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Guanidine thiocyanate

HCID 65046
NotesReactions
Basic informationOverviewNames & identifiersPropertiesSafety & regulationChemistry & industryRelated reactionsCompound notes
Substructure searchFind similar structures

Basic information

CAS
593-84-0
Standard SMILES
N#CS.N=C(N)N
InChIKey
ZJYYHGLJYGJLLN-UHFFFAOYSA-N
Molecular formula
CH5N3.CHNS
Average molar mass
118.16 g/mol
Monoisotopic mass
118.03131738

Overview

a powerful chaotropic agent

Names & identifiers

Preferred name
Guanidine thiocyanate
IUPAC
guanidine;thiocyanic acid
English name
Guanidine thiocyanate
Molecular formula
CH5N3.CHNS
Molecular weight
118.16

Names & synonyms

Guanidine thiocyanate593-84-0Guanidinium thiocyanateGuanidine, monothiocyanateBUFFER AVLGCA2EU297UGuSCNNSC-2119DTXSID6060478RefChem:144652DTXCID1042601209-812-1
Show more names
GUANIDINIUM ISOTHIOCYANATEGdmSCNabs9138usafek-705GUANIDIN THIOCYGTC,guanidineth
guanidine isothiocyanateguanidine;thiocyanic acidGuanidinium rhodanideMFCD00013027USAF EK-705M01833GTCguanidinethiocyanate

Database identifiers

CAS
593-84-0
PubChem CID
65046
DTXSID
DTXSID6060478
UNII
GCA2EU297U
EC Number
209-812-1

Properties

Computed structural properties

Topological polar surface area
101 Ų
Hydrogen bond donors
4
Hydrogen bond acceptors
3
Rotatable bonds
0
Heavy atoms
7
Formal charge
0
Complexity
57.6

Experimental & physicochemical properties

Chemical ClassesOther Uses -> Biochemical Research
Physical Description · 2 items

Liquid; Dry Powder

White crystalline solid; Hygroscopic; [Sigma-Aldrich MSDS]

Physicochemical properties

Melting point
120 · 120-122 °C(lit.)
Density
1.103 g/mL · 1.103 g/mL at 20 °C
bulk density
630 kg/m3 · 630kg/m3
vapor pressure
0 Pa · 0Pa at 20℃
refractive index
20 · n20/D 1.482
storage temp.
20 · 20-25°C
solubility
2 O: · H2O: 6 M at 20 °C, clear, colorless
form
Crystals or Crystalline Powder
pka
12.5 · 12.5[at 20 ℃]
color
White or colorless
Specific Gravity
1.152 · 1.152

Safety & regulation

Safety information is for reference only and does not replace the supplier’s Safety Data Sheet (SDS), applicable regulations, or professional assessment.

GHS classification

GHS Classification · 5 items

This chemical does not meet GHS hazard criteria for 0.2% (1 of 404) of reports.

Danger

H302+H312+H332 (45.3%): Harmful if swallowed, in contact with skin or if inhaled [Warning Acute toxicity, oral; acute toxicity, dermal; acute toxicity, inhalation]

P260, P261, P264, P264+P265, P270, P271, P273, P280, P301+P317, P301+P330+P331, P302+P352, P302+P361+P354, P304+P340, P305+P354+P338, P316, P317, P321, P330, P362+P364, P363, P405, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 404 reports by companies from 22 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Hazard information

Regulatory Information · 4 items

Chemical: Thiocyanic acid, compound with guanidine (1:1)

Thiocyanic acid, compd. with guanidine (1:1) is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of Thiocyanic acid, compd. with guanidine (1:1) are required to report information about their production and use of this chemical to the EPA under the Toxic Substances Control Act (TSCA). (40 eCFR Part 711)

REACH registered substance: Guanidinium thiocyanate (EC: 209-812-1)

Guanidinium thiocyanate: Does not have an individual approval but may be used under an appropriate group standard

