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Cas:556-33-2
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inquiryUnique advantages Guaranteed purity High quality & competitive price Quality control Fast feedback Prompt shipment Appearance:White powder Storage:Cool dry place Package:1kg/foill bag;25kg/drum Application:amino a
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inquiryAs a leading manufacturer and supplier of chemicals in China, DayangChem not only supply popular chemicals, but also DayangChem’s R&D center offer custom synthesis according to the contract research and development services for the fine c
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About Product Details Item Specification Test Results Appearance White crystalline powder Conform
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inquiryOur company was built in 2009 with an ISO certificate.In the past 6 years, we have grown up as a famous fine chemicals supplier in China and we had established stable business relationships with Samsung,LG,Merck,Thermo Fisher Scientific and so on.O
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Cas:556-33-2
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Cas:556-33-2
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inquiryProduct Detail Minimum Order Qty. 10 Gram
Cas:556-33-2
Min.Order:10 Gram
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inquiryHenan Wentao Chemical Product Co.,Ltd is Located in Zhengzhou High-tech Development Zone with import and export license, We passed ISO 9001:2008 as well, Henan Wentao has developed more than 1000 compounds, which are widely used in the fields of prod
superior quality Appearance:white crystalline powder Storage:Stored in cool, dry and ventilation place; Away from fire and heat Package:1kg/bag, 1kg/drum or 25kg/drum or as per your request. Application:Used as Pharmaceutical Intermediates Transpo
Product Name Glycyl-glycyl-glycine CAS No 556-33-2 Molecular Formula Molecular Weight
Cas:556-33-2
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inquiryHangzhou KeyingChem Co., Ltd. exported this product to many countries and regions at best price. If you are looking for the material’s manufacturer or supplier in China, KeyingChem is your best choice. Pls contact with us freely for getting det
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Cas:556-33-2
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inquiryadvantage: 1. The best price, satisfactory quality; 2. customers have the right to choose the delivery of parcels (EMS, DHL, FedEx, UPS); 3. customers have the right to choose from the recent effective packaging methods of their products packaging
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Tripeptide-44 Product name Tripeptide-44 Appearance White to off-white powder Purity (HPLC) Not less than 98.0%
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High quality, competitive price, fast delivery and first-class service we possesses have won the trust and praise of customers. Standard: BP/USP/EP The purity is equal or greater than 99%. As a supplier, we can provide high-quality products. Cle
Cas:556-33-2
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inquiryHangzhou Huarong Pharm Co., Ltd.established since 2006 , has been actively developing specialty products for Finished Dosages, APIs, Intermediates, and Fine chemicals markets in North America, Europe, Korea, Japan, Mid-East and all over the World. Hu
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Cas:556-33-2
Min.Order:1 Kilogram
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inquiry1.Applied in food field.it can improve the immune system and prolong life. 2.Appliedin cosmetic field.it can improve the skin care. 3.Applied in pharmaceutical field.it can treat various dieases. 4.Our product quality assurance will make our customer
Cas:556-33-2
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inquiryAppearance:95%+ Package:R&D,Pilot run Transportation:per client require Port:Express ,Air, Sea
