Glycyl-glycyl-glycine supplier

Name
Glycyl-glycyl-glycine
EINECS 209-122-0
CAS No. 556-33-2
Article Data39
CAS DataBase
Density 1.373 g/cm³
Solubility H₂O: 0.5 M at 20 °C, clear, colorless
Melting Point 240-250 °C
Formula C₆H₁₁N₃O₄
Boiling Point 638.8 °C at 760 mmHg
Molecular Weight 189.171
Flash Point 340.1 °C
Transport Information
Appearance white crystalline powder
Safety
Risk Codes
Molecular Structure
Hazard Symbols
Synonyms Glycylglycylglycine;gly-l-gly-l-gly;N-(N-Glycylglycyl)glycine;
PSA 121.52000
LogP -1.25580

Synthetic route

: 15028-44-1
DL-phenylalanine methyl ester

: 75719-94-7
1-O-(glycylglycylglycyl)-β-D-glucopyranose

A: 556-33-2
glycine-glycine-glycine

B: 84814-47-1
glycylglycylglycyl-D,L-phenylalanine methyl ester

Conditions

Conditions	Yield
With 4-methyl-morpholine In N,N-dimethyl-formamide at 38℃; for 72h;	A 67% B 92%
With 4-methyl-morpholine In N,N-dimethyl-formamide at 38℃; for 72h;	A 67% B 28%

...Expand

: 2566-20-3
[2-(2-Benzyloxycarbonylamino-acetylamino)-acetylamino]-acetic acid

: 556-33-2
glycine-glycine-glycine

Conditions

Conditions	Yield
With acetic acid In methanol Ambient temperature; electrolysis: palladium/graphite cathode, -0.6 V to -1.0 V SCE, current density = 15 mA/cm2, catholyte: NaClO4;	90%
With cell extract of Sphingomonas paucimobilis SC 16113 In water at 42℃; for 20h; Enzymatic reaction;	23 % Chromat.

: tetrabutylphosphonium glycinate

: 5680-79-5
glycine ethyl ester hydrochloride

: 556-33-2
glycine-glycine-glycine

Conditions

Conditions	Yield
Stage #1: tetrabutylphosphonium glycinate for 3h; Inert atmosphere; Stage #2: glycine ethyl ester hydrochloride In chloroform at 60℃; for 24h; Stage #3: With acetic acid In chloroform at 20℃; for 10h;	66%

: 56-40-6
glycine

A: 556-33-2
glycine-glycine-glycine

B: 7365-83-5
N-carbamoylmethyl-glycine

C: 598-41-4
H-Gly-NH2

Conditions

Conditions	Yield
With 1,2,4-Triazole; Sodium trimetaphosphate; magnesium chloride In water for 20h; Ambient temperature; var.reag.: pyrrole, pyrrolidine, pyrrazole, imidazole, tetrazole, adenine,quanine, thyamine, uracile, adenosine, quanosine,thymidine, uridine and add of MgCl2: var. pH, time and temp.;	A 5.5% B 23.6% C 3.2%

...Expand

: 15474-96-1
chloroacetyldiglycine

A: 106-57-0
Glycine anhydride

B: 556-33-2
glycine-glycine-glycine

Conditions

Conditions	Yield
With ammonia; water at 25℃;

: 27440-17-1
N-carboxy-glycyl=>glycyl=>glycine

: 556-33-2
glycine-glycine-glycine

Conditions

Conditions	Yield
With borax; sodium dihydrogenphosphate at 26℃; Equilibrium constant;

: 75719-95-8
1-O-(glycylglycylglycyl)-β-D-glucopyranose mono-oxalate

A: 492-61-5
β-D-glucose

B: 556-33-2
glycine-glycine-glycine

Conditions

Conditions	Yield
With β-D-glucosidase; nitrate buffer In water at 37℃; for 6h;

: 75719-94-7
1-O-(glycylglycylglycyl)-β-D-glucopyranose

A: 492-61-5
β-D-glucose

B: 556-33-2
glycine-glycine-glycine

Conditions

Conditions	Yield
In water for 96h; decompn. with/without 0.1M HCl;

: 56-40-6
glycine

A: 556-33-2
glycine-glycine-glycine

B: 637-84-3
tetraglycine

C: 7093-67-6
pentaglycine

D: 556-50-3
glycylglycine

Conditions

Conditions	Yield
titanium(IV) oxide In water for 24h; Product distribution; Irradiation; reactions between var. conditions and with var. semiconductor photocatalysts with and without platinization;	A 0.00021 mmol B 0.00018 mmol C 0.00010 mmol D 0.01026 mmol

