You Searched For: 5,6-Diamino-1,3-diethyluracil+hydrochloride


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Supplier: Thermo Scientific Chemicals
Description: L-Aspartic acid di-tert-butyl ester hydrochloride, 98%
Supplier: Thermo Scientific
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: (TCM0868-025G)
Supplier: TCI America
Description: CAS Number: 60-56-0
MDL Number: MFCD00179321
Molecular Formula: C4H6N2S
Molecular Weight: 114.17
Purity/Analysis Method: >98.0% (HPLC,T)
Form: Crystal
Melting point (°C): 145
Flash Point (°C): 110

Catalog Number: (CAJT2077-6)
Supplier: AVANTOR PERFORMANCE MATERIAL LLC
Description: L(+)-Glutamic acid 98.5-101.5% USP, Multi-Compendial, J.T.Baker®

Supplier: Bachem Americas
Description: Sequence: H-Glu-OH

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: (TCH0752-025G)
Supplier: TCI America
Description: CAS Number: 1476-98-8
MDL Number: MFCD00135598
Molecular Formula: C20H26N2O2
Molecular Weight: 362.90
Purity/Analysis Method: >98.0% (T,HPLC)
Form: Crystal
Specific rotation [a]20/D: 188 deg (C=1.3, H2O)

Supplier: Enzo Life Sciences
Description: Highly potent and selective serotonin uptake inhibitor

Catalog Number: (RK30212)
Supplier: Restek
Description: Mix contains: Bromodichloromethane (75-27-4); Bromoform (75-25-2); Carbon tetrachloride (56-23-5); Chlorobenzene (108-90-7); 2-Chloroethyl vinyl ether (110-75-8); Chloroform (67-66-3); Dibromochloromethane (124-48-1); 1,2-Dichlorobenzene (95-50-1); 1,3-Dichlorobenzene (541-73-1); 1,4-Dichlorobenzene (106-46-7); 1,1-Dichloroethane (75-34-3); 1,2-Dichloroethane (107-06-2); 1,1-Dichloroethene (75-35-4); trans-1,2-Dichloroethene (156-60-5); 1,2-Dichloropropane (78-87-5); cis-1,3-Dichloropropene (10061-01-5); trans-1,3-Dichloropropene (10061-02-6); Methylene chloride (dichloromethane) (75-09-2); 1,1,2,2-Tetrachloroethane (79-34-5); Tetrachloroethene (127-18-4); 1,1,1-Trichloroethane (71-55-6); 1,1,2-Trichloroethane (79-00-5); Trichloroethene (79-01-6).


Catalog Number: (75810-534)
Supplier: Spectrum Chemical Mfg. Corp.
Description: L-Asparagine, Monohydrate, FCC - The FCC grade meets the requirements of the Food Chemical Codex indicates and is suitable for all food, beverage and nutritional supplement applications. Spectrum Chemical offers over 300 Food grade chemical ingredients packaged in laboratory size bottles to production drum quantities and are manufactured, packaged and stored under current Good Manufacturing Practices (cGMP) per 21CFR part 211 in FDA registered and inspected facilities.

Catalog Number: (CAAAJ63830-MF)
Supplier: Thermo Scientific Chemicals
Description: An NMDA receptor antagonist; stimulates dopamine release

Catalog Number: (89151-456)
Supplier: Enzo Life Sciences
Description: Vitamin D3 precursor


Supplier: TCI America
Description: CAS Number: 628-13-7
MDL Number: MFCD00012802
Molecular Formula: C5H5N
Molecular Weight: 115.56
Purity/Analysis Method: >98.0% (HPLC,T)
Form: Crystal
Color: White
Boiling point (°C): 224
Melting point (°C): 147
Supplier: Thermo Scientific Chemicals
Description: L(+)-Ornithine hydrochloride 99%
Catalog Number: (CAAAJ62011-MB)
Supplier: Thermo Scientific Chemicals
Description: Calmodulin antagonist

Supplier: Thermo Scientific
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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