O-(Carboxymethyl)hydroxylamine hemihydrochloride

98%

Reagent Code: #98294
label
Alias Carboxymethoxylamine hemihydrochloride; aminooxyacetate
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CAS Number 2921-14-4

science Other reagents with same CAS 2921-14-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 109.3 g/mol
Formula C₂H₅NO₃₁₂HCl
badge Registry Numbers
EC Number 220-862-3
MDL Number MFCD00012955
thermostat Physical Properties
Melting Point 156 °C (dec.)(lit.)
inventory_2 Storage & Handling
Storage 2~8℃

description Product Description

Used as a reagent in organic synthesis, particularly for the introduction of hydroxylamine groups into molecules. It is employed in the modification of carbohydrates and glycoproteins, aiding in the study of their structure and function. Also utilized in the preparation of oxime derivatives, which are valuable intermediates in the synthesis of pharmaceuticals and agrochemicals. Additionally, it plays a role in the development of biosensors and diagnostic tools by enabling the conjugation of biomolecules.

format_list_bulleted Product Specification

Test Parameter Specification
Purity (GC) 97.5-100%
Appearance White to off-white powder or crystals
Infrared Spectrum Conforms to Structure
Purity (Neutralization Titration) >=98.0%
Purity (Argentometric Titration) >=98.0 %
Solubility in Water Very faint turbidity

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100g
10-20 days ฿31,140.00
inventory 25g
10-20 days ฿7,880.00
inventory 5g
10-20 days ฿2,280.00
inventory 1g
10-20 days ฿600.00

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O-(Carboxymethyl)hydroxylamine hemihydrochloride
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Used as a reagent in organic synthesis, particularly for the introduction of hydroxylamine groups into molecules. It is employed in the modification of carbohydrates and glycoproteins, aiding in the study of their structure and function. Also utilized in the preparation of oxime derivatives, which are valuable intermediates in the synthesis of pharmaceuticals and agrochemicals. Additionally, it plays a role in the development of biosensors and diagnostic tools by enabling the conjugation of biomolecules.

Used as a reagent in organic synthesis, particularly for the introduction of hydroxylamine groups into molecules. It is employed in the modification of carbohydrates and glycoproteins, aiding in the study of their structure and function. Also utilized in the preparation of oxime derivatives, which are valuable intermediates in the synthesis of pharmaceuticals and agrochemicals. Additionally, it plays a role in the development of biosensors and diagnostic tools by enabling the conjugation of biomolecules.

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