벤자미딘염산염

Benzamidine, hydrochloride

HCID 80289CAS 1670-14-0

기본 정보

표준 SMILES
Cl.N=C(N)c1ccccc1
InChIKey
LZCZIHQBSCVGRD-UHFFFAOYSA-N
분자식
C7H8N2.ClH
평균 분자량
156.61 g/mol
단동위원소 질량
156.04542597

이름 및 식별자

우선 이름
Benzamidine, hydrochloride
IUPAC
benzenecarboximidamide;hydrochloride
현지명
벤자미딘염산염
영어명
Benzamidine hydrochloride
분자식
C7H9ClN2
분자량
156.61

이름 및 동의어

Benzamidine hydrochloride1670-14-0Benzenecarboximidamide, monohydrochlorideAmidinobenzene hydrochlorideBenzamidine, hydrochlorideBenzamidine, monohydrochlorideAmidinobenzene hydrochloride (1:1)DTXSID9044401Benzenecarboximidamide, hydrochloride (1:1)NSC-20200G112W4L27DTXCID7024401
이름 더 보기
벤자미딘염산염benzamidine hydroxychlorides-dimethylesterBENZAMIDE HCL H2OBenzamidine hydrochlbenzamidiniumchlorideenzamidine hydrochloride
RefChem:563020216-795-4Benzimidamide hydrochlorideBENZAMIDINE HCLBenzenecarboximidamide hydrochlorideBenzamidinium chloride477904-89-5MFCD00013025

데이터베이스 식별자

CAS
1670-14-0
PubChem CID
80289
DTXSID
DTXSID9044401
ChEMBL
CHEMBL537204
UNII
0G112W4L27
EC Number
216-795-4

물성

구조 계산 물성

극성 표면적
49.9 Ų
수소 결합 공여자 수
3
수소 결합 수용자 수
1
회전 가능 결합 수
1
무거운 원자 수
10

실험 및 물리화학적 성질

Chemical ClassesNitrogen Compounds -> Other Aromatics (Nitrogen)
Vapor Pressure0.02 [mmHg]
Physical DescriptionBeige crystalline solid; [Sigma-Aldrich MSDS]

물리화학적 성질

녹는점
86 · 86-88 °C(lit.)
저장 조건
2 · 2-8°C
용해도
25 mg/mlDMSO: · DMF: 25mg/mlDMSO: 25mg/ml에탄올: 10mg/mlPBS(pH 7.2): 3mg/ml
물리적 상태
가루
색상
흰색에서 황백색까지
수소이온지수(pH)
4 to · 4.0 to 6.5(50g/L, 25 ℃)

화학적 성질

white to off-white powder

안전 및 규제

GHS 분류

GHS Classification · 4건

Warning

H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]

P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 166 reports by companies from 12 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

유해성 정보

Regulatory Information · 3건

Chemical: Benzenecarboximidamide, monohydrochloride

Status: Active Update: 24-06-2021 https://echa.europa.eu/registration-dossier/-/registered-dossier/24030

Benzenecarboximidamide, monohydrochloride: Does not have an individual approval but may be used under an appropriate group standard

Hazards SummaryCauses somnolence and lung changes in intraperitoneal lethal-dose studies of mice (LD50 = 580 mg/kg); [RTECS] A skin and strong eye irritant; [Sigma-Aldrich MSDS] See Pentamidine isethionate.
Hazard Classes and CategoriesSkin Irrit. 2 (100%)

안전 데이터

wgk
3
tsca
TSCA listed
rtecs
CV6260000
HS 번호
29252900
risk_code
36/37/38
hazard_code
Xi

화학 및 산업

약리 정보

MeSH Pharmacological ClassificationExogenous or endogenous compounds which inhibit SERINE ENDOPEPTIDASES.

용도 및 제조

General Manufacturing InformationBenzenecarboximidamide, hydrochloride (1:1): ACTIVE
응용 분야 · 2건

개요Benzamidine hydrochloride is a reversible inhibitor of trypsin, trypsin-like enzymes, and serine proteases. A concentration of approximately 1 mM is used for general protease inhibition. To inhibit proteases from yeast, a range of 0.5 to 4.0 mM is used and it is for the most part interchangeable with pepstatin A.In addition to being a strong competitive inhibitor of trypsin, benzamidine HCl has been also shown to be a strong competitive inhibitor of thrombin and plasmin. It was also found to be as effective as aprotinin in the prevention of glucagon degradation in human plasma.

용도Benzamidine is a reversible inhibitor of serine proteases, including trypsin, plasmin, and thrombin (Kis = 35, 350, and 220 μM, respectively). In addition to its use as a general serine protease inhibitor, benzamidine is used, when immobilized, to purify novel proteases.

제조 방법 · 1건

To a stainless steel rocking autoclave equipped with a stirrer is added 103.0 gm (1.0 mole) of benzonitrile, 214.0 gm (4.0 mole) of ammonium chloride, and 306.0 gm (18.0 mole) of ammonia is introduced by means of a transfer bomb. The reaction mixture is heated at 150°C for 18 hr (pressure: 1300-6500 psig), cooled, and, with appropriate precautions for the safe control of the excess ammonia, is vented to atmospheric pressure. The reaction mixture is extracted with ether to remove approximately 5% unreacted benzonitrile, and then extracted with hot acetonitrile or ethanol to separate the amidine hydrochloride from the unreacted ammonium chloride. Concentration of the latter affords 120.5 gm (77%) of benzamidine hydrochloride, m.p. 161-163°C.

공급사50 곳

国药集团化学试剂有限公司86-21-63210123 · [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]
爱斯特(成都)生物制药股份有限公司+86-28-85122536 85324413 · [email protected]

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