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Semicarbazide hydrochloride, 99%, Thermo Scientific Chemicals

Urease substrate and MAO inhibitor

$53.14 - $558.81

Chemical Identifiers

CAS 563-41-7
Molecular Formula CH6ClN3O
Molecular Weight (g/mol) 111.53
MDL Number MFCD00013009
InChI Key XHQYBDSXTDXSHY-UHFFFAOYSA-N
Synonym semicarbazide hydrochloride, aminourea hydrochloride, semicarbazide hcl, hydrazinecarboxamide hydrochloride, hydrazinecarboxamide, monohydrochloride, semicarbazide chloride, amidourea hydrochloride, carbamylhydrazine hydrochloride, semicarbazide monohydrochloride, semicarbazide, monohydrochloride
PubChem CID 11236
ChEBI CHEBI:82532
IUPAC Name aminourea;hydrochloride
SMILES [H+].[Cl-].NNC(N)=O
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Products 3
Catalog Number Mfr. No. Quantity Price Quantity  
Catalog Number Mfr. No. Quantity Price Quantity  
AAA1166822
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Thermo Scientific Chemicals
A1166822
100 g N/A
 
AAA1166836
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Thermo Scientific Chemicals
A1166836
500 g N/A
 
AAA116680E
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Thermo Scientific Chemicals
A116680E
2500 g N/A
 
Description

Description

Semicarbazide hydrochloride is used as urease substrate and MAO inhibitor. Derivatizing agent for carbonyl compounds as their semicarbazones which produces crystalline compounds with characteristic melting points. Also used in heterocyclic synthesis. Semicarbazone formation has been used to separate carbonyl compounds from mixtures by adsorption onto silica gel from a hydrocarbon solution. Regeneration is by hydrolysis with oxalic acid.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Semicarbazide hydrochloride is used as urease substrate and MAO inhibitor. Derivatizing agent for carbonyl compounds as their semicarbazones which produces crystalline compounds with characteristic melting points. Also used in heterocyclic synthesis. Semicarbazone formation has been used to separate carbonyl compounds from mixtures by adsorption onto silica gel from a hydrocarbon solution. Regeneration is by hydrolysis with oxalic acid.

Solubility
Soluble in water (>100g/L).

Notes
Store in cool, dry conditions in well sealed container. Store away from oxidizing agent.
Specifications

Chemical Identifiers

563-41-7
111.53
XHQYBDSXTDXSHY-UHFFFAOYSA-N
11236
aminourea;hydrochloride
CH6ClN3O
MFCD00013009
semicarbazide hydrochloride, aminourea hydrochloride, semicarbazide hcl, hydrazinecarboxamide hydrochloride, hydrazinecarboxamide, monohydrochloride, semicarbazide chloride, amidourea hydrochloride, carbamylhydrazine hydrochloride, semicarbazide monohydrochloride, semicarbazide, monohydrochloride
CHEBI:82532
[H+].[Cl-].NNC(N)=O

Specifications

563-41-7
White
Odorless
H2NCONHNH·HCl
100 g
3593642
semicarbazide hydrochloride, aminourea hydrochloride, semicarbazide hcl, hydrazinecarboxamide hydrochloride, hydrazinecarboxamide, monohydrochloride, semicarbazide chloride, amidourea hydrochloride, carbamylhydrazine hydrochloride, semicarbazide monohydrochloride, semicarbazide, monohydrochloride
XHQYBDSXTDXSHY-UHFFFAOYSA-N
aminourea;hydrochloride
11236
111.53
Crystalline
∼176°C (decomposition)
1.5
CH6ClN3O
MFCD00013009
UN2811
14,8444
Soluble in water (>100g/L).
[H+].[Cl-].NNC(N)=O
111.53
CHEBI:82532
99%
Semicarbazide hydrochloride
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Safety and Handling

Safety and Handling

GHS H Statement
H301-H315-H319-H335
Toxic if swallowed.
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.

P201-P202-P264b-P270-P280-P280i-P301+P310-P302+P352-P305+P351+P338-P308+P313-P310-P330-P332+P313-P362-P501c

H301-H315-H319-H351

DOTInformation : Transport Hazard Class: 6.1; Packing Group: III; Proper Shipping Name: TOXIC SOLIDS, ORGANIC, N.O.S.

EINECSNumber : 209-247-0

RTECSNumber : VT3500000

TSCA : Yes

Recommended Storage : Ambient temperatures

SDS
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RUO – Research Use Only