...Expand

: 56-40-6
glycine

A: 556-33-2
glycine-glycine-glycine

B: 556-50-3
glycylglycine

Conditions

Conditions	Yield
With copper dichloride In water at 80 - 90℃; Mechanism; Product distribution; Rate constant; other alkali and alkaline-earth-metal cations;
Cu(2+)-doted montmorillonite In water at 80℃; Product distribution; evaporation during 24 h, 4-5 cycles; also by constant volume; natural montmorillonite as catalyst, diglycine as substrate, other products;

: 56-40-6
glycine

A: 556-33-2
glycine-glycine-glycine

B: 556-50-3
glycylglycine

C: aminoacetyl phosphate

D: 67278-70-0
N-(carboxymethyl)phophoroamidate

Conditions

Conditions	Yield
With sodium hydroxide; Sodium trimetaphosphate In water for 96h; Product distribution; Ambient temperature; variation of mixing ratio of the starting materials, pH, reaction time;	A n/a B n/a C 25.3 % Chromat. D 22.7 % Chromat.
With sodium hydroxide; Sodium trimetaphosphate In water for 96h; Ambient temperature; pH=12;	A n/a B n/a C 25.3 % Chromat. D 22.7 % Chromat.

...Expand

: 15474-96-1
chloroacetyldiglycine

: ammonium hydroxide

: 556-33-2
glycine-glycine-glycine

Conditions

Conditions	Yield
at 100℃;

<dl-leucyl>-diglycyl-glycine: <dl-leucyl>-diglycyl-glycine

: 556-33-2
glycine-glycine-glycine

Conditions

Conditions	Yield
mit Hefe-Polypeptidase bei pH 7.0;

N,N-dibenzyl-glycyl->glycyl->glycine: N,N-dibenzyl-glycyl->glycyl->glycine

: 556-33-2
glycine-glycine-glycine

Conditions

Conditions	Yield
With palladium; acetic acid at 80℃; Hydrogenation;

N,N-phthaloyl-glycyl->glycyl->glycine: N,N-phthaloyl-glycyl->glycyl->glycine

: 556-33-2
glycine-glycine-glycine

Conditions

Conditions	Yield
With ethanol; hydrazine hydrate

N-<(2-nitro-phenoxy)-acetyl>-glycyl->glycyl->glycine: N-<(2-nitro-phenoxy)-acetyl>-glycyl->glycyl->glycine

: 556-33-2
glycine-glycine-glycine

Conditions

Conditions	Yield
With sodium hydrogencarbonate; platinum Hydrogenation.Erhitzen des Reaktionsprodukts mit H2O;

N-benzyloxycarbonyl-glycyl->glycyl->glycine benzyl ester: N-benzyloxycarbonyl-glycyl->glycyl->glycine benzyl ester

: 556-33-2
glycine-glycine-glycine

Conditions

Conditions	Yield
With hydrogen bromide; acetic acid

N-benzyloxycarbonyl-glycyl->glycyl->glycine: N-benzyloxycarbonyl-glycyl->glycyl->glycine

: 556-33-2
glycine-glycine-glycine

Conditions

Conditions	Yield
With hydrogen bromide; acetic acid

N-chloroacetyl-glycyl->glycyl->glycine: N-chloroacetyl-glycyl->glycyl->glycine

: 556-33-2
glycine-glycine-glycine

Conditions

Conditions	Yield
With lithium hydroxide; water; 1,2-diamino-benzene

N-trifluoroacetyl-glycyl->glycyl->glycine ethyl ester: N-trifluoroacetyl-glycyl->glycyl->glycine ethyl ester

: 556-33-2
glycine-glycine-glycine

Conditions

Conditions	Yield
With barium dihydroxide

: 91881-03-7
leucyl=>glycyl=>glycyl=>glycine

: furan-2,3,5(4H)-trione pyridine (1:1)

yeastpolypeptidase: yeastpolypeptidase

A: 556-33-2
glycine-glycine-glycine

B: 328-39-2
LEUCINE

C d-leucyl-diglycyl-glycine: d-leucyl-diglycyl-glycine

Conditions

Conditions	Yield
dl-leucyl-diglycyl-glycine;

