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1,3-Diaminoguanidine monohydrochloride - 97%, high purity , CAS No.36062-19-8

≥97%

CAS#: 36062-19-8
Formula: CH₇N₅·HCl
Molecular Weight: 125.56
Beilstein Registry Number: 3(4)241
EC Number: 252-854-0
MDL number: MFCD00012948
PubChem CID: 9566041
PubChem SID: 488196279

Item Number

D109093

Grouped product items
SKU	Size	Availability	Price
D109093-5g	5g	In stock	$25.90
D109093-10g	10g	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$46.90
D109093-25g	25g	Available within 1-2 weeks(?) Item is derived from our semi-finished stock and is processed in 1-2 weeks.	$73.90
D109093-100g	100g	In stock	$263.90
D109093-500g	500g	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$1,185.90

View related series

Functional group compounds Guanidines

Basic Description

Synonyms	1,3-Diaminoguanidine monohydrochloride\|36062-19-8\|1,3-Diaminoguanidine hydrochloride\|N,N'-DIAMINOGUANIDINE\|Carbonimidic dihydrazide, hydrochloride\|n,n'-diaminoguanidine monohydrochloride\|38360-74-6\|014Y506OEG\|Carbonimidic dihydrazide monohydrochloride\|Car
Specifications & Purity	97%
Shipped In	Normal
Product Description	1,3-Diaminoguanidine monohydrochloride undergoes condensation reaction with: · 4-isothiocyanato-4-methylpentane-2-one to yield condensed pyrimidines · various aldehydes and ketones to yield bis guanidine derivatives N,N'-Diaminoguanidine Monohydrochloride is an analyte for HPLC. It also functions as an intermediate for the synthesis of energetic salts or materials based on dinitroguanidine.

Names and Identifiers

Pubchem Sid	488196279
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/488196279
IUPAC Name	1,2-diaminoguanidine;hydrochloride
INCHI	InChI=1S/CH7N5.ClH/c2-1(5-3)6-4;/h3-4H2,(H3,2,5,6);1H
InChi Key	HAZRIBSLCUYMQP-UHFFFAOYSA-N
Canonical SMILES	C(=NN)(N)NN.Cl
Isomeric SMILES	C(=N\N)(\N)/NN.Cl
WGK Germany	3
PubChem CID	9566041
Molecular Weight	125.56
Beilstein	3(4)241
Reaxy-Rn	3556702

Certificates

Certificate of Analysis(COA)

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7 results found

Lot Number	Certificate Type	Date	Item
J1908148	Certificate of Analysis	Jul 14, 2023	D109093
B1918048	Certificate of Analysis	Dec 09, 2022	D109093
D2425019	Certificate of Analysis	Jun 09, 2022	D109093
F2220412	Certificate of Analysis	Jun 09, 2022	D109093
F2220413	Certificate of Analysis	Jun 09, 2022	D109093
F2220414	Certificate of Analysis	Jun 09, 2022	D109093
I2321050	Certificate of Analysis	Jun 09, 2022	D109093

Solubility

water: soluble 50 mg/mL, clear to very slightly hazy, colorless to faintly yellow

Sensitivity

Moisture sensitive

Melt Point(°C)

180-182°C

Safety and Hazards(GHS)

Pictogram(s)	GHS07
Signal	Warning
Hazard Statements	H315:Causes skin irritation H319:Causes serious eye irritation H335:May cause respiratory irritation
Precautionary Statements	P261:Avoid breathing dust/fume/gas/mist/vapors/spray. P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses if present and easy to do - continue rinsing. P280:Wear protective gloves/protective clothing/eye protection/face protection. P302+P352:IF ON SKIN: wash with plenty of water. P321:Specific treatment (see ... on this label). P405:Store locked up. P501:Dispose of contents/container to ... P264:Wash hands [and …] thoroughly after handling. P271:Use only outdoors or in a well-ventilated area. P304+P340:IF INHALED: Remove person to fresh air and keep comfortable for breathing. P403+P233:Store in a well-ventilated place. Keep container tightly closed. P362+P364:Take off contaminated clothing and wash it before reuse. P264+P265:Wash hands [and …] thoroughly after handling. Do not touch eyes. P337+P317:If eye irritation persists: Get medical help. P332+P317:If skin irritation occurs: Get medical help. P319:Get medical help if you feel unwell.
WGK Germany	3
Reaxy-Rn	3556702

References

1. K Kumari,S Umar,V Bansal,M K Sahib. (1991-08-01) Inhibition of diabetes-associated complications by nucleophilic compounds.. Diabetes, 40 ((8)): (1079-1084). [PMID:1907249]
2. K Hasan,B J Heesen,J A Corbett,M L McDaniel,K Chang,W Allison,B H Wolffenbuttel,J R Williamson,R G Tilton. (1993-11-02) Inhibition of nitric oxide formation by guanidines.. European journal of pharmacology, 249 ((1)): (101-106). [PMID:7506664]
3. D J Wolff,A Lubeskie. (1996-01-15) Inactivation of nitric oxide synthase isoforms by diaminoguanidine and NG-amino-L-arginine.. Archives of biochemistry and biophysics, 325 ((2)): (227-234). [PMID:8561501]
4. J Brimnes,H Miörner,U Anthoni,L Bruun,G Houen. (1999-06-24) Reactions of N-N and N-O compounds with horseradish peroxidase and peroxidases from Mycobacterium tuberculosis.. APMIS : acta pathologica, microbiologica, et immunologica Scandinavica, 107 ((6)): (555-565). [PMID:10379683]
5. Naoyoshi Ishikawa,Toshio Miyata,Yasuhiko Ueda,Reiko Inagi,Yuko Izuhara,Hiroko Yuzawa,Hiroshi Onogi,Makoto Nishina,Masaomi Nangaku,Charles Van Ypersele De Strihou,Kiyoshi Kurokawa. (2002-12-11) Affinity adsorption of glucose degradation products improves the biocompatibility of conventional peritoneal dialysis fluid.. Kidney international, 63 ((1)): (331-339). [PMID:12472800]
6. María Paula Campestre,Cesar Daniel Bordenave,Andrea Cecilia Origone,Ana Bernardina Menéndez,Oscar Adolfo Ruiz,Andrés Alberto Rodríguez,Santiago Javier Maiale. (2011-02-18) Polyamine catabolism is involved in response to salt stress in soybean hypocotyls.. Journal of plant physiology, 168 ((11)): (1234-1240). [PMID:21324548]
7. D Dvornik,T C Hohman,M D Basso. (1996-01-01) Aminoguanidine does not inhibit aldose reductase activity in galactose-fed rats.. Journal of diabetes and its complications, 10 ((1)): (23-30). [PMID:8639971]
8. Anthony J Lee,Kathleen R Noon,Suree Jianmongkol,Miranda Lau,Gary J Jenkins,Yoichi Osawa. (2005-12-20) Metabolism of aminoguanidine, diaminoguanidine, and NG-amino-L-arginine by neuronal NO-synthase and covalent alteration of the heme prosthetic group.. Chemical research in toxicology, 18 ((12)): (1927-1933). [PMID:16359183]

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