Dl-glyceraldehyde supplier

Name
DL-GLYCERALDEHYDE
EINECS
CAS No. 56-82-6
Article Data159
CAS DataBase
Density 1.593 g/cm3 (-5℃)
Solubility 29.13g/L(18 oC)
Melting Point 144-145oC(lit.)
Formula C3H6 O3
Boiling Point 107.25°C (rough estimate)
Molecular Weight 90.0788
Flash Point
Transport Information
Appearance
Safety Mildly toxic by intraperitoneal route. Mutation data reported.
Risk Codes
Molecular Structure
Hazard Symbols
Synonyms Glyceraldehyde,DL- (8CI); Propanal, 2,3-dihydroxy-, (?à)-; (?à)-Glyceraldehyde; 2,3-Dihydroxypropanal; 2,3-Dihydroxypropionaldehyde;DL-Glyceraldehyde; DL-Glyceric aldehyde; Glyceraldehyde; Glyceric aldehyde;Glycerinaldehyde; Glycerose; NSC 67934; dl-Glyceraldehyde; a,b-Dihydroxypropionaldehyde
PSA 57.53000
LogP -1.46150

Synthetic route

: 56-81-5
glycerol

: 56-82-6
Glyceraldehyde

Conditions

Conditions	Yield
With nano-MnO2; graphite at 75℃; for 1.5h; Electrochemical reaction; Ultrasonic;	91.6%
With oxygen In water at 45 - 50℃; for 5h; Reagent/catalyst;	91%
With tert.-butylhydroperoxide; C56H62Cl2Mn2N6O10P2 In water; acetonitrile at 80℃; for 4h; Catalytic behavior; Green chemistry;	44%

: 56-81-5
glycerol

A: 473-81-4
glyceric acid

B: 96-26-4
dihydroxyacetone

C: 56-82-6
Glyceraldehyde

Conditions

Conditions	Yield
With oxygen In water at 60℃; Catalytic behavior; Reagent/catalyst; Autoclave; chemoselective reaction;	A 84.2% B 9.5% C 6.3%
With oxygen In water at 60℃; under 760.051 Torr; for 4h; Catalytic behavior;
With Pt-MCM-41 catalyst; oxygen In water at 69.84℃; under 760.051 Torr; pH=Ca. 7; Kinetics; Catalytic behavior; Reagent/catalyst; Temperature;

...Expand

starch: starch

A: 849585-22-4
LACTIC ACID

B: 56-82-6
Glyceraldehyde

Conditions

Conditions	Yield
With aluminum (III) chloride; tin(ll) chloride In water at 189.84℃; under 22502.3 Torr; for 2h; Catalytic behavior; Inert atmosphere; Autoclave;	A 81% B 5.2%

: 130998-84-4
rac-Glycerinaldehyd-2-phosphat Natriumsalz

A: sodium phosphoenol pyruvaldehyde

B: 56-82-6
Glyceraldehyde

Conditions

Conditions	Yield
In aq. phosphate buffer at 60℃; for 23h; pH=7;	A 74% B 12%

: 56-81-5
glycerol

A: 849585-22-4
LACTIC ACID

B: 96-26-4
dihydroxyacetone

C: 56-82-6
Glyceraldehyde

Conditions

Conditions	Yield
With silver dodecamolybdophosphate; oxygen In water at 60℃; under 3750.38 Torr; for 5h; Catalytic behavior; Reagent/catalyst; Autoclave;	A 72% B n/a C n/a
With phosphomolybdic acid; dihydrogen peroxide at 60℃; for 0.133333h; Catalytic behavior;	A 42% B n/a C n/a
With MoO40W12(3-)*Cr(3+); oxygen In water at 60℃; under 7500.75 Torr; for 20h; Autoclave;	A 12.9% B 8.6% C 5.9%