...Expand

: 7770-50-5
N-benzyloxycarbonylglycylglycylglycylglycine

papain-substances: papain-substances

A: 556-33-2
glycine-glycine-glycine

B: 1138-80-3
N-(Benzyloxycarbonyl)glycine

Conditions

Conditions	Yield
Hydrolysis;

...Expand

: 56-40-6
glycine

A: 106-57-0
Glycine anhydride

B: 556-33-2
glycine-glycine-glycine

C: 637-84-3
tetraglycine

D: 556-50-3
glycylglycine

Conditions

Conditions	Yield
With hydrogen In water at 200℃; under 187515 Torr; for 0.0333333h; Product distribution; Further Variations:; Temperatures; Reagents;

...Expand

: 637-84-3
tetraglycine

A: 556-33-2
glycine-glycine-glycine

B: 56-40-6
glycine

Conditions

Conditions	Yield
With deuteriated sodium hydroxide; dihydrogen peroxide; water-d2 at 37℃; Kinetics;

: 106-57-0
Glycine anhydride

: 56-40-6
glycine

A: 556-33-2
glycine-glycine-glycine

B: 556-50-3
glycylglycine

Conditions

Conditions	Yield
With water at 200℃; under 187515 Torr; pH=5.9; Kinetics;

...Expand

: 556-50-3
glycylglycine

: 56-40-6
glycine

A: 106-57-0
Glycine anhydride

B: 556-33-2
glycine-glycine-glycine

Conditions

Conditions	Yield
In water at 200℃; under 187515 Torr; pH=5.7; Kinetics;

...Expand

: 28320-73-2
((N-(tert-butoxycarbonyl)glycyl)glycyl)glycine

: 556-33-2
glycine-glycine-glycine

Conditions

Conditions	Yield
With trifluoroacetic acid at 20℃; for 2h;

: 29022-11-5
N-(fluoren-9-ylmethoxycarbonyl)glycine

: 556-33-2
glycine-glycine-glycine

Conditions

Conditions	Yield
Multistep reaction.;

: γ-Glu-Gly-Gly-Gly

A: 556-33-2
glycine-glycine-glycine

B: 56-86-0
L-glutamic acid

Conditions

Conditions	Yield
With recombinant Pseudomonas nitroreducens IFO12694 γ-glutamyltranspeptidase at 30℃; for 0.0333333h; pH=10.5; aq. buffer; Enzymatic reaction;

: 556-33-2
glycine-glycine-glycine

: 28920-43-6
(fluorenylmethoxy)carbonyl chloride

: 9-fluorenylmethoxycarbonyl Gly-Gly-Gly-OH

Conditions

Conditions	Yield
With sodium carbonate In tetrahydrofuran at 0 - 20℃; for 4h;	100%

: 556-33-2
glycine-glycine-glycine

: 104-15-4
toluene-4-sulfonic acid

: 100-49-2
cyclohexylmethyl alcohol

: [2-(2-amino-acetylamino)-acetylamino]-acetic acid cyclohexylmethyl ester; compound with toluene-4-sulfonic acid

Conditions

Conditions	Yield
In toluene for 3h; Heating;	99%

...Expand

: 556-33-2
glycine-glycine-glycine

: 24424-99-5
di-tert-butyl dicarbonate

: 28320-73-2
((N-(tert-butoxycarbonyl)glycyl)glycyl)glycine

Conditions

Conditions	Yield
With sodium hydrogencarbonate In N,N-dimethyl-formamide at 0 - 20℃; for 30h;	98%
With sodium hydrogencarbonate In water; N,N-dimethyl-formamide at 20℃; for 1h;	96%
With guanidine hydrochloride In ethanol at 35 - 40℃; for 10h;	91%

: 50-00-0
formaldehyd

: 556-33-2
glycine-glycine-glycine

: N,N-dimethyl-glycyl=>glycyl=>glycine

Conditions

Conditions	Yield
With palladium 10% on activated carbon; hydrogen In water under 3000.3 Torr; for 4h;	98%

: 556-33-2
glycine-glycine-glycine

: 124455-85-2
Mal-Tyr-OMe

: 132402-94-9
Mal-Tyr-Gly-Gly-Gly-OH

Conditions

Conditions	Yield
With sodium hydroxide at -13℃; for 5h; α-chymotrypsin; in ice;	91.2%

: 556-33-2
glycine-glycine-glycine

: 82655-59-2
N-[(diethylamino)carbonothioyl]benzenecarboximidoyl chloride

: C18H24N5O4S(1-)*K(1+)