Hazards SummaryIntraperitoneal LD50 (mouse) = 300 mg/kg; [RTECS] Causes burns; Inhalation may cause corrosive injuries to upper respiratory tract and lungs; Harmful by ingestion; [Sigma-Aldrich MSDS] See Guanidine. See Sodium thiocyanate.
Hazard Classes and CategoriesAcute Tox. 4 (98.3%)

Safety & protection

Chemistry & industry

Pharmacology

MeSH Pharmacological Classification · 1 item

Substances used on inanimate objects that destroy harmful microorganisms or inhibit their activity. Disinfectants are classed as complete, destroying SPORES as well as vegetative forms of microorganisms, or incomplete, destroying only vegetative forms of the organisms. They are distinguished from ANTISEPTICS, which are local anti-infective agents used on humans and other animals. (From Hawley's Condensed Chemical Dictionary, 11th ed)

Uses & manufacturing

UsesA powerful chaotropic agent. [ChemIDplus] Used for RNA isolation and can solubilize proteins; [Santa Cruz Biotechnology]
U.S. Production2023: <50,000 lb
Consumer UsesLaboratory chemicals
Industry UsesLaboratory chemicals
General Manufacturing Information · 2 items

Other (requires additional information)

Thiocyanic acid, compd. with guanidine (1:1): ACTIVE

Applications · 6 items

DescriptionGuanidine thiocyanate is one of the cheapest and easiest to prepare of the guanidine salts. Guanidine Thiocyanate is an ultrapure, molecular biology grade reagent. It is free of detectable nuclease and protease activity and is a strong protein denaturant, as both the guanidinium cation and the thiocyanate anion are chaotropic agents. It is provided in one bottle containing 500 g. It is recommended for isolation of RNA, especially for tissues such as pancreas with high levels of RNase activity. In solution, it is known as guanidinium thiocyanate. Guanidine Thiocyanate is thoroughly tested for contaminating nonspecific endonuclease, exonuclease, and RNase activity.

Related reactions

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Compound notes

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On this pageBasic informationOverviewNames & identifiersPropertiesSafety & regulationChemistry & industryRelated reactionsCompound notes
Odor
Odorless
PH Range
4.8 · 4.8 - 6.0
PH
4.8 · 4.8-6.0 (1420g/l, H2O, 20℃)(saturated solution)
biological source
synthetic (organic)
Water Solubility
Soluble in water and ethanol
Sensitive
Light Sensitive
BRN
3563461 · 3563461
Stability
Stability Stable, but light sensitive. Incompatible with acids (contact releases very toxic gas), strong oxidising agents.
InChI
1S/CH5N3.CHNS/c2-1(3)4;2-1-3/h(H5,2,3,4);3H
InChIKey
ZJYYHGLJYGJLLN-UHFFFAOYSA-N
SMILES
SC#N.NC(N)=N
LogP
-1.5 · -1.5--1.42 at 20℃
CAS DataBase Reference
593 · 593-84-0(CAS DataBase Reference)
FDA UNII
2 EU297U · GCA2EU297U
EPA Substance Registry System
Thiocyanic acid, compd. with guanidine (1:1) (593-84-0)
Absorption
280 nm · cut-off at 280nm in H2O at 6M
UNSPSC Code
51102829 · 51102829
NACRES
21 · NB.21
Symbol(GHS)
5 · GHS05,GHS07
Signal word
Danger
Hazard statements
302 · H302+H312+H332-H314-H412
Precautionary statements
260 · P260-P273-P280-P303+P361+P353-P304+P340+P310-P305+P351+P338
PPE
95 · dust mask type N95 (US), Eyeshields, Gloves
Hazard Codes
Xn,T,C
Risk Statements
20 · 20/21/22-32-52/53-36/37/38-34
Safety Statements
36 · 36/37-61-13-36-26-45-36/37/39
RIDADR
1759 · 1759
WGK Germany
2 · 2
RTECS
1225000 · XL1225000
F
3 · 3-10
TSCA
TSCA listed
HazardClass
8 · 8
PackingGroup
III
HS Code
29252000 · 29252000
Storage Class
8 B · 8B - Non-combustible corrosive hazardous materials
Hazard Classifications
4 DermalAcute · Acute Tox. 4 DermalAcute Tox. 4 InhalationAcute Tox. 4 OralAquatic Chronic 3Eye Dam. 1Skin Corr. 1C
REACH Registrations
Active
Limited Quantities
5 kg · 5.0 kg (11 lbs) (solid)
Excepted Quantities
Max Inner Pack (30g or 30ml) and Max Outer Pack (1Kg or 1L)
Protective Action Criteria (PAC) · 3 items

1.1 [mg/m3]

12 [mg/m3]

70 [mg/m3]

Toxicology

Adverse EffectsDermatotoxin - Skin burns.

