(2S,2\'S)-2,2\'-(Hexadecanedioylbis(azanediyl))dipentanedioic+aci
Catalog Number:
(10067-270)
Supplier:
Thermo Scientific Chemicals
Description:
A broad spectrum macrolide antibiotic structurally related to erythromycin. Azithromycin dihydrate has anti-immunomodulatory/anti-inflammatory properties, which make it useful in treating cystic fibrosis
Catalog Number:
(89139-284)
Supplier:
Biotium
Description:
has recently been found to be very useful for fixing chelators or fluorescent ion indicators in situ, thus making it useful for post histological studies following the physiological experiments
Supplier:
ALADDIN SCIENTIFIC
Description:
Shipped at 4°C. Store at -20°C. Store under desiccating conditions.
Supplier:
TCI America
Description:
CAS Number: 117772-70-0
MDL Number: MFCD01862248 Molecular Formula: C38H72N2O12 Molecular Weight: 749.00 Purity/Analysis Method: >98.0% (N) Form: Crystal Specific rotation [a]20/D: -47 deg (C=2, EtOH)
Supplier:
BeanTown Chemical
Description:
CAS: 25952-53-8; EC No: 247-361-2; MDL No: MFCD00012503; RTECS: FF2200000
Crystalline/Powder; Molecular Formula: C8H17N3·HCl; MW: 191.70
Melting Point: 110-115°
Moisture Sensitive
Supplier:
TCI America
Description:
(stabilized with MEHQ)
CAS Number: 2867-47-2 MDL Number: MFCD00008589 Molecular Formula: C8H15NO2 Molecular Weight: 157.21 Purity/Analysis Method: >98.5% (GC) Form: Clear Liquid Boiling point (°C): 70 Melting point (°C): -30 Flash Point (°C): 57 Specific Gravity (20/20): 0.93
Supplier:
AMBEED, INC
Description:
1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride, Purity: 99%, CAS number: 25952-53-8, Appearance: Form: Crystal - Powder/ Colour: White - pale yellow, Storage: Keep in dark place, Sealed in dry, Store in freezer, under -20C, Size: 10G
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:
MilliporeSigma
Description:
N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride for synthesis, CAS number 25952-53-8, Chemical formula C8H17N3*HCl 25g
Supplier:
TCI America
Description:
CAS Number: 31886-58-5
MDL Number: MFCD00066273 Molecular Formula: C14H19FeN Molecular Weight: 257.16 Purity/Analysis Method: >98.0% (GC) Form: Liquid Boiling point (°C): 93 Flash Point (°C): 110 Specific Gravity (20/20): 1.22 Specific rotation [a]20/D: 15 deg (C=1, EtOH)
Supplier:
Chem Impex International
Description:
A carbodiimide coupling reagent that generates a urea by-product which can be easily removed from the reaction media by extraction with water
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.
Supplier:
Spectrum Chemicals
Description:
1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide Hydrochloride, purity: 98 %, CAS number: 25952-53-8, Molecular Formula: C8H17N3.HCl, Molecular weight: 191.71, Form: Solid, synonyms: monohydrochloride, EDAP, size: 5 g
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.
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:
AMBEED, INC
Description:
A-1210477 98%
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