High quality,stable supply chain.Appearance:white/off-white or light yellow Storage:Store in cool and dry place, keep away from strong light and heat. Package:aluminum bottle,glass bottle,PTFE bottle,cardboard drum Application:This product can be use
We are a Union of chemistry in China, consists of chemists,engineers, laboratories,factories in China. We organize surplus capacity of R&D and production as well as custom synthesis for chemical products and chemical business project. We are supp
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Cas:556-33-2
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inquiryDL-phenylalanine methyl ester
1-O-(glycylglycylglycyl)-β-D-glucopyranose
A
glycine-glycine-glycine
B
glycylglycylglycyl-D,L-phenylalanine methyl ester
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% |
[2-(2-Benzyloxycarbonylamino-acetylamino)-acetylamino]-acetic acid
glycine-glycine-glycine
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. |
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% |
glycine
A
glycine-glycine-glycine
B
N-carbamoylmethyl-glycine
C
H-Gly-NH2
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% |
Conditions | Yield |
---|---|
With ammonia; water at 25℃; |
N-carboxy-glycyl=>glycyl=>glycine
glycine-glycine-glycine
Conditions | Yield |
---|---|
With borax; sodium dihydrogenphosphate at 26℃; Equilibrium constant; |
1-O-(glycylglycylglycyl)-β-D-glucopyranose mono-oxalate
A
β-D-glucose
B
glycine-glycine-glycine
Conditions | Yield |
---|---|
With β-D-glucosidase; nitrate buffer In water at 37℃; for 6h; |
1-O-(glycylglycylglycyl)-β-D-glucopyranose
A
β-D-glucose
B
glycine-glycine-glycine
Conditions | Yield |
---|---|
In water for 96h; decompn. with/without 0.1M HCl; |
glycine
A
glycine-glycine-glycine
B
tetraglycine
C
pentaglycine
D
glycylglycine
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 |
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; |
glycine
A
glycine-glycine-glycine
B
glycylglycine
D
N-(carboxymethyl)phophoroamidate
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. |
Conditions | Yield |
---|---|
at 100℃; |
glycine-glycine-glycine
Conditions | Yield |
---|---|
mit Hefe-Polypeptidase bei pH 7.0; |
glycine-glycine-glycine
Conditions | Yield |
---|---|
With palladium; acetic acid at 80℃; Hydrogenation; |
glycine-glycine-glycine
Conditions | Yield |
---|---|
With ethanol; hydrazine hydrate |
glycine-glycine-glycine
Conditions | Yield |
---|---|
With sodium hydrogencarbonate; platinum Hydrogenation.Erhitzen des Reaktionsprodukts mit H2O; |
glycine-glycine-glycine
Conditions | Yield |
---|---|
With hydrogen bromide; acetic acid |
glycine-glycine-glycine
Conditions | Yield |
---|---|
With hydrogen bromide; acetic acid |
glycine-glycine-glycine
Conditions | Yield |
---|---|
With lithium hydroxide; water; 1,2-diamino-benzene |
glycine-glycine-glycine
Conditions | Yield |
---|---|
With barium dihydroxide |
Conditions | Yield |
---|---|
dl-leucyl-diglycyl-glycine; |
N-benzyloxycarbonylglycylglycylglycylglycine
A
glycine-glycine-glycine
B
N-(Benzyloxycarbonyl)glycine
Conditions | Yield |
---|---|
Hydrolysis; |
glycine
A
Glycine anhydride
B
glycine-glycine-glycine
C
tetraglycine
D
glycylglycine
Conditions | Yield |
---|---|
With hydrogen In water at 200℃; under 187515 Torr; for 0.0333333h; Product distribution; Further Variations:; Temperatures; Reagents; |
Conditions | Yield |
---|---|
With deuteriated sodium hydroxide; dihydrogen peroxide; water-d2 at 37℃; Kinetics; |
Glycine anhydride
glycine
A
glycine-glycine-glycine
B
glycylglycine
Conditions | Yield |
---|---|
With water at 200℃; under 187515 Torr; pH=5.9; Kinetics; |
glycylglycine
glycine
A
Glycine anhydride
B
glycine-glycine-glycine
Conditions | Yield |
---|---|
In water at 200℃; under 187515 Torr; pH=5.7; Kinetics; |
((N-(tert-butoxycarbonyl)glycyl)glycyl)glycine
glycine-glycine-glycine
Conditions | Yield |
---|---|
With trifluoroacetic acid at 20℃; for 2h; |
N-(fluoren-9-ylmethoxycarbonyl)glycine
glycine-glycine-glycine
Conditions | Yield |
---|---|
Multistep reaction.; |
Conditions | Yield |
---|---|