...Expand

: 67-56-1
methanol

: sucrose

A: 530-26-7
D-Mannose

B: 27871-49-4
(S)-Methyl lactate

C: 1663-35-0
2-methoxyethyl vinyl ether

D: 5837-73-0
methyl 2-hydroxybut-3-enoate

E: 1186-47-6
1,1-dihydroxyacetone

F: 56-82-6
Glyceraldehyde

G: 621-63-6
glycoaldehyde diethyl acetal

Conditions

Conditions	Yield
With potassium carbonate at 160℃; for 16h; Reagent/catalyst; Flow reactor;	A n/a B 72% C n/a D n/a E n/a F n/a G n/a

...Expand

: 765-34-4
Glycidaldehyde

: 4570-45-0
2-amino-1,3-oxazole

A: C6H10N2O4

B: 56-82-6
Glyceraldehyde

Conditions

Conditions	Yield
With hydrogenchloride; sodium hydroxide In water; water-d2 for 59h; pH=5;	A 72% B 10%
With hydrogenchloride; sodium hydroxide In water; water-d2 for 30h; pH=3;	A 17% B 29%

...Expand

: 56-81-5
glycerol

A: 473-81-4
glyceric acid

B: 56-82-6
Glyceraldehyde

Conditions

Conditions	Yield
With perchloric acid In ethanol at 20℃; pH=1; Concentration; Reagent/catalyst; Electrochemical reaction;	A 9% B 70.6%
With Pseudomonas putida HK-5 pyrroloquinoline quinone-dependent alcohol dehydrogenase; 4,4'-azobis(1-methylpyridinium) bis(methyl sulfate); NADH In aq. buffer for 6h; pH=7.1; Catalytic behavior; Time; Electrolysis; Enzymatic reaction;	A 53% B 15%
With silica-supported platinum; oxygen In water at 89.84℃; for 24h;

: 56-81-5
glycerol

A: 64-18-6
formic acid

B: 79-14-1
glycolic Acid

C: 56-82-6
Glyceraldehyde

Conditions

Conditions	Yield
With potassium hydroxide for 4h; Reagent/catalyst; Electrochemical reaction;	A 70% B 13% C 17%
With dihydrogen peroxide In water at 60℃; for 4h;

...Expand

: 50-00-0
formaldehyd

A: 141-46-8
Glycolaldehyde

B: 56-82-6
Glyceraldehyde

Conditions

Conditions	Yield
With triethylamine In N,N-dimethyl-formamide at 120℃; under 15751.6 Torr; for 1h; Temperature; Pressure; Reagent/catalyst; Solvent;	A 63.52% B 23.12%
With triethylamine In N,N-dimethyl-formamide at 100℃; under 3750.38 Torr; for 1h; Temperature; Pressure; Reagent/catalyst; Solvent;	A 25.17% B 38.23%
With 5-methoxy-1,3,4-triphenyl-4,5-dihydro-1H-1,2-4-triazoline In various solvent(s) at 80℃;

: 56-81-5
glycerol

A: 849585-22-4
LACTIC ACID

B: 473-81-4
glyceric acid

C: 96-26-4
dihydroxyacetone

D: 64-19-7
acetic acid

E: 56-82-6
Glyceraldehyde

Conditions

Conditions	Yield
With oxygen In water at 60℃; under 3750.38 Torr; for 5h; Catalytic behavior; Autoclave;	A 45% B n/a C n/a D n/a E n/a

...Expand

: 56-81-5
glycerol

A: 79-14-1
glycolic Acid

B: 849585-22-4
LACTIC ACID

C: 96-26-4
dihydroxyacetone

D: 56-82-6
Glyceraldehyde

Conditions

Conditions	Yield
With dihydrogen peroxide In water at 60℃; for 1h; Reagent/catalyst; Temperature; Time;	A n/a B 36% C n/a D n/a