Safety data

F
3-10
PPE
dust mask type N95 (US), Eyeshields, Gloves
wgk
2
tsca
TSCA listed
rtecs
XL1225000
ridadr
1759
hs_code
29252000
risk_code
20/21/22-32-52/53-36/37/38-34
Signal word
Danger
Symbol(GHS)
GHS05,GHS07
hazard_code
Xn,T,C
safety_code
36/37-61-13-36-26-45-36/37/39
hazard_class
8
Storage Class
8B - Non-combustible corrosive hazardous materials
packing_group
III
Hazard statements
H302+H312+H332-H314-H412
Limited Quantities
5.0 kg (11 lbs) (solid)
Excepted Quantities
Max Inner Pack (30g or 30ml) and Max Outer Pack (1Kg or 1L)
REACH Registrations
Active
Hazard Classifications
Acute Tox. 4 DermalAcute Tox. 4 InhalationAcute Tox. 4 OralAquatic Chronic 3Eye Dam. 1Skin Corr. 1C
Precautionary statements
P260-P273-P280-P303+P361+P353-P304+P340+P310-P305+P351+P338

UsesGuanidine thiocyanate is a potent protein denaturant (stronger than guanidine HCl) often used in the isolation of intact ribonucleic acid to eliminate RNase activity. RNase can recover activity after boiling, but is irreversibly inactivated in a 4 M solution of guanidine thiocyanate. Such solutions, to which the reducing agent b-mercaptoethanol is often added, are used to inactivate RNAse when isolating RNA from tissues that are rich in RNase, such as liver. Total nuclear and cytoplasmic RNA may be isolated this way. A protocol for extracting RNA with guanidine isothiocyanate has been published.In the presence of guanidine thiocyanate, proteins dissolve readily, cellular structures disintegrate and nucleoproteins dissociate from nucleic acids, as protein secondary structure is lost.

UsesPotent protein denaturant used in isolation of intact DNA, RNA.

UsesGuanidine thiocyanate is a useful tool for RNA isolation and protein solubilization. It is involved in the quantification of mRNA from hepatocytes. It acts as a medium for blood smaple lystae in order to maintain the integrity of nucleic acid. It is a chaotropic agent, mainly involved in the extraction of DNA and RNA. It is utilized to deactivate the influenza virus.

UsesGuanidine thiocyanate has been used as a component of the stabilization buffer for RNA lysis. It can be used for deactivation of endogenous RNases leading to denaturation of nucleoprotein complexes. It is also suitable for denaturation of macromolecules such as nucleic acids and proteins and for RNA isolation.

General DescriptionGuanidine thiocyanate is chaotropic salts which lyse cells and along with nuclease binding matrix it is also seen to inhibit nuclease activity during extraction of DNA. It works as a strong RNase inhibitor in extraction buffers.

Preparation methods · 1 item

Preparationmethod for preparing guanidine thiocyanate, comprising the following process flow: (1) Guanidine carbonate and ammonium sulfate in a weight ratio of 2:1 are placed in a reaction vessel and reacted at 45-95℃ for 1.5 hours to obtain crude guanidine thiocyanate. (2) Dissolution: At room temperature, the crude guanidine thiocyanate is dissolved in water at a ratio of 0.5:1. (3) Filtration: Impurities such as raw materials and reaction by-products are removed by filtration. (4) Dehydration: The mother liquor after filtration is dehydrated at high temperature. (5) Crystallization: The solution is cooled, concentrated, and crystallized to obtain high-purity guanidine thiocyanate.