Conditions

Conditions	Yield
With potassium hydroxide In ethanol at 20℃; for 8h;	90%

: 556-33-2
glycine-glycine-glycine

: 111-70-6
n-heptan1ol

: 104-15-4
toluene-4-sulfonic acid

: TsOH*GGG-OC7H15

Conditions

Conditions	Yield
In toluene Heating;	89%
In toluene Reflux; Dean-Stark;	89%

...Expand

: 556-33-2
glycine-glycine-glycine

: 77374-43-7
Z-Cys(BzlOMe)-ONSu

: 77374-44-8
Z-Cys(BzlOMe)-Gly3-OH

Conditions

Conditions	Yield
With sodium hydrogencarbonate In 1,4-dioxane; water for 24h; Ambient temperature;	85%

: 556-33-2
glycine-glycine-glycine

: 6780-38-7
N-phthaloylglycine chloride

: (2-{2-[2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-acetylamino]-acetylamino}-acetylamino)-acetic acid

Conditions

Conditions	Yield
Stage #1: glycine-glycine-glycine With magnesium oxide In water at 25℃; for 4h; Stage #2: N-phthaloylglycine chloride In 1,4-dioxane; water at 25℃; for 2h;	85%

: 3401-57-8
N-benzyloxycarbonyl-S-benzyl-L-cysteine succinimido-ester

: 556-33-2
glycine-glycine-glycine

: 32979-23-0
Z-Cys(Bzl)-Gly3-OH

Conditions

Conditions	Yield
With sodium hydrogencarbonate In 1,4-dioxane for 24h; Ambient temperature;	84%

: 556-33-2
glycine-glycine-glycine

: 64-17-5
ethanol

: 16194-06-2
glycyl-glycyl-glycine ethyl ester hydrochloride

Conditions

Conditions	Yield
With thionyl chloride for 4h; Heating;	83%
With hydrogenchloride for 72h;	52.9%

: 556-33-2
glycine-glycine-glycine

: 64-17-5
ethanol

: 104-15-4
toluene-4-sulfonic acid

: glycylglycylglycine ethyl ester p-toluenensulfonate

Conditions

Conditions	Yield
In toluene for 96h; Heating;	83%
for 4h; Heating;	72.2%

...Expand

: 556-33-2
glycine-glycine-glycine

: 90236-37-6
succinimidyl-S-benzoylthioglycolate

: 103725-47-9
benzoylmercaptoacetylglycylglycylglycine

Conditions

Conditions	Yield
With sodium hydroxide In acetonitrile at 20 - 60℃; for 6h;	82%
With sodium hydroxide In water for 2.5h; Heating;

: 556-33-2
glycine-glycine-glycine

: 1610596-19-4
(9H-fluoren-9-yl)methyl 1,2-dimethyl-2-((1-(3-oxo-3-(perfluorophenoxy)propyl)-1H-indol-2-yl)methyl)hydrazine-1-carboxylate

: 2-(2-(2-(3-(2-((2-(((9H-fluoren-9-yl)methoxy)carbonyl)-1,2-dimethylhydrazinyl)methyl)-1H-indol-1-yl)propanamido)acetamido)acetamido)acetic acid

Conditions

Conditions	Yield
With sodium hydrogencarbonate In N,N-dimethyl acetamide; water; acetonitrile at 20℃; for 22h;	82%

: 556-33-2
glycine-glycine-glycine

: 82655-60-5
[(morpholinyl)(thiocarbonyl)]benzimidoyl chloride

: C18H22N5O5S(1-)*K(1+)

Conditions

Conditions	Yield
With potassium hydroxide In ethanol at 20℃; for 8h;	82%

: 556-33-2
glycine-glycine-glycine

: 639-58-7
triphenyltin chloride

: (C6H5)2Sn[H2NCH2C(O)NHCH2C(O)NCH2C(O)O]*CH3OH

Conditions

Conditions	Yield
With sodium; methanol In methanol byproducts: NaCl; N2; dissolving sodium in dry methanol, addn. of this soln. to methanolicsoln. of triglycine, refluxing with stirring for 3-4 h, addn. of methan olic soln. of triphenyltin(IV) chloride, refluxing with stirring for 6-7h; filtration of the centrifuged mixt., solvent removal under reduced pressure, trituration with hexane or petroleum ether, recrystn. from methanol-hexane or methanol-petroleum ether; elem. anal.;	80%