...Expand

: 50-00-0
formaldehyd

: 56-82-6
Glyceraldehyde

Conditions

Conditions	Yield
With triethylamine In N,N-dimethyl-formamide at 160℃; under 12001.2 Torr; for 1.66667h; Temperature; Pressure; Reagent/catalyst; Solvent;	30.53%

agarose: agarose

A: 67-47-0
5-hydroxymethyl-2-furfuraldehyde

B: 849585-22-4
LACTIC ACID

C: 1186-47-6
1,1-dihydroxyacetone

D: 56-82-6
Glyceraldehyde

Conditions

Conditions	Yield
With zinc(II) chloride at 200℃; for 0.416667h;	A 22.6% B n/a C n/a D n/a

...Expand

: 56-81-5
glycerol

A: 79-14-1
glycolic Acid

B: 473-81-4
glyceric acid

C: 56-82-6
Glyceraldehyde

Conditions

Conditions	Yield
With perchloric acid In ethanol at 20℃; pH=1; Reagent/catalyst; Electrochemical reaction;	A 7% B 7.6% C 20.3%

...Expand

: 56-81-5
glycerol

A: 96-26-4
dihydroxyacetone

B: 56-82-6
Glyceraldehyde

C: 78-98-8
2-oxopropanal

Conditions

Conditions	Yield
With 3H(1+)*MoO40W12(3-); oxygen In water at 60℃; under 7500.75 Torr; for 20h; Autoclave;	A 16% B 14.9% C 8.4%

...Expand

agarose: agarose

A: 67-47-0
5-hydroxymethyl-2-furfuraldehyde

B: 849585-22-4
LACTIC ACID

C: 1186-47-6
1,1-dihydroxyacetone

D: 3128-06-1
5-ketohexanoic acid

E: 56-82-6
Glyceraldehyde

Conditions

Conditions	Yield
With chromium chloride at 200℃; for 0.5h;	A 13% B n/a C n/a D n/a E n/a

...Expand

: 78-98-8
2-oxopropanal

A: 849585-22-4
LACTIC ACID

B: 56-82-6
Glyceraldehyde

Conditions

Conditions	Yield
With tin(ll) chloride In water at 109.84℃; under 22502.3 Torr; for 3h; Catalytic behavior; Inert atmosphere; Autoclave;	A 10% B 9.6%

: 57-48-7
D-Fructose

: 87-79-6
L-sorbose

: 56-82-6
Glyceraldehyde

Conditions

Conditions	Yield
With lead(IV) acetate; acetic acid Erwaermen des Reaktionsprodukts mit wss.Schwefelsaeure;

: 75526-35-1
2-Phenyl-4H-[1,3]dioxin

: 56-82-6
Glyceraldehyde

Conditions

Conditions	Yield
With Perbenzoic acid; chloroform at 0℃; dann bei Raumtemperatur, und Verseifen des Reaktionsprodukts mit verd. Essigsaeure auf dem Wasserbad;

: 10487-05-5
3,3-diethoxypropane-1,2-diol

: 56-82-6
Glyceraldehyde

Conditions

Conditions	Yield
With acetic acid dl-glyceraldehyde;

: 488-16-4, 3909-12-4, 7306-96-9, 10191-35-2, 13752-84-6, 20246-26-8, 20703-66-6
(+/-)-erythronic acid

: 56-82-6
Glyceraldehyde

Conditions

Conditions	Yield
die Reaktion des Kupfersalz.Electrolysis;

: 50-99-7
D-glucose

A: 96-26-4
dihydroxyacetone

B: 56-82-6
Glyceraldehyde

Conditions

Conditions	Yield
With sodium carbonate; sodium sulfite bei der Destillation;
With sodium carbonate; sodium sulfite

: 56-81-5
glycerol

A: 96-26-4
dihydroxyacetone

B: 56-82-6
Glyceraldehyde

Conditions

Conditions	Yield
durch Oxydation;
With sodium decatungstate; oxygen In water at 24.84℃; under 760 Torr; Mechanism; Reagent/catalyst; Irradiation;
With zinc(II) oxide In water at 30℃; Kinetics; UV-irradiation;

