 10h; Barbier reaction;	93%

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

: 58-86-6
D-xylose

: C12H18N4O7

Conditions

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

D(+)-Xylose Chemical Properties

Molecular Formula: C₅H₁₀O₅
Molecular Weight: 150.13
EINECS: 200-400-7
Index of Refraction: 1.646
Molar Refractivity: 31.02 cm³
Molar Volume: 85.4 cm³
Surface Tension: 75.3 dyne/cm
Density: 1.757 g/cm³
Flash Point: 155.3 °C
Enthalpy of Vaporization: 66.74 kJ/mol
Boiling Point: 333.2 °C at 760 mmHg
Vapour Pressure: 9.92E-06 mmHg at 25 °C
Melting point: 154-158 °C(lit.)
Storage tempreture: Store at RT.
Water solubility: 1 M at 20 °C, clear, colorless
Solubility: Soluble in water
Appearance: White crystals or powder
Structure of (D)-Xylose (CAS NO.58-86-6):

IUPAC Name: (2S,3R,4S,5R)-Oxane-2,3,4,5-tetrol
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+/m1/s1
InChIKey: SRBFZHDQGSBBOR-LECHCGJUSA-N
Product Category of (D)-Xylose (CAS NO.58-86-6): Basic Sugars (Mono & Oligosaccharides);Biochemistry;Xylose;Sweeteners;Carbohydrate Synthesis;Alphabetic;Food & Beverage Standards;CarbohydrateMetabolomics;Metabolic Libraries;Metabolic Pathways;Metabolites and Cofactors on the Metabolic Pathways Chart

D(+)-Xylose Uses

(D)-Xylose (CAS NO.58-86-6) is mainly used to prepare xylitol, and is also widely used in food processing andpharmaceutical industry. It can be used in food and beverage as a non-calorie sweetener, and it used for obesity and diabetes.

D(+)-Xylose Toxicity Data With Reference

Organism	Test Type	Route	Reported Dose (Normalized Dose)	Effect	Source
mouse	LD50	intravenous	11300mg/kg (11300mg/kg)		Yakkyoku. Pharmacy. Vol. 32, Pg. 1367, 1981.
mouse	LD50	oral	23gm/kg (23000mg/kg)		Yakkyoku. Pharmacy. Vol. 32, Pg. 1367, 1981.

D(+)-Xylose Consensus Reports

(D)-XYLOSE is reported in EPA TSCA Inventory.

D(+)-Xylose Safety Profile

Hazard Codes: Irritant Xi
Risk Statements: 36/37/38
R36/37/38:Irritating to eyes, respiratory system and skin.
Safety Statements: 24/25-36-26
S24/25:Avoid contact with skin and eyes.
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36:Wear suitable protective clothing.
WGK Germany: 2
RTECS: ZF2285000
F: 3
Hazard Note: Irritant
HS Code: 29400090
Hazardous Substances Data: 58-86-6(Hazardous Substances Data)
Slightly toxic by ingestion and intravenous routes. When heated to decomposition it emits acrid smoke and irritating vapors.

D(+)-Xylose Specification

(D)-Xylose , its cas register number is 58-86-6. It also can be called D(+)-Xylose ; Wood sugar ; and Xylose . It is hazardous, so the first aid measures and others should be known. Such as: When on the skin: first, should flush skin with plenty of water immediately for at least 15 minutes while removing contaminated clothing. Secondly, get medical aid. Or in the eyes: Flush eyes with plenty of water for at least 15 minutes, occasionally lifting the upper and lower eyelids. Then get medical aid soon. While, it's inhaled: Remove from exposure and move to fresh air immediately. And as soon as to get medical aid. Then you have the ingesting of the product: Wash mouth out with water, and get medical aid immediately. Notes to physician: Treat supportively and symptomatically.
In addition, (D)-Xylose (CAS NO.58-86-6) could be stable under normal temperatures and pressures. It is not compatible with strong oxidizing agents, and you must not take it with incompatible materials, dust generation. And also prevent it to broken down into hazardous decomposition products: Carbon monoxide, carbon dioxide.

Product Name

D(+)-Xylose

Synthetic route

D(+)-Xylose Chemical Properties

D(+)-Xylose Uses

D(+)-Xylose Toxicity Data With Reference

D(+)-Xylose Consensus Reports

D(+)-Xylose Safety Profile

D(+)-Xylose Specification

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