Boc-Gln(Trt)-OH
Supplier:
THERMO FISHER SCIENTIFIC CHEMICALS
Description:
Ethyl acetate for pesticide residue analysis
Supplier:
THERMO FISHER SCIENTIFIC CHEMICALS
Description:
Ethyl acetate 99.5% ACS for spectroscopy
Supplier:
Adipogen
Description:
Antibiotic
Catalog Number:
(700002-760)
Supplier:
Spectrum Chemicals
Description:
1-Hexanol, Purified is an organic alcohol that is a colorless liquid that is slightly soluble in water and most often used in the perfume industry. It is miscible with ethanol and ether. The Purified Grade describes chemicals of good quality where there are no official standards.
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Catalog Number:
(TCE0478-025G)
Supplier:
TCI America
Description:
[Protecting Reagent for Aldehydes and Ketones]
CAS Number: 7381-30-8 MDL Number: MFCD00009640 Molecular Formula: C8H22O2Si2 Molecular Weight: 206.43 Purity/Analysis Method: >97.0% (GC) Form: Clear Liquid Boiling point (°C): 166 Flash Point (°C): 46 Specific Gravity (20/20): 0.84
Supplier:
MP Biomedicals
Description:
(6R)-5,6,7,8-Tetrahydro-L-biopterin Dihydrochloride is necessary in vivo for the conversion of phenylalanine to tyrosine and for the production of the hormone epinephrine and of the monoamine neurotransmitters, serotonin, dopamine, and norepinephrine. It is also involved in apoptosis and other cellular events mediated by nitric oxide production and catalyzes the cleavage of alkylglycerol ethers.
Catalog Number:
(101815-572)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 023218-500MG , MDL Number: MFCD08061061
Catalog Number:
(G-1775.0001BA)
Supplier:
Bachem Americas
Description:
Also known as dioxopiperazines, piperazine-2,5-diones or DKPs. Diketopiperazines may occur as by-products during peptide synthesis or during the degradation of peptides. These cyclic dipeptides have been detected as taste-modulating compounds in food, they often show biological activity. DKPs are valuable chiral synthons, employed e.g. in Schöllkopf's versatile bislactim ether approach. They also have found use as catalysts for enantioselective synthesis, e.g. in the asymmetric Strecker reaction. See also the TRH metabolite cyclo(-His-Pro), G-1745, and cyclo(-Asp-Phe), G-1695, the major degradation product of aspartame.
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 049599-2.5G , MDL Number: MFCD13560001
Supplier:
Bachem Americas
Description:
Also known as dioxopiperazines, piperazine-2,5-diones or DKPs. Diketopiperazines may occur as by-products during peptide synthesis or during the degradation of peptides. These cyclic dipeptides have been detected as taste-modulating compounds in food, they often show biological activity. DKPs are valuable chiral synthons, employed e.g. in Schöllkopf's versatile bislactim ether approach. They also have found use as catalysts for enantioselective synthesis, e.g. in the asymmetric Strecker reaction. See also the TRH metabolite cyclo(-His-Pro), G-1745, and cyclo(-Asp-Phe), G-1695, the major degradation product of aspartame.
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 050000-500MG , MDL Number: MFCD13560402
Catalog Number:
(G-1710.0250BA)
Supplier:
Bachem Americas
Description:
Also known as dioxopiperazines, piperazine-2,5-diones or DKPs. Diketopiperazines may occur as by-products during peptide synthesis or during the degradation of peptides. These cyclic dipeptides have been detected as taste-modulating compounds in food, they often show biological activity. DKPs are valuable chiral synthons, employed e.g. in Schöllkopf's versatile bislactim ether approach. They also have found use as catalysts for enantioselective synthesis, e.g. in the asymmetric Strecker reaction. See also the TRH metabolite cyclo(-His-Pro), G-1745, and cyclo(-Asp-Phe), G-1695, the major degradation product of aspartame.
Catalog Number:
(16194-909)
Supplier:
Qorpak
Description:
Reduce breakage and lab mishaps with these safety coated clear medium round bottles.
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Supplier:
MP Biomedicals
Description:
DL-Dithiothreitol is also known as Clelands reagent; Protective agent for sulfhydryl groups (-SH). Quantitatively reduces disulfides (-S-S- to -SH). In this reaction the DTT is oxidized to the cyclic disulfide which ensures the reduction of other disulfides in solution. Disulfide reduction occurs quickly at pH 8.
DTT has been used:
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