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594-14-9

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594-14-9 Usage

Chemical Properties

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General Description

The multicomponent condensation of guanidine sulfate salt with H2S and CH2O was studied.

Check Digit Verification of cas no

The CAS Registry Mumber 594-14-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,9 and 4 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 594-14:
(5*5)+(4*9)+(3*4)+(2*1)+(1*4)=79
79 % 10 = 9
So 594-14-9 is a valid CAS Registry Number.
InChI:InChI=1/CH5N3.H2O4S/c2-1(3)4;1-5(2,3)4/h(H5,2,3,4);(H2,1,2,3,4)

594-14-9 Well-known Company Product Price

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  • Aldrich

  • (307394)  Guanidinesulfatesalt  99%

  • 594-14-9

  • 307394-100G

  • 793.26CNY

  • Detail
  • Aldrich

  • (307394)  Guanidinesulfatesalt  99%

  • 594-14-9

  • 307394-500G

  • 2,508.48CNY

  • Detail

594-14-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Guanidine Sulfate

1.2 Other means of identification

Product number -
Other names Guanidine, sulfate (2:1)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:594-14-9 SDS

594-14-9Relevant articles and documents

Guanidinium sulfates as directors of noncentrosymmetric structures

Brummel, Beau R.,Lee, Kinsey G.,Kolis, Joseph W.,Whitehead, Daniel C.,McMillen, Colin D.

, p. 1643 - 1656 (2021/02/26)

The structures of seven compounds based on guanidinium cations, isolated sulfate anions, and additional organic cations and solvent molecules are reported. All seven compounds, (C(NH2)3)2(SO4) (1), (C(NH2)3)3(C5H6N)(SO4)2(2), (C(NH2)3)3(C5H6N)(SO4)2·H2O (3), (C(NH2)3)3(C5H6N)(SO4)2·CH3OH (4), (C(NH2)3)11(C5H6N)(SO4)6·2.5C2H5OH (5), (C(NH2)3)3(C6H16N)(SO4)2(6), and (C(NH2)3)2(C20H26N2O2)(SO4)2(7) crystallize without a center of symmetry, and are built of related motifs of six-membered ringsviahydrogen bonding of three guanidinium cations and three sulfate anions. These six-membered rings form extended sheets and frameworks through additional hydrogen bonding interactions. The presence of additional cations and solvent molecules in varying ratios add structural diversity by modifying the guanidinium sulfate frameworks, but retaining the acentricity of the structures. The study reveals a remarkable tendency for these guanidinium sulfate frameworks to crystallize without a center of symmetry, and furthermore, in polar or chiral space groups. This provides a potential pathway for the use of hydrogen bonding interactions to design structures having interesting physical or nonlinear optical properties.

Carbonyl and oxalyl bridged bis(l,5-diaminotetrazole)-based energetic salts

Joo, Young-Hyuk,Twamley, Brendan,Shreeve, JeaN'Ne M.

experimental part, p. 9097 - 9104 (2010/04/25)

High density energetic salts containing nitrogen rich cations and carbonyl- or oxalylbis(diamino-tetrazole) anions, which were obtained from cyanogen azide and hydrazine, were readily synthesized. In every case, a new family of energetic salts 3-14 were c

Guanidinium salts, processes for their manufacture as well as microbicidal preparations containing these compounds

-

, (2008/06/13)

Guanidinium salts having the formula STR1 wherein R1 and R2 are linear alkyl residues, X is an anion, and n is 1 or 2, which possess excellent microbicidal properties, particularly against organisms which have become resistant against other active materials. Methods for preparation of the compounds and solutions containing same are disclosed.

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