: 107-02-8
acrolein

: 56-82-6
Glyceraldehyde

Conditions

Conditions	Yield
With sodium chlorate; osmium(VIII) oxide; water at -8℃; zuletzt bei Raumtemperatur;
With osmium(VIII) oxide; barium chlorate; water at -8℃; zuletzt bei Raumtemperatur;
With osmium(VIII) oxide; sulfuric acid; acetic acid In water at 26.4℃; for 24h;
With thallium(III) sulfate In 1,4-dioxane; sulfuric acid at 17.5℃; Kinetics; Thermodynamic data; Mechanism; other acroleine concentration, other temperature, ΔH(excit), ΔS(excit);
With osmium(VIII) oxide; sulfuric acid; acetic acid In water at 26.4℃; for 24h; Rate constant; Thermodynamic data; Mechanism; no reaction with corresponding saturated organic compound (selectivity);absence and presence of acrylonitrile or acrylamide (no polimerization); negligible effect of added salts; variation of concn. of substrate; activation parameters;

: 53735-98-1
(1S,2S)-1,2-bis[(R)-2,2-dimethyl-1,3-dioxolan-4-yl]ethane-1,2-diol

: 56-82-6
Glyceraldehyde

Conditions

Conditions	Yield
With lead(IV) acetate; benzene Erwaermen des Reaktionsprodukts mit wss.Essigsaeure;

: (S)-2-Amino-4-[(R)-1-(carboxymethyl-carbamoyl)-2-(1,2,3-trihydroxy-propylsulfanyl)-ethylcarbamoyl]-butyric acid

A: 70-18-8
GLUTATHIONE

B: 56-82-6
Glyceraldehyde

Conditions

Conditions	Yield
In water at 25℃; Equilibrium constant;

: 50-00-0
formaldehyd

A: 67-56-1
methanol

B: 64-18-6
formic acid

C: 96-26-4
dihydroxyacetone

D: 141-46-8
Glycolaldehyde

E: 56-82-6
Glyceraldehyde

Conditions

Conditions	Yield
With calcium hydroxide; dihydroxyacetone In water at 50℃; Kinetics; Mechanism; other reaction partner, specific co-catalytic activities for the most important intermediates and products;

...Expand

: 50-00-0
formaldehyd

A: 96-26-4
dihydroxyacetone

B: 56-82-6
Glyceraldehyde

Conditions

Conditions	Yield
With triethylamine; 3-ethylbenzothiazolium bromide In ethanol at 65℃; for 6h; Product distribution; var. of base, solvent;
With triethylamine; 3-ethylbenzothiazolium bromide In ethanol at 65℃; for 6h; Yield given;

: 50-00-0
formaldehyd

A: 470-14-4
DL-dendroketose

: 54-17-1, 492-61-5, 492-62-6, 492-66-0, 530-25-6, 530-26-7, 530-27-8, 530-28-9, 552-76-1, 579-36-2, 643-69-6, 655-45-8, 2280-44-6, 3646-73-9, 7282-78-2, 7282-79-3, 7282-80-6, 7282-81-7, 7282-82-8, 7283-02-5, 7283-08-1, 7283-09-2, 7283-10-5, 7283-11-6, 7296-15-3, 7296-64-2, 7322-31-8, 10257-28-0, 12772-65-5, 12773-29-4, 12773-31-8, 12773-32-9, 12773-33-0, 12773-34-1, 19982-85-5, 28538-24-1, 32445-46-8, 32445-47-9, 32445-51-5, 32445-52-6, 34685-56-8, 34685-57-9, 35810-56-1, 39281-65-7, 39281-66-8, 39281-67-9, 39281-68-0, 39281-69-1, 39392-61-5, 39392-62-6, 39392-63-7, 39392-65-9, 39392-66-0, 39392-69-3, 40825-84-1, 40825-86-3, 40825-87-4, 40825-89-6, 42752-07-8, 42789-83-3, 46032-76-2, 54808-89-8, 66069-07-6, 120442-57-1, 120442-58-2, 120442-59-3, 120442-67-3, 131064-91-0, 131064-92-1, 131065-00-4, 131065-01-5, 131348-38-4
D-mannose

