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Home > Products >  AMINOMETHANAMIDINE HYDROCHLORIDE

AMINOMETHANAMIDINE HYDROCHLORIDE CAS NO.50-01-1

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  • Min.Order: 1 Kilogram
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  • Available Specifications:

    98%(1-5)Kilogram

  • Product Details

Keywords

  • 50-01-1
  • CH6ClN3
  • Guanidine hydrochloride

Quick Details

  • ProName: AMINOMETHANAMIDINE HYDROCHLORIDE
  • CasNo: 50-01-1
  • Molecular Formula: CH6ClN3
  • Appearance: white solid
  • Application: Ionic liquid
  • DeliveryTime: Within 3 days after payment
  • PackAge: Fluorinated bottle or Drum
  • Port: Chinese Main Port
  • ProductionCapacity: 110 Kilogram/Month
  • Purity: 98%
  • Storage: Keep in cool and dry place
  • Transportation: by air or by sea
  • LimitNum: 1 Kilogram
  • MW: 95.53
  • EINECS: 200-002-3

Superiority

Career Henan Chemical  focus on high complex new type intermediates and fine chemical custom synthesis,scale-up production and rare chemicals. Product category including intermediates&api,catalyst and electronic chemicals. 

We have our R&D team and can supply custom made service for chemicals , and keep good relationship with some pharmaceutical companies. Our synthesis level is well-known to the industry, the products are exported to US, France,Poland,Czech,Ukraine,Spain,Switzerland etc. 

Henan Coreychem Co., Ltd, facing global High-tech pharmaceutical raw materials, high complex new type intermediates, fine chemicals custom synthesis, scale-up production and Rare chemicals trade. Corey have well-equipped machine, strong technical force and considerate marketing team service. We also have rich experience advantage in basic research, small scale process development, scale-up, industrial technology development & production and cost control.

 

Details

Guanidine hydrochloride Basic information
description Protein Denaturation Uses Drug intermediates Preparation Reference quality standards References
Product Name: Guanidine hydrochloride
Synonyms: guanidine,monohydrochloride;guanidinechloride;Guanidinemonohydrochloride;guanidiniumhydrochloride;AMINOFORMAMIDINE HCL;AMINOFORMAMIDINE HYDROCHLORIDE;AMINOMETHANAMIDINE HCL;AMINOMETHANAMIDINE HYDROCHLORIDE
CAS: 50-01-1
MF: CH6ClN3
MW: 95.53
EINECS: 200-002-3
Product Categories: proteinmod;Inhibitors;-;Pharmaceutical Intermediates;Miscellaneous Biochemicals
Mol File: 50-01-1.mol
Guanidine hydrochloride Structure
 
Guanidine hydrochloride Chemical Properties
Melting point  180-185 °C(lit.)
density  1.18 g/mL at 25 °C(lit.)
refractive index  n20/D 1.465
storage temp.  Store at RT.
solubility  H2O: 6 M, clear, colorless
form  Crystals
color  White to slightly yellow
PH 4.5-5.5 (100g/l, H2O, 20℃)
Water Solubility  2280 g/L (20 ºC)
Sensitive  Hygroscopic
λmax λ: 260 nm Amax: 0.040
λ: 280 nm Amax: 0.025
Merck  14,4562
BRN  3591990
Stability: Stable. Hygroscopic. Incompatible with strong oxidizing agents.
CAS DataBase Reference 50-01-1(CAS DataBase Reference)
EPA Substance Registry System Guanidine, monohydrochloride(50-01-1)
 
