Pyrazine-2,6-diamine+hydrochloride
Catalog Number:
(IC10360010)
Supplier:
MP Biomedicals
Description:
Soluble in water(1 mg/mL, Clear orange to brown solution).
Supplier:
TCI America
Description:
[Coupling Agent for Peptides Synthesis]
CAS Number: 25952-53-8 MDL Number: MFCD00012503 Molecular Formula: C8H17N3 Molecular Weight: 191.70 Purity/Analysis Method: >98.0% (T) Form: Crystal Melting point (°C): 115 Storage Temperature: 0-10°C
Supplier:
Invitrogen
Description:
Thermo Scientific Pierce Premium Grade EDC is our highest quality formulation of this popular carbodiimide crosslinker, specially characterized for applications where product integrity and risk minimization are paramount.
Catalog Number:
(BT134580-1G)
Supplier:
BeanTown Chemical
Description:
CAS: 106092-09-5; MDL No: MFCD07368003
Solid; Molecular Formula: C7H11N3S; MW: 169.25
Melting Point: 230-231°
Light Sensitive, Moisture Sensitive
Supplier:
AMBEED, INC
Description:
(2,4-Diaminopteridin-6-yl)methanol hydrochloride 97%
Supplier:
Invitrogen
Description:
Thermo Scientific Pierce EDC is a carboxyl- and amine-reactive zero-length crosslinker. EDC reacts with a carboxyl group first and forms an amine-reactive O-acylisourea intermediate that quickly reacts with an amino group to form an amide bond with release of an isourea by-product. The intermediate is unstable in aqueous solutions and so two-step conjugation procedures rely on N-hydroxysuccinimide (NHS) for stabilization. Failure to react with an amine will result in hydrolysis of the intermediate, regeneration of the carboxyl, and release of an N-substituted urea. A side reaction is the formation of an N-acylurea, which is usually restricted to carboxyls located in hydrophobic regions of proteins.
Supplier:
G-Biosciences
Description:
EDC is a heterobifunctional, water-soluble, zero-length carbodiimide crosslinker that is used to couple carboxyl groups to primary amines. EDC activates carboxyl groups first and forms amine reactive O-acylisourea imtermediate that spontaneously reacts with primary amines to form an amide bond and isourea by-product.
Catalog Number:
(AAJ60350-03)
Supplier:
Thermo Scientific Chemicals
Description:
Competitive reversible H-1 receptor antagonist
Supplier:
AMBEED, INC
Description:
Neutral red 98% BS
Supplier:
BeanTown Chemical
Description:
CAS: 317-34-0; EC No: 206-264-5; MDL No: MFCD00013221; RTECS: XH5600000
UN No: UN2811; Haz Class: 6.1; Packing Group: III
Powder; Molecular Formula: C7H8N4O2·0.5C2H8N2; MW: 210.21
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 059226-10G , MDL Number: MFCD00023187
Supplier:
AAT BIOQUEST INC
Description:
N-FMOC-ethylenediamine is a monoprotected diamine that is widely used as a building block in bioconjugate chemistry.
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Catalog Number:
(TCA2721-5G)
Supplier:
TCI America
Description:
CAS Number: 935521-01-0
MDL Number: MFCD08063180 Molecular Formula: C13H17N3 Molecular Weight: 251.76 Purity/Analysis Method: >98.0% (HPLC,T) Form: Crystal Melting point (°C): 264
Catalog Number:
(103011-346)
Supplier:
Anaspec Inc
Description:
Bind to DNA/RNA (red fluorescence) upon oxidation. Store at -20C desiccated and protected from light
Catalog Number:
(103523-940)
Supplier:
Invitrogen
Description:
Thermo Scientific Pierce EDC is a carboxyl- and amine-reactive zero-length crosslinker. EDC reacts with a carboxyl group first and forms an amine-reactive O-acylisourea intermediate that quickly reacts with an amino group to form an amide bond with release of an isourea by-product. The intermediate is unstable in aqueous solutions and so two-step conjugation procedures rely on N-hydroxysuccinimide (NHS) for stabilization. Failure to react with an amine will result in hydrolysis of the intermediate, regeneration of the carboxyl, and release of an N-substituted urea. A side reaction is the formation of an N-acylurea, which is usually restricted to carboxyls located in hydrophobic regions of proteins.
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