: 532-20-7, 613-83-2, 7261-25-8, 7687-39-0, 13221-22-2, 14795-83-6, 15761-67-8, 20074-49-1, 25545-03-3, 25545-04-4, 32445-75-3, 34436-17-4, 36441-93-7, 36468-53-8, 37110-85-3, 37388-49-1, 38029-69-5, 40461-77-6, 40461-89-0, 41546-19-4, 41546-20-7, 41546-21-8, 41546-26-3, 41546-29-6, 41546-30-9, 41546-31-0, 126872-16-0, 131064-98-7
Arabinose

: 54-17-1, 492-61-5, 492-62-6, 492-66-0, 530-25-6, 530-26-7, 530-27-8, 530-28-9, 552-76-1, 579-36-2, 643-69-6, 655-45-8, 2280-44-6, 3646-73-9, 7282-78-2, 7282-79-3, 7282-80-6, 7282-81-7, 7282-82-8, 7283-02-5, 7283-08-1, 7283-09-2, 7283-10-5, 7283-11-6, 7296-15-3, 7296-64-2, 7322-31-8, 10257-28-0, 12772-65-5, 12773-29-4, 12773-31-8, 12773-32-9, 12773-33-0, 12773-34-1, 19982-85-5, 28538-24-1, 32445-46-8, 32445-47-9, 32445-51-5, 32445-52-6, 34685-56-8, 34685-57-9, 35810-56-1, 39281-65-7, 39281-66-8, 39281-67-9, 39281-68-0, 39281-69-1, 39392-61-5, 39392-62-6, 39392-63-7, 39392-65-9, 39392-66-0, 39392-69-3, 40825-84-1, 40825-86-3, 40825-87-4, 40825-89-6, 42752-07-8, 42789-83-3, 46032-76-2, 54808-89-8, 66069-07-6, 120442-57-1, 120442-58-2, 120442-59-3, 120442-67-3, 131064-91-0, 131064-92-1, 131065-00-4, 131065-01-5, 131348-38-4
glucopyranose

E: 56-82-6
Glyceraldehyde

: Arabinose

Conditions

Conditions	Yield
With calcium hydroxide In water at 50℃; for 0.8h; Kinetics; Mechanism; Product distribution; homogeneous catalysis, other time, temperatures, reagent, conc. Ca(OH)2;	A 9.9 % Chromat. B 2.0 % Chromat. C 7.3 % Chromat. D 10.0 % Chromat. E 2.5 % Chromat. F 3.0 % Chromat.

...Expand

: 56-82-6
Glyceraldehyde

: 473-81-4
glyceric acid

Conditions

Conditions	Yield
With 1 wt% Au/TiO2; oxygen In water at 75℃; under 39547.2 Torr; for 3022h; Time; Flow reactor;	100%
With sodium chlorite; dimethyl sulfoxide In aq. phosphate buffer at 0 - 20℃; pH=4;	93%
With iodine; sodium carbonate

: 67-56-1
methanol

: 56-82-6
Glyceraldehyde

: 547-64-8
methyl lactate

Conditions

Conditions	Yield
With tin containing MWW type β-zeolite In decane at 119.84℃; for 24h; Reagent/catalyst;	99%
With Y-zeolite H-USY-6 In water at 115℃; for 48h; Inert atmosphere;	98%
With Sn(salen) functionalized [OMIm]Br at 160℃; under 15001.5 Torr; for 2h; Inert atmosphere; Autoclave; chemoselective reaction;	91.7%