Yield

With sodium; methanol In methanol byproducts: NaCl; N2; dissolving sodium in dry methanol, addn. of this soln. to methanolicsoln. of triglycine, refluxing with stirring for 3-4 h, addn. of methan olic soln. of triphenyltin(IV) chloride, refluxing with stirring for 6-7h; filtration of the centrifuged mixt., solvent removal under reduced pressure, trituration with hexane or petroleum ether, recrystn. from methanol-hexane or methanol-petroleum ether; elem. anal.;

80%

: 109-99-9
tetrahydrofuran

: 556-33-2
glycine-glycine-glycine

: 951212-15-0
[MoCl(η3-methylallyl)(CO)2(κ2(N,O)-pyridine-2-carboxaldehyde)]

: 1359977-81-3
[MoCl(η3-methallyl)(CO)2(NC5H4-2-C(H)=NCH2CONHCH2CONHCH2COOH)]*THF

Conditions

Conditions	Yield
In tetrahydrofuran; methanol (N2); Schlenk technique; mixt. of Mo complex and peptide in THF/MeOH wasrefluxed for 7 h; evapd. (vac.); washed (CH2Cl2); extd. (THF); filtered through kieselguhr; hexane slowly diffused into concd. THF soln. at -20°C; elem. anal.;	78%

...Expand

: 556-33-2
glycine-glycine-glycine

: 543-20-4
succinoyl dichloride

: 103499-98-5
succinyl bis

Conditions

Conditions	Yield
With sodium hydroxide In acetone for 0.5h;	77%

: 556-33-2
glycine-glycine-glycine

: 104-15-4
toluene-4-sulfonic acid

: 100-51-6
benzyl alcohol

: triglycine benzyl ester toluenesulfonic acid salt

Conditions

Conditions	Yield
In toluene Heating;	77%
In toluene for 8h; Heating;	77%

...Expand

: 10025-99-7
potassium tetrachloroplatinate(II)

: 556-33-2
glycine-glycine-glycine

: 222528-78-1
cis-dichloro-bis(glycylglycylclycine)platinum(II)

Conditions

Conditions	Yield
In potassium hydroxide Gly-Gly-Gly and K2PtCl4 stirred in aq. KOH for 3 d at room temp.; evapd.in vac.; dissolved in aq. HCl; evapd.; dissolved in DMF and filtered; a dded dropwise to acetone/Et2O; repeated pptn. from DMF/acetone with Et2O; centrifuged; washed with Et2O; dried over P2O5 in vac.; elem. anal.;	77%

: 67-56-1
methanol

: 556-33-2
glycine-glycine-glycine

: 39692-67-6
methyl 2-(2-(2-aminoacetamido)acetamido)acetate hydrochloride

Conditions

Conditions	Yield
With hydrogenchloride for 3h; Heating;	76%
With hydrogenchloride

: 37366-09-9
dichloro(benzene)ruthenium(II) dimer

: 556-33-2
glycine-glycine-glycine

: 128092-00-2
{(η6-C6H6)Ru(NH2CH2CONCH2CONHCH2CO2H)Cl}

Conditions

Conditions	Yield
In water dissolving Ru-compd. in water by heating, filtration, addn of triglycine; redn. of vol. to 1 ml, crystn. by addn. of methanol and cooling to o°C; elem. anal.;	76%

: 556-33-2
glycine-glycine-glycine

: (2-ethoxy-ethylsulfanyl)-acetic acid 2,5-dioxo-pyrrolidin-1-yl ester

: (2-{2-[2-(2-ethoxy-ethylsulfanyl)-acetylamino]-acetylamino}-acetylamino)-acetic acid

Conditions

Conditions	Yield
With sodium hydrogencarbonate In water; acetonitrile	75.4%

: 556-33-2
glycine-glycine-glycine

: 154715-61-4
4-uulfamoyl-benzoic acid 2,5-dioxo-pyrrolidin-1-yl ester

: 165682-40-6
1-<((glycylglycyl)glycyl)carbonyl>-4-sulfamoylbenzene

Conditions

Conditions	Yield
With potassium dihydrogenphosphate In acetone for 2h; Ambient temperature;	75%
In acetone at 20℃; for 2h; pH=7.0 - 7.5;

: 556-33-2
glycine-glycine-glycine

: 818-08-6
di(n-butyl)tin oxide

: (C4H9)2Sn[H2NCH2C(O)NHCH2C(O)NCH2C(O)O]