Suppliers100 total

国药集团化学试剂有限公司86-21-63210123 · [email protected]
北京华美互利生物化工010-56205725 · [email protected]
梯希爱(上海)化成工业发展有限公司021-67121386 · [email protected]
衢州润东化工有限公司0570-8789886 18892685668 · [email protected]
上海阿拉丁生化科技股份有限公司400-6206333 13167063860 · [email protected]
INTATRADE GmbH+49 3493/605464 · [email protected]
上海如吉生物科技发展有限公司+86-21-65211385-8001 36031160 · [email protected]
南京兰亚化工贸易有限公司+86-25-8331-5620 · [email protected]
上海将来实业股份有限公司400-0066400 13621662912 · [email protected]
武汉易泰科技有限公司上海分公司18930552037 · [email protected]
大连美仑生物技术有限公司0411-62910999 13889544652 · [email protected]
阿法埃莎(中国)化学有限公司400-6106006 · [email protected]
安耐吉化学&3A(安徽泽升科技股份有限公司)400-0056266 · [email protected]
秦皇岛天资化工有限公司13313337629 15227250682 · [email protected]
上海瀚鸿科技股份有限公司021-54306202 13764082696 · [email protected]
上海融禾医药科技发展有限公司17301719108 13341702378 · [email protected]
嘉兴市艾森化工有限公司0573-85285100 18627885956 · [email protected]
上海泰坦科技股份有限公司4006009262 13023226327 · [email protected]
南京美博生物科技有限公司025-58619198 · [email protected]
山东西亚化学有限公司13355009207 13355009207 · [email protected]
玛雅试剂+86 (573) 82222445 (0)18006601000 452520369 · [email protected]
四川库利南科技有限公司400-1166-196 18981987031 · [email protected]
天津希恩思生化科技有限公司400 638 7771 · [email protected]
河南萬象化工有限公司(优势生产供应!)0371-56669001 · [email protected]
湖南汇百侍生物科技有限公司0731-85526065 13308475853 · [email protected]
斯百全化学(上海)有限公司021-021-021-67601398-809-809-809 15221380277 · [email protected]
上海源叶生物科技有限公司18916372613 · [email protected]
南京爱莉生物科技有限公司025-83208295 18913388297 · [email protected]
上海思域化工科技有限公司86-21-34053660 · [email protected]
赛默飞世尔科技(中国)有限公司800-810-5118 · [email protected]
北京伊诺凯科技有限公司400-810-7969 010-59572699 · [email protected]
Wuhan NCE Biomedical Co.,Ltd.4000-027-021 |24 +86-13986109188 | +86-15623472865 | +81-08033611988
江苏艾康生物医药研发有限公司025-66113011 13913916777 · [email protected]
TCI AMERICA800-4238616 · [email protected]
TOKYO CHEMICAL INDUSTRY CO., LTD.03-36680489 · [email protected]
TCI Europe320-37350700 · [email protected]
南京杜莱生物技术有限公司025-84699383-8003;025-846993838003-8003 18013301590 · [email protected]
南京生利德生物科技有限公司025-57798810 18652991625 · [email protected]
重庆卡兰医药有限公司023-62879767 · [email protected]
北京环宇世纪化学科技有限公司hysj_bj.com
上海湄水化工科技有限公司021-60549325 18616193163
上海将来实业股份有限公司400-0066400 13621662912 · [email protected]
上海将来实业股份有限公司021-61552785 · [email protected]
HBCChem, Inc.+1-510-219-6317 · [email protected]
郑州鸿晟医药科技有限公司0371-0371-13526885213 15637198702 · [email protected]
安倍医疗器械贸易(上海)有限公司400-1500-680 021-62402299 · [email protected]
成都零六生物科技有限公司400-1166-196 13458535857 · [email protected]
上海创赛科技有限公司400-6087598 15021221957 · [email protected]
潍坊鲁泽新材料有限公司0536-7971999 17176128999 · [email protected]
上海御略医药科技有限公司021-60345187 13671753212 · [email protected]