: 56-82-6
Glyceraldehyde

: 849585-22-4
LACTIC ACID

Conditions

Conditions	Yield
With tin containing MWW type β-zeolite In water at 109.84℃; for 6h; Reagent/catalyst;	96%
With Y-zeolite H-USY-6 In water at 125℃; for 48h; Inert atmosphere;	63%
With oxygen In water at 149.84℃; under 3750.38 Torr; for 1h; Reagent/catalyst;	42%

: 56-82-6
Glyceraldehyde

: 130998-84-4
rac-Glycerinaldehyd-2-phosphat Natriumsalz

Conditions

Conditions	Yield
With diamidophosphate In aq. phosphate buffer at 20℃; for 4h; pH=4;	96%

: 56-82-6
Glyceraldehyde

: 616-30-8, 13552-31-3
3-Amino-1,2-propanediol

Conditions

Conditions	Yield
With ammonia; active charcoal; palladium In water	94.5%
With ammonium hydroxide; hydrogen at 55℃; under 15001.5 Torr; for 6h; Autoclave; Green chemistry;

: 96-26-4
dihydroxyacetone

: 56-82-6
Glyceraldehyde

A: 453-17-8
D-Glyceraldehyde

B: 57-48-7, 87-79-6, 87-81-0, 551-68-8, 3615-39-2, 3615-56-3, 6035-50-3, 7776-48-9, 16354-64-6, 17598-81-1, 17598-82-2, 23140-52-5, 30237-26-4, 65732-90-3, 73952-10-0, 73952-11-1, 139686-85-4
L-fructose

Conditions

Conditions	Yield
With E. coli BL21 (DE3) cells harboring pETDRhaD aldolase; sodium borate buffer In water; toluene at 37℃; for 16h; pH=7.6;	A n/a B 92%

...Expand

: 6000-44-8
sodium glycinate

: 56-82-6
Glyceraldehyde

: Sodium; [2,3-dihydroxy-prop-(E)-ylideneamino]-acetate

Conditions

Conditions	Yield
In methanol at 25℃; for 96h;	91%

: 34693-15-7
fructose 1,6-diphosphate

: 56-82-6
Glyceraldehyde

: Phosphoric acid mono-((3S,4R)-3,4,5,6-tetrahydroxy-2-oxo-hexyl) ester

Conditions

Conditions	Yield
With fructose 1,6-bisphosphate aldolase from S. carnosus; triose phosphate isomerase from rabbit muscle [EC 5.3.1.1] In water at 20℃; Addition; Aldol condensation; Enzymatic reaction;	90%

: 96-50-4
2-thiazolylamine

: 56-82-6
Glyceraldehyde

: C9H12N4O2S2

Conditions

Conditions	Yield
In aq. buffer for 24h; pH=7; Reagent/catalyst;	90%

: 75-77-4
chloro-trimethyl-silane

: 30148-50-6
bis(trimethylsilyl)phosphonite

: 56-82-6
Glyceraldehyde

: 112162-72-8
C21H47O8PSi3

Conditions

Conditions	Yield
With triethylamine In benzene 1.) 40-45 deg C, 15 min; 2.) reflux, 2 h;	88%

...Expand

: 6783-05-7
trans-2-phenylvinylboronic acid

: 103-67-3
benzyl-methyl-amine

: 56-82-6
Glyceraldehyde

: (E)-(2R,3R)-3-(Benzyl-methyl-amino)-5-phenyl-pent-4-ene-1,2-diol

Conditions

Conditions	Yield
In ethanol at 25℃;	87%

...Expand

: 120-72-9
indole

: 56-82-6
Glyceraldehyde

: 4531-83-3
3,3-di(1H-indol-3-yl)propane-1,2-diol

Conditions

Conditions	Yield
With scandium tris(trifluoromethanesulfonate) In water; acetonitrile at 40℃; for 24h;	87%
With Montmorillonite K10 at 20℃; for 0.5h;	80%