Safety Information
Hazard Codes  Xn,Xi
Risk Statements  22-36/38
Safety Statements  26-36-22
WGK Germany  1
RTECS  MF4300000
3-10
TSCA  Yes
HS Code  29252000
Toxicity LD50 orally in Rabbit: 655.3 - 907.1 mg/kg LD50 dermal Rabbit > 2000 mg/kg
Guanidine hydrochloride Usage And Synthesis
description Guanidine hydrochloride is a strong organic base existing primarily as guanidium ions at physiological pH. It is found in the urine as a normal product of protein metabolism. It is also used in laboratory research as a protein denaturant.It is also used in the treatment of myasthenia and as a fluorescent probe in HPLC.
Guanidine Hydrochloride is the hydrochloride salt form of guanidine, a strong basic compound with parasympathomimetic activity. Guanidine hydrochloride enhances the release of acetylcholine following a nerve impulse and potentiates acetylcholine actions on muscarinic and nicotinic receptors. It also appears to slow the rates of depolarization and repolarization of muscle cell membranes.
Guanidine Hydrochloride is a powerful, chaotropic agent which is widely used for purification of proteins and nucleic acids. Guanidine Hydrochloride is useful for denaturation and refolding of proteins as well as in the recovery of periplasmic proteins and isolation of RNA. At higher concentrations, this strong denaturant has been reported to solubilize denatured insoluble proteins such as inclusion bodies. When utilized at lower concentrations, Guanidine Hydrochloride is noted to be useful in prompting the refolding of denatured proteins. Guanidine Hydrochloride is also been reported to allow return of enzymatic activity in protocols using Guanidine Hydrochloride as a first step. Guanidine Hydrochloride is an inhibitor of RNase.
Guanidine hydrochloride is used for purification of proteins and nucleic acids. It can be used as a medicine, organic synthesis intermediate and is used in dyes. It acts as an intermediate in the preparation of sulfadiazine, which is an important raw material for sulfamethyldiazine, sulfamethazine and folic acid. It is utilized in the synthesis of 2-amino-pyrimidine, 2-amino-6-methyl-pyrimidine and 2-amino-4,6-dimethyl-pyrimidine. Also used in RNA isolation to dissociate nucleoproteins and inhibit RNase.
Protein Denaturation Guanidine Hydrochloride (GdnHCl) is a better denaturant than urea.It should normally give higher and lower values for m and for Cm, respectively, but identical deltaG° values. Since m values in both denaturants can be predicted/estimated from the size of the protein (Myers et al., 1995) and delatG° should not change, yes it is possible-in principle-to predict Cm in one denaturant, knowing its value in the other.
but to have a general correlation co-efficient is almost impossible as every protein has unique folding. Though such co-relation may be found for a special protein fold, but what purpose it may serve apart from giving a tentative idea that GdnHCl or urea may be a better denaturant! If you are looking for even better denaturant than Gdn HCl then use GdnSCN, it is better and more effective.
Uses Guanidine hydrochloride is used in RNA isolation to dissociate nucleoproteins and inhibit RNase. 
Strong chaotropic agent useful for the denaturation and subsequent refolding of proteins. This strong denaturant can solubilize insoluble or denatured proteins such as inclusion bodies. This can be used as the first step in refolding proteins or enzymes into their active form. Urea and dithiothreitol (DTT) may also be necessary.
Drug intermediates Guanidine hydrochloride drug used primarily as an intermediate in the manufacture of sulfadiazine, an important raw material sulfamethyldiazine, sulfamethazine and folic acid.
Guanidine hydrochloride (or guanidine nitrate) and ethyl cyanoacetate reaction, cyclization of 2,4-diamino-6-hydroxy pyrimidine, folic acid for the synthesis of antianemic. Furthermore guanidine hydrochloride also used synthetic anti-static agent.
Preparation In Dicyanodiamide and ammonium (Ammonium chloride) as raw material, melt reaction at 170-230 ℃, guanidine hydrochloride obtained crude, refined products.
Reference quality standards Name of Project Specifications 
Pharmaceutical grade industrial grade
Appearance white crystal; white crystal
Content > 99% 99.5%
Ammonium <0.3% 0.5%
Water Insoluble substance <0.1% 0.1%
Moisture <0.3% 0.3%
Ash <0.05% 0.05%
Water-soluble test qualified; qualified
Melting range °C 184-188; 182-188
Absorbance (UV wavelength 260NM) <=0.04
Absorbance (UV wavelength 280NM) <=0.02
PH value (4% aqueous solution) 6.4 ± 0.2 6.4 ± 0.2
References #
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Chemical Properties White cryst. powder
Uses cholinergic
Uses Guanidine has a good bacterial and fungicidal efficacy when used in low concentration and can also be used as disinfectant.
Uses Used to synthesis medicine, pesticide, dye and other organic compound, is the important material to make sulfanilamide medicine and folacin, and can be used as anti-static agent of compound fibre.
Definition ChEBI: An aminocarboxamidine, the parent compound of the guanidines.
Hazard Toxic by ingestion, evolves hydrogen chloride fumes on heating.
Purification Methods Crystallise the hydrochloride from hot methanol by chilling to about -10o, with vigorous stirring. The fine crystals are filtered through fritted glass, washed with cold (-10o) methanol, dried at 50o under vacuum for 5hours. (The product is purer than that obtained by crystallisation at room temperature from methanol by adding large amounts of diethyl ether.) [Kolthoff et al. J Am Chem Soc 79 5102 1957, Beilstein 3 H 86, 3 II 71, 3 III 160, 3 IV 150.]

 

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