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Safety Information

01-5220

Sigma-Aldrich

Ammonium thiocyanate solution

0.1 M, 1/10 N

Synonym(s):

Ammonium rhodanide solution

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About This Item

Linear Formula:
NH4SCN
CAS Number:
Molecular Weight:
76.12
Beilstein:
3595135
MDL number:
UNSPSC Code:
12352106
PubChem Substance ID:

form

liquid

availability

available only in Japan

concentration

0.1 M
1/10 N

SMILES string

N.SC#N

InChI

1S/CHNS.H3N/c2-1-3;/h3H;1H3

InChI key

SOIFLUNRINLCBN-UHFFFAOYSA-N

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Storage Class Code

12 - Non Combustible Liquids

WGK

nwg

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

01-5220-5-500ML-J:


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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The velocity fields within the impeller passages of three different impellers of the Kyoto-NTN bio-centrifugal ventricular assist device are measured using laser Doppler velocimetry in this study. The 16 forward-swept-blade impeller has better performance than the 16 straight-blade and 8
Mark A Zottola
Journal of molecular graphics & modelling, 28(2), 183-186 (2009-07-25)
Cyanide (CN) is considered to be a terrorist chemical weapon due to its ready availability in multi-kilogram quantities and multi-modal means of intoxication. The body uses the sulfur transferase enzyme rhodanese to detoxify cyanide via conversion of cyanide to thiocyanate.
Javad Azizian et al.
Molecular diversity, 6(3-4), 223-226 (2004-04-08)
A new one-pot four component procedure for synthesis of densely functionalized pyrroles using commercially available ninhydrin with phosphorane intermediates produced in the reaction between triphenylphosphine, ammonium thiocyanate (or ammonium acetate) and various dialkyl acetylenedicarboxylates was developed.

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