Buformin hydrochloride structure, CAS 1190-53-0

Buformin hydrochloride

CAS Number1190-53-0

SynonymsEINECS 214-723-6; butyl-biguanide hydrochloride

Molecular FormulaC6H16N5Cl1

Molecular Weight193.68

Purity98.00%

Density

Boiling Point322.7ºC at 760 mmHg

Melting Point174-177ºC

Flash Point

Appearance

EINECS

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Symbol

Signal Word

Cat. No.: 2A-9026405 Purity: 98.00%
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Quality Control of [ 1190-53-0 ] Purity: 98.00% SDS Specification MoL

Chemical & Physical Properties
CAS Number1190-53-0
Catalog No.2A-9026405
Chinese Name丁双胍盐酸盐
SynonymsEINECS 214-723-6; butyl-biguanide hydrochloride
Molecular FormulaC6H16N5Cl1
Molecular Weight193.68
Purity98.00
Boiling Point322.7ºC at 760 mmHg
Melting Point174-177ºC
Storage Condition1. The warehouse is ventilated and dried at low te
ApplicationBuformin hydrochloride (1-Butylbiguanide hydrochloride) is a potent, orally active antidiabetic agent and an AMPK activator. Buformin decreases hepatic gluconeogenesis and decreases glycemia. Buformin
HTC2925290090
PubChem ID555148
MDL NumberMFCD00045591
SMILESCCCCN=C(N)N=C(N)N.Cl
InChIInChI=1S/C6H15N5.ClH/c1-2-3-4-10-6(9)11-5(7)8;/h2-4H2,1H3,(H6,7,8,9,10,11);1H
InChI KeyKKLWSPPIRBIEOV-UHFFFAOYSA-N
MSDSmsds/26405_1_1190_53_0.pdf
Use ofBuformin hydrochloride (1-Butylbiguanide hydrochloride) is a potent and orally active biguanide antidiabetic agent, an AMPK activator. Buformin hydrochloride decreases hepatic gluconeogenesis and lowers blood glucose production in vivo. Buformin hydrochloride also has anti-cancer activities and is applied in cancer study (such as, cervical cancer and breast cancer, et al)[1]. Properties Name Buformin Hydrochloride Synonym More Synonyms Buformin hydrochloride Biological Activity Description Buformin hydrochloride (1-Butylbiguanide hydrochloride) is a potent and orally active biguanide antidiabetic agent, an AMPK activator. Buformin hydrochloride decreases hepatic gluconeogenesis and lowers blood glucose production in vivo. Buformin hydrochloride also has anti-cancer activities and is applied in cancer study (such as, cervical cancer and breast cancer, et al)[1]. Related Catalog Signaling Pathways >> Epigenetics >> AMPK Research Areas >> Cancer Signaling Pathways >> PI3K/Akt/mTOR >> AMPK References [1]. Amanda B Parris, et al. Buformin hydrochloride Inhibits the Stemness of erbB-2-overexpressing Breast Cancer Cells and Premalignant Mammary Tissues of MMTV-erbB-2 Transgenic Mice. J Exp Clin Cancer Res [2]. Jing Li, et al. Buformin hydrochloride Suppresses Proliferation and Invasion via AMPK/S6 Pathway in Cervical Cancer and Synergizes With Paclitaxel. Cancer Biol Ther. 2018 Jun 3;19(6):507-517. Chemical & Physical Properties Exact Mass 193.10900 PSA 97.78000 LogP 2.27750 InChIKey KKLWSPPIRBIEOV-UHFFFAOYSA-N SMILES CCCCN=C(N)N=C(N)N.Cl Toxicological Information CHEMICAL IDENTIFICATION RTECS NUMBER : CHEMICAL NAME : Biguanide, 1-butyl-, monohydrochloride CAS REGISTRY NUMBER : LAST UPDATED : DATA ITEMS CITED : MOLECULAR FORMULA : MOLECULAR WEIGHT : WISWESSER LINE NOTATION : MUYZMYUM&M4 &GH HEALTH HAZARD DATA ACUTE TOXICITY DATA TYPE OF TEST : LD50 - Lethal dose, 50 percent kill ROUTE OF EXPOSURE : SPECIES OBSERVED : Rodent - rat DOSE/DURATION : TOXIC EFFECTS : Details of toxic effects not reported other than lethal dose value TYPE OF TEST : LD50 - Lethal dose, 50 percent kill ROUTE OF EXPOSURE : SPECIES OBSERVED : Rodent - mouse DOSE/DURATION : TOXIC EFFECTS : Details of toxic effects not reported other than lethal dose value TYPE OF TEST : LD50 - Lethal dose, 50 percent kill ROUTE OF EXPOSURE : Intraperitoneal SPECIES OBSERVED : Rodent - mouse DOSE/DURATION : TOXIC EFFECTS : Behavioral - somnolence (general depressed activity) Behavioral - convulsions or effect on seizure threshold Lungs, Thorax, or Respiration - respiratory stimulation TYPE OF TEST : LD50 - Lethal dose, 50 percent kill ROUTE OF EXPOSURE : Intravenous SPECIES OBSERVED : Rodent - mouse DOSE/DURATION : TOXIC EFFECTS : Details of toxic effects not reported other than lethal dose value TYPE OF TEST : LD50 - Lethal dose, 50 percent kill ROUTE OF EXPOSURE : SPECIES OBSERVED : Rodent - guinea pig DOSE/DURATION : TOXIC EFFECTS : Details of toxic effects not reported other than lethal dose value TYPE OF TEST : LD50 - Lethal dose, 50 percent kill ROUTE OF EXPOSURE : Subcutaneous SPECIES OBSERVED : Rodent - guinea pig DOSE/DURATION : TOXIC EFFECTS : Details of toxic effects not reported other than lethal dose value MUTATION DATA TYPE OF TEST : Cytogenetic analysis TEST SYSTEM : Human Embryo DOSE/DURATION : REFERENCE : SNSHBT Senshokutai. Chromosome. (Sensyokutai Gakkai, Kaokusai Kirisutokyo Daigaku, Mitaka, Tokyo-to, Japan) No.1- 1946- Adopted new numbering in 1976. Volume(issue)/page/year: (20),574,1980 Safety Information GHS05, GHS07 Signal Word Danger Hazard Statements H302-H315-H318-H335 Precautionary Statements P280-P301 + P312 + P330-P305 + P351 + P338 + P310 Hazard Codes Xi Risk Phrases 22-43-36 RIDADR NONH for all modes of transport HS Code 2925290090
Tax Rebate9.0%
Supervisionnone
Transport InfoProduct name: Summary 2925290090 other imines and their derivatives; salts thereof. Supervision conditions:None. VAT: 17.0%. Tax rebate rate:9.0%. MFN tariff: 6.5%. General tariff:30.0%
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