Conditions

Conditions	Yield
In methanol N2; dropwise addn. of a dry hot methanolic soln. of tin compd. to hot methanolic soln. of triglycine (1:1 mol. ratio), refluxing with stirring for 14-16 h with azeotropic removal of water; filtration, solvent removal under reduced pressure, crystn. by trituration with hexane, recrystn. from methanol-hexane; elem. anal.;	75%

: 109-99-9
tetrahydrofuran

: 556-33-2
glycine-glycine-glycine

: [ReBr(CO)3(pyridine-2-carboxaldehyde)]

: fac-[ReBr(CO)3(NC5H4-2-C(H)=NCH2CONHCH2CONHCH2COOH)]*THF

Conditions

Conditions	Yield
In ethanol (N2); Schlenk technique; mixt. of Re complex and peptide in EtOH was refluxed for 2 h; evapd. (vac.); washed (hexane, CH2Cl2/hexane, 1/1); dissolved in THF; filtered through kieselguhr; hexane added; evapd. (vac.); elem. anal.;	75%

...Expand

: 109-99-9
tetrahydrofuran

: 556-33-2
glycine-glycine-glycine

: [MnBr(CO)3(pyridine-2-carboxaldehyde)]

: fac-[MnBr(CO)3(NC5H4-2-C(H)=NCH2CONHCH2CONHCH2COOH)]*THF

Conditions

Conditions	Yield
In ethanol (N2); Schlenk technique; mixt. of Mn complex and peptide in EtOH was refluxed for 9 h; evapd. (vac.); washed (hexane, CH2Cl2/hexane, 1/1); dissolved in THF/MeOH; filtered through kieselguhr; hexane added; evapd. (vac.); elem. anal.;	73%

...Expand

: 556-33-2
glycine-glycine-glycine

: 920-46-7
Methacryloyl chloride

: 61435-67-4
N-Methacryloyldiglycylglycin

Conditions

Conditions	Yield
Stage #1: glycine-glycine-glycine With sodium hydroxide In water at 0 - 5℃; pH=9 - 10.5; ice salt bath; Stage #2: Methacryloyl chloride In water at 0 - 20℃; pH=9 - 10.5; Stage #3: With nitric acid In water	73%

Glycyl-glycyl-glycine Specification

The Glycine, glycylglycyl-, with CAS registry number 556-33-2, belongs to the following product categories: (1)Biochemistry; (2)Oligopeptides; (3)Peptide Synthesis. It has the systematic name of glycylglycylglycine. This chemical is a kind of white crystalline powder. And it should be stored at the temperature of 2-8°C. What's more, its EINECS is 209-122-0.

Physical properties of Glycine, glycylglycyl-: (1)ACD/LogP: -2.04; (2)# of Rule of 5 Violations: 1; (3)ACD/LogD (pH 5.5): -4.53; (4)ACD/LogD (pH 7.4): -5.02; (5)ACD/BCF (pH 5.5): 1; (6)ACD/BCF (pH 7.4): 1; (7)ACD/KOC (pH 5.5): 1; (8)ACD/KOC (pH 7.4): 1; (9)#H bond acceptors: 7; (10)#H bond donors: 5; (11)#Freely Rotating Bonds: 6; (12)Polar Surface Area: 70.16 Å²; (13)Index of Refraction: 1.524; (14)Molar Refractivity: 42.19 cm³; (15)Molar Volume: 137.7 cm³; (16)Polarizability: 16.72×10^-24cm³; (17)Surface Tension: 62.7 dyne/cm; (18)Density: 1.373 g/cm³; (19)Flash Point: 340.1 °C; (20)Enthalpy of Vaporization: 102.93 kJ/mol; (21)Boiling Point: 638.8 °C at 760 mmHg; (22)Vapour Pressure: 5.82E-18 mmHg at 25°C.

You can still convert the following datas into molecular structure:
(1)SMILES: O=C(NCC(=O)O)CNC(=O)CN
(2)InChI: InChI=1/C6H11N3O4/c7-1-4(10)8-2-5(11)9-3-6(12)13/h1-3,7H2,(H,8,10)(H,9,11)(H,12,13)
(3)InChIKey: XKUKSGPZAADMRA-UHFFFAOYAU
(4)Std. InChI: InChI=1S/C6H11N3O4/c7-1-4(10)8-2-5(11)9-3-6(12)13/h1-3,7H2,(H,8,10)(H,9,11)(H,12,13)
(5)Std. InChIKey: XKUKSGPZAADMRA-UHFFFAOYSA-N

Product Name

Glycyl-glycyl-glycine

Synthetic route

Glycyl-glycyl-glycine Specification

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