: 109-80-8
1.3-propanedithiol

: 56-82-6
Glyceraldehyde

: 86040-12-2
(R)-1-(1,3-Dithian-2-yl)-2-hydroxy-1-ethanol

Conditions

Conditions	Yield
With hydrogenchloride for 2h;	86%

: 13331-23-2
fur-2-ylboronic acid

: 56-82-6
Glyceraldehyde

: 91-00-9
Benzhydrylamine

: (2S,3R)-3-(Benzhydryl-amino)-3-furan-2-yl-propane-1,2-diol

Conditions

Conditions	Yield
In ethanol at 25℃;	86%

...Expand

: 110-91-8
morpholine

: 873-73-4
4-n-chlorophenylacetylene

: 56-82-6
Glyceraldehyde

: C15H16ClNO2

Conditions

Conditions	Yield
With gold(III) tribromide In 2,2,2-trifluoroethanol at 60℃; for 24h;	86%

...Expand

: 536-74-3
phenylacetylene

: 56-82-6
Glyceraldehyde

: 103-49-1
dibenzylamine

: C25H23NO

Conditions

Conditions	Yield
With gold(III) tribromide In 2,2,2-trifluoroethanol at 60℃; for 24h;	86%

...Expand

: 2097-71-4
diallylmercury

: 56-82-6
Glyceraldehyde

: 89534-51-0
[R-(R*,R*)]-5-Hexene-1,2,3-triol

Conditions

Conditions	Yield
In water Ambient temperature;	85%

: 110-91-8
morpholine

: 772-38-3
4-tert-Butylphenylacetylene

: 56-82-6
Glyceraldehyde

: C19H25NO2

Conditions

Conditions	Yield
With gold(III) tribromide In 2,2,2-trifluoroethanol at 60℃; for 24h;	85%

...Expand

: 772-38-3
4-tert-Butylphenylacetylene

: 56-82-6
Glyceraldehyde

: 103-49-1
dibenzylamine

: C29H31NO

Conditions

Conditions	Yield
With gold(III) tribromide In 2,2,2-trifluoroethanol at 60℃; for 24h;	85%

...Expand

: 40307-11-7
1-ethyl-4-ethynylbenzene

: 56-82-6
Glyceraldehyde

: 103-49-1
dibenzylamine

: C27H27NO

Conditions

Conditions	Yield
With gold(III) tribromide In 2,2,2-trifluoroethanol at 60℃; for 24h;	84%

...Expand

: 107-05-1
3-chloroprop-1-ene

: 56-82-6
Glyceraldehyde

: 89534-51-0
[R-(R*,R*)]-5-Hexene-1,2,3-triol

Conditions

Conditions	Yield
With aluminium; tin(ll) chloride In methanol; water; acetic acid at 50 - 53℃; for 5h;	82%

: 106-95-6
allyl bromide

: 56-82-6
Glyceraldehyde

: 89534-51-0
[R-(R*,R*)]-5-Hexene-1,2,3-triol

Conditions

Conditions	Yield
With tin In methanol; water; acetic acid 1.)room temperature, 2 h, 2.)electrolysis, 20 deg C;	81%
With tin In tetrahydrofuran; water Ambient temperature; Irradiation;	55%
With tin In water at 20℃;

: 92-54-6
4-phenyl-1-piperazine

: 536-74-3
phenylacetylene

: 56-82-6
Glyceraldehyde

: C21H22N2O

Conditions

Conditions	Yield
With gold(III) tribromide In 2,2,2-trifluoroethanol at 60℃; for 24h;	81%

...Expand

: 21204-67-1
methyl (triphenylphosphoranylidene)acetate

: 56-82-6
Glyceraldehyde

: 10374-47-7
methyl (E)-4,5-dihydroxy-2-pentenoate

Conditions

Conditions	Yield
In benzene Heating;	80%

: 50277-59-3
2-isopropyl-5-methylcyclohexyl chloroformate

: 56-82-6
Glyceraldehyde

: 94219-44-0
2,5-bis(Menthoxycarbonyloxymethylene)-3,6-bis(menthoxycarbonyloxy)-1,4-dioxane

