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Guanidine thiocyanate solution - UltraBio™, Suitable for molecular biology, ~6 M in H2O, high purity , CAS No.593-84-0

In stock
Item Number
G755743
Grouped product items
SKU Size
Availability
Price Qty
G755743-50ml
50ml
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$121.90
G755743-250ml
250ml
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$408.90

Basic Description

Specifications & Purity UltraBio™, Suitable for molecular biology, ~6 M in H2O
Storage Temp Room temperature
Shipped In Normal
Grade for molecular biology, UltraBio™
Product Description

Guanidine thiocyanate is a chaotropic agent that functions as a strong protein denaturant. It is widely used in RNA isolation protocols. Guanidine thiocyanate can irreversibly inactivate RNase and DNase and breaks cellular membranes. It dissolves proteins by disturbing their secondary structures. Guanidine thiocyanate also separates nucleoproteins from nucleic acids and aids the digestion of the proteins with proteases. It improves the activity of proteinase K thus making it the protease of choice.

Application:

Guanidine thiocyanate solution has been used to extract:
  • plasma RNA from human immunodeficiency virus (HIV)-infected and control patients
  • total RNA from collected tissues (shoots, flowers, fruits, and seeds)
  • in reverse transcription-polymerase chain reaction (RT-PCR) analysis, RNA from teratocarcinoma cell line (Tera-1)

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organosulfur compounds
Class Thiocyanates
Subclass Not available
Intermediate Tree Nodes Not available
Direct Parent Thiocyanates
Alternative Parents Organopnictogen compounds  Organonitrogen compounds  Hydrocarbon derivatives  
Molecular Framework Not available
Substituents Thiocyanate - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Aliphatic acyclic compound
Description This compound belongs to the class of organic compounds known as thiocyanates. These are salts or esters of thiocyanic acid, with the general formula RSC#N (R=alkyl, aryl).
External Descriptors Not available

Names and Identifiers

PH 4.5-7.0 (25 °C)
IUPAC Name guanidine;thiocyanic acid
INCHI InChI=1S/CH5N3.CHNS/c2-1(3)4;2-1-3/h(H5,2,3,4);3H
InChIKey ZJYYHGLJYGJLLN-UHFFFAOYSA-N
Smiles C(#N)S.C(=N)(N)N
Isomeric SMILES C(#N)S.C(=N)(N)N
WGK Germany 2
RTECS XL1225000
UN Number 1759
Packing Group III
Molecular Weight 118.16
Beilstein 3563461
Reaxy-Rn 3563461
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3563461&ln=

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Chemical and Physical Properties

Melt Point(°C) 118-122°C
Molecular Weight 118.160 g/mol
XLogP3
Hydrogen Bond Donor Count 4
Hydrogen Bond Acceptor Count 3
Rotatable Bond Count 0
Exact Mass 118.031 Da
Monoisotopic Mass 118.031 Da
Topological Polar Surface Area 101.000 Ų
Heavy Atom Count 7
Formal Charge 0
Complexity 57.600
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 2

Citations of This Product

1. Jie Lian, Wenyu Gong, Jianing Guo, Mingxing Wu.  (2024)  Design highly effective B or N doped mesoporous carbon fibers catalysts for I3-/I- redox couple regeneration in carbon-based dye-sensitized solar cells.  Arabian Journal of Chemistry,  17  (105817). 
2. Chunmei Lv, Jing Liu, Borong Lu, Ke Ye, Guiling Wang, Kai Zhu, Dianxue Cao, Ying Xie.  (2024)  Iron-doping and facet engineering of NiSe octahedron for synergistically enhanced triiodide reduction activity in photovoltaics.  JOURNAL OF COLLOID AND INTERFACE SCIENCE,  663  (674). 
3. Baorui Liu, Hongqing Cheng, Fangchao Cheng, Dongying Hu.  (2025)  Lignosulfonate-Induced orientation of Poly(3,4-ethlylenedioxythiophene) for enhanced efficiency in bifacial Dye-Sensitized solar cells.  CHEMICAL ENGINEERING JOURNAL,  505  (159499). 
4. Yanjun Xing, Zhiqiang Deng, Qiuxiang Wang, Jiaxing Xiong, Xiaohui Liu, Like Huang, Yuejin Zhu, Jing Zhang.  (2024)  Polymer Lewis Base for Improving the Charge Transfer in Tin–Lead Mixed Perovskite Solar Cells.  Nanomaterials,  14  (5): (437). 
5. Wei Ding, Chen Bai, Yuxuan Ren, Dong Fang, Jing Bai, Jiali Wen, Baoxiu Mi, Dapeng Cao, Zhiqiang Gao.  (2024)  Synergetic effects of recombination-blocking, band-bending and gap-state manipulation by interfacial engineering in solid-state DSSCs comprising Cs2SnI6 electrolyte.  Surfaces and Interfaces,  48  (104246). 

Solution Calculators

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