With recombinant Pseudomonas nitroreducens IFO12694 γ-glutamyltranspeptidase at 30℃; for 0.0333333h; pH=10.5; aq. buffer; Enzymatic reaction; |
glycine-glycine-glycine
(fluorenylmethoxy)carbonyl chloride
Conditions | Yield |
---|---|
With sodium carbonate In tetrahydrofuran at 0 - 20℃; for 4h; | 100% |
Conditions | Yield |
---|---|
In toluene for 3h; Heating; | 99% |
glycine-glycine-glycine
di-tert-butyl dicarbonate
((N-(tert-butoxycarbonyl)glycyl)glycyl)glycine
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% |
Conditions | Yield |
---|---|
With palladium 10% on activated carbon; hydrogen In water under 3000.3 Torr; for 4h; | 98% |
Conditions | Yield |
---|---|
With sodium hydroxide at -13℃; for 5h; α-chymotrypsin; in ice; | 91.2% |
glycine-glycine-glycine
N-[(diethylamino)carbonothioyl]benzenecarboximidoyl chloride
Conditions | Yield |
---|---|
With potassium hydroxide In ethanol at 20℃; for 8h; | 90% |
Conditions | Yield |
---|---|
In toluene Heating; | 89% |
In toluene Reflux; Dean-Stark; | 89% |
Conditions | Yield |
---|---|
With sodium hydrogencarbonate In 1,4-dioxane; water for 24h; Ambient temperature; | 85% |
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% |
N-benzyloxycarbonyl-S-benzyl-L-cysteine succinimido-ester
glycine-glycine-glycine
Z-Cys(Bzl)-Gly3-OH
Conditions | Yield |
---|---|
With sodium hydrogencarbonate In 1,4-dioxane for 24h; Ambient temperature; | 84% |
glycine-glycine-glycine
ethanol
glycyl-glycyl-glycine ethyl ester hydrochloride
Conditions | Yield |
---|---|
With thionyl chloride for 4h; Heating; | 83% |
With hydrogenchloride for 72h; | 52.9% |
Conditions | Yield |
---|---|
In toluene for 96h; Heating; | 83% |
for 4h; Heating; | 72.2% |
glycine-glycine-glycine
succinimidyl-S-benzoylthioglycolate
benzoylmercaptoacetylglycylglycylglycine
Conditions | Yield |
---|---|
With sodium hydroxide In acetonitrile at 20 - 60℃; for 6h; | 82% |
With sodium hydroxide In water for 2.5h; Heating; |
glycine-glycine-glycine
(9H-fluoren-9-yl)methyl 1,2-dimethyl-2-((1-(3-oxo-3-(perfluorophenoxy)propyl)-1H-indol-2-yl)methyl)hydrazine-1-carboxylate
Conditions | Yield |
---|---|
With sodium hydrogencarbonate In N,N-dimethyl acetamide; water; acetonitrile at 20℃; for 22h; | 82% |
glycine-glycine-glycine
[(morpholinyl)(thiocarbonyl)]benzimidoyl chloride
Conditions | Yield |
---|---|
With potassium hydroxide In ethanol at 20℃; for 8h; | 82% |
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% |
tetrahydrofuran
glycine-glycine-glycine
[MoCl(η3-methylallyl)(CO)2(κ2(N,O)-pyridine-2-carboxaldehyde)]
[MoCl(η3-methallyl)(CO)2(NC5H4-2-C(H)=NCH2CONHCH2CONHCH2COOH)]*THF
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% |
Conditions | Yield |
---|---|
With sodium hydroxide In acetone for 0.5h; | 77% |
Conditions | Yield |
---|---|
In toluene Heating; | 77% |
In toluene for 8h; Heating; | 77% |
potassium tetrachloroplatinate(II)
glycine-glycine-glycine
cis-dichloro-bis(glycylglycylclycine)platinum(II)
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% |
methanol
glycine-glycine-glycine
methyl 2-(2-(2-aminoacetamido)acetamido)acetate hydrochloride
Conditions | Yield |
---|---|
With hydrogenchloride for 3h; Heating; | 76% |
With hydrogenchloride |
dichloro(benzene)ruthenium(II) dimer
glycine-glycine-glycine
{(η6-C6H6)Ru(NH2CH2CONCH2CONHCH2CO2H)Cl}
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% |
glycine-glycine-glycine
Conditions | Yield |
---|---|
With sodium hydrogencarbonate In water; acetonitrile | 75.4% |
glycine-glycine-glycine
4-uulfamoyl-benzoic acid 2,5-dioxo-pyrrolidin-1-yl ester
1-<((glycylglycyl)glycyl)carbonyl>-4-sulfamoylbenzene
Conditions | Yield |
---|---|
With potassium dihydrogenphosphate In acetone for 2h; Ambient temperature; | 75% |
In acetone at 20℃; for 2h; pH=7.0 - 7.5; |
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% |
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% |
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% |
glycine-glycine-glycine
Methacryloyl chloride
N-Methacryloyldiglycylglycin
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% |
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