Conditions

Conditions	Yield
With pyridine In chloroform 1.) 0 deg C, 15 min, 2.) room temperature, 24 h, 3.) 40 deg C, 1.5 h, 4.) 60 deg C, 1 h;;	80%

: 56-82-6
Glyceraldehyde

: 1099-45-2
ethyl (triphenylphosphoranylidene)acetate

: 69010-16-8
ethyl (4RS,2E)-4,5-dihydroxypent-2-enoate

Conditions

Conditions	Yield
In dichloromethane	80%

: 67344-77-8
1-(3-bromophenyl)-N-methylmethanamine

: 536-74-3
phenylacetylene

: 56-82-6
Glyceraldehyde

: C19H18BrNO

Conditions

Conditions	Yield
With gold(III) tribromide In 2,2,2-trifluoroethanol at 60℃; for 24h;	80%

...Expand

Dl-glyceraldehyde Chemical Properties

Molecular Structure of Dl-glyceraldehyde (CAS NO.56-82-6):

IUPAC: 2,3-dihydroxypropanal
Molecular Formula:C₃H₆O₃
Molecular Weight:90.08
EINECS:200-290-0
Density:1.272 g/cm³
Melting Point:144-145^oC(lit.)
Flash Point:106^oC
Boiling Point:228^oC at 760 mmHg
Storage temp.:2-8^oC
Product Categories:Carbohydrate;Metabolic Pathways;Metabolites and Cofactors on the Metabolic Pathways Chart
SMILES:O=C[C@@H](O)CO
InChI:InChI=1/C3H6O3/c4-1-3(6)2-5/h1,3,5-6H,2H2/t3-/m1/s1
InChIKey:MNQZXJOMYWMBOU-GSVOUGTGBZ
Index of Refraction:1.454
Molar Volume:70.7 cm³
Surface Tension:53.3 dyne/cm
Molar Refractivity:19.16 cm³
Enthalpy of Vaporization:54.01 kJ/mol
Vapour Pressure:0.0146 mmHg at 25^oC

Dl-glyceraldehyde Toxicity Data With Reference

1.		mmo-sat 100 µg/plate ABCHA6 47,2461,83
2.		ipr-rat LD50:2 g/kg		JPPMAB Journal of Pharmacy and Pharmacology. 17 (1965),814.

Dl-glyceraldehyde Consensus Reports

Reported in EPA TSCA Inventory.

Dl-glyceraldehyde Safety Profile

Mildly toxic by intraperitoneal route. Mutation data reported.
Safty informations about Dl-glyceraldehyde (CAS NO.56-82-6):
WGK Germany:3
RTECS:MA6475000
F:10-23

Dl-glyceraldehyde Specification

Dl-glyceraldehyde with cas registry number of 56-82-6 is also known as Glyceric aldehyde ; Glyceraldehyde ; Dl-glyceraldehyde ; (+-)-Glyceraldehyd ; 3-Dihydroxy-(+/-)-propana ; Dl-glyceraldehyd ; Dl-glycericaldehyde ; Dl-glyceraldehyde crystalline . It is a compound with the appearance of white crystalline powder. It is soluble in water. Dl-glyceraldehyde is used as an organic synthesis intermediate in synthesis of many useful compounds. It is also used in biochemical research.

Product Name

DL-GLYCERALDEHYDE

Synthetic route

Dl-glyceraldehyde Chemical Properties

Dl-glyceraldehyde Toxicity Data With Reference

Dl-glyceraldehyde Consensus Reports

Dl-glyceraldehyde Safety Profile

Dl-glyceraldehyde Specification

Related Products

Hot Products