ChemicalBook--->CAS DataBase List--->56-10-0

56-10-0

56-10-0 Structure

56-10-0 Structure
IdentificationMore
[Name]

2-(2-Aminoethyl)isothiourea dihydrobromide
[CAS]

56-10-0
[Synonyms]

2-(2-AMINOETHYL)-2-THIOPSEUDO-UREA 2HBR
2-(2-AMINOETHYL)-2-THIOPSEUDOUREA DIHYDROBROMIDE
2-(2-aminoethyl)isothiourea dihydrobromide
2-AMINOETHYL CARBAMIMIDOTHIOATE, DIHYDROBROMIDE
2-AMINOETHYL IMIDOTHIOCARBAMATE DIHYDROBROMIDE
2-AMINOETHYLISOTHIOURONIUM BR
2-AMINOETHYLISOTHIOURONIUM BROMIDE
2-AMINOETHYLISOTHIOURONIUM BROMIDE HYDROBROMIDE
AET
AET, DIHYDROBROMIDE
ANTIRADON
BETA-AMINOETHYLISOTHIOURONIUM BROMIDE HYDROBROMIDE
CARBAMIMIDOTHIOIC ACID 2-AMINOETHYL ESTER DIHYDROBROMIDE
IFLAB-BB F0861-0023
NSC 22877
S-(2-AMINOETHYL)ISOTHIOUREA 2HBR
S-(2-AMINOETHYL)ISOTHIOUREA DIHYDROBROMIDE
S-(2-AMINOETHYL)ISOTHIOURONIUM BROMIDE HYDROBROMIDE
S-(2-AMINOETHYL)ISOTHIOURONIUM HYDROGEN-BROMIDE
S(-2-AMINOETHYL)-ITU DIHYDROBROMIDE
[EINECS(EC#)]

200-257-0
[Molecular Formula]

C3H11Br2N3S
[MDL Number]

MFCD00037011
[Molecular Weight]

281.01
[MOL File]

56-10-0.mol
Chemical PropertiesBack Directory
[Melting point ]

190-196 °C(lit.)
[density ]

1.94 g/cm3
[storage temp. ]

Store below +30°C.
[solubility ]

50g/l
[form ]

powder to crystal
[color ]

White to Almost white
[Water Solubility ]

almost transparency
[Merck ]

14,178
[BRN ]

3911163
[InChI]

InChI=1S/C3H9N3S.2BrH/c4-1-2-7-3(5)6;;/h1-2,4H2,(H3,5,6);2*1H
[InChIKey]

XDVMCVGTDUKDHL-UHFFFAOYSA-N
[SMILES]

S(CCN)C(=N)N.Br.Br
[CAS DataBase Reference]

56-10-0(CAS DataBase Reference)
[EPA Substance Registry System]

56-10-0(EPA Substance)
Questions And AnswerBack Directory
[?Synthesis]

Ethylamine thiourea is synthesized by using cycloethylamine, hydrobromic acid and thiourea as raw materials: firstly, thiourea is mixed with hydrogen bromide acid, and cycloethylamine is added dropwise at a temperature below 150 °C. After the reaction is completed, add activated carbon to filter, and then reduce Dehydration under pressure, crystals are precipitated when the temperature is below 50°C, filtered, and washed twice with absolute ethanol.
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

R22:Harmful if swallowed.
R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37:Wear suitable protective clothing and gloves .
S22:Do not breathe dust .
[WGK Germany ]

3
[RTECS ]

UM0175000
[F ]

10-21
[TSCA ]

Yes
[HS Code ]

2930 90 98
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Acute Tox. 4 Oral
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
[Toxicity]

LD50 in mice (mg/kg): 100 i.v., 280 s.c., 480 i.p., 1600 orally (Pospisil)
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Hydrogen bromide-->Monoethanolamine-->Ethyleneimine-->2-Bromoethylamine hydrobromide
Hazard InformationBack Directory
[Description]

S-(2-aminoethyl) Isothiourea is a non-selective inhibitor of all NOS isoforms. For human nNOS, eNOS, and iNOS, the Ki values are 1.8, 2.1, and 0.59 μM, respectively.
[Chemical Properties]

Crystals, hygroscopic.
[Uses]

NOS inhibitor
[in vivo]

AE-ITU dihydrobromide (1 mg/kg/h, i.v., for 1 hour) attenuates the delayed hypotension and vascular hyporeactivity, ameliorates liver dysfunction in LPS (HY-D1056)-administrated Wistar rats[1].

Animal Model:LPS (HY-D1056)-administrated Wistar rats[1]
Dosage:1 mg/kg
Administration:i.v., 1 mg/kg/h for 1 hour
Result:Reduced the serum levels of bilirubin, serum nitrite, GOT, GPT and γGT caused by LPS, inhibited iNOS in lung and liver homogenates.
[IC 50]

iNOS
[Purification Methods]

Crystallise the salt from absolute EtOH/ethyl acetate or MeOH. Store dry as it is hygroscopic in a humid atmosphere. It is a radioprotective agent. When refluxed in EtOH for 16hours or H2O for 30minutes, it decomposes to 2-amino-4(5H)-thiazoline hydrobromide which on recrystallisation from isoPrOH/EtOAc has m 175-176o [Doherty et al. J Am Chem Soc 79 5667 1957].
[References]

[1]. garvey ep, oplinger ja, tanoury gj, et al. potent and selective inhibition of human nitric oxide synthases. inhibition by non-amino acid isothioureas. j biol chem. 1994 oct 28;269(43):26669-76.
Spectrum DetailBack Directory
[Spectrum Detail]

2-(2-Aminoethyl)isothiourea dihydrobromide(56-10-0)MS
2-(2-Aminoethyl)isothiourea dihydrobromide(56-10-0)1HNMR
2-(2-Aminoethyl)isothiourea dihydrobromide(56-10-0)13CNMR
2-(2-Aminoethyl)isothiourea dihydrobromide(56-10-0)IR1
2-(2-Aminoethyl)isothiourea dihydrobromide(56-10-0)IR2
2-(2-Aminoethyl)isothiourea dihydrobromide(56-10-0)Raman
Well-known Reagent Company Product InformationBack Directory
[Alfa Aesar]

S-(2-Aminoethyl)isothiourea dihydrobromide, 98%(56-10-0)
[Sigma Aldrich]

56-10-0(sigmaaldrich)
[TCI AMERICA]

S-(2-Aminoethyl)isothiouronium Bromide Hydrobromide,>98.0%(T)(56-10-0)
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