N-Hydroxybenzenecarboximidamide

Modify Date: 2025-08-20 10:00:48

N-Hydroxybenzenecarboximidamide structure	Common Name	N-Hydroxybenzenecarboximidamide
	CAS Number	613-92-3	Molecular Weight	136.151
	Density	1.2±0.1 g/cm3	Boiling Point	307.4±25.0 °C at 760 mmHg
	Molecular Formula	C₇H₈N₂O	Melting Point	77°C
	MSDS	Chinese USA	Flash Point	139.7±23.2 °C
	Symbol	GHS06	Signal Word	Danger

Name	benzamidoxime
Synonym	More Synonyms

Density	1.2±0.1 g/cm3
Boiling Point	307.4±25.0 °C at 760 mmHg
Melting Point	77°C
Molecular Formula	C₇H₈N₂O
Molecular Weight	136.151
Flash Point	139.7±23.2 °C
Exact Mass	136.063660
PSA	58.61000
LogP	1.15
Vapour Pressure	0.0±0.7 mmHg at 25°C
Index of Refraction	1.574
InChIKey	MXOQNVMDKHLYCZ-UHFFFAOYSA-N
SMILES	NC(=NO)c1ccccc1

N-Hydroxybenzenecarboximidamide MSDS(Chinese)

CHEMICAL IDENTIFICATION

RTECS NUMBER :: CV6920000

CHEMICAL NAME :: Benzamidoxime

CAS REGISTRY NUMBER :: 613-92-3

LAST UPDATED :: 199709

DATA ITEMS CITED :: 2

MOLECULAR FORMULA :: C7-H8-N2-O

MOLECULAR WEIGHT :: 136.17

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

MUTATION DATA

TYPE OF TEST :: DNA damage

TEST SYSTEM :: Rodent - rat Liver

DOSE/DURATION :: 5 umol/L

REFERENCE :: JCROD7 Journal of Cancer Research and Clinical Oncology. (Springer-Verlag New York, Inc., Service Center, 44 Hartz Way, Secaucus, NJ 07094) V.93- 1979- Volume(issue)/page/year: 111,123,1986

Symbol	GHS06
Signal Word	Danger
Hazard Statements	H301-H315-H319-H335
Precautionary Statements	P261-P301 + P310-P305 + P351 + P338
Hazard Codes	Xn:Harmful;
Risk Phrases	R20/21/22;R36/37/38
Safety Phrases	S22-S36/37/39
RIDADR	2811
RTECS	CY6920000
HS Code	2925290090

HS Code	2925290090
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%

A novel and specific fluorescence reaction for uracil.

Anal. Chim. Acta 674(2) , 234-8, (2010)

Facile and specific methods to quantify a nucleobase in biological samples are of great importance for diagnosing disorders in nucleic acid metabolism. In the present study, a novel fluorogenic reacti...

Characteristics of the microsomal N-hydroxylation of benzamidine to benzamidoxime.

Xenobiotica 17(6) , 659-67, (1987)

1. A simple and fast h.p.l.c. analysis of benzamidoxime formed by microsomal N-hydroxylation of benzamidine is presented which is well suited for the determination of the N-oxygenation activity of mic...

Biotransformation of benzamidine and benzamidoxime in vivo.

Arch. Pharm. (Weinheim) 326(10) , 807-12, (1993)

After administration of benzamidine (1) or benzamidoxime (2), respectively, to rats and rabbits, plasma from rats and rabbits as well as urine from rats were examined for the presence of benzamidoxime...

Name: Induction of NO release in phosphate buffer pH 7.4 containing 0.5 mM L-cysteine asses...
Source: ChEMBL
Target: N/A
External Id: CHEMBL1641183

Name: Induction of NO release in phosphate buffer pH 7.4 containing 0.5 mM thiophenol asses...
Source: ChEMBL
Target: N/A
External Id: CHEMBL1641184

Name: Substrate activity at human mARC1 expressed in Escherichia coli assessed as turnover ...
Source: ChEMBL
Target: Mitochondrial amidoxime-reducing component 1
External Id: CHEMBL4614164

Name: Antioxidant activity assessed as DPPH free radical scavenging activity at 50 uM after...
Source: ChEMBL
Target: N/A
External Id: CHEMBL1641174

Name: Antioxidant activity assessed as DPPH free radical scavenging activity at 100 uM afte...
Source: ChEMBL
Target: N/A
External Id: CHEMBL1641175

Name: Nitric oxide (NO) formation during oxidation of NADPH and O2, catalyzed by NOS II det...
Source: ChEMBL
Target: Nitric oxide synthase, inducible
External Id: CHEMBL748041

Name: Antioxidant activity assessed as DPPH free radical scavenging activity at 100 uM afte...
Source: ChEMBL
Target: N/A
External Id: CHEMBL1641177

Name: Ability to undergo a P450-dependent oxidative cleavage of the C=N bond by incubating ...
Source: ChEMBL
Target: Rattus norvegicus
External Id: CHEMBL783918

Name: Substrate activity at human mARC1 expressed in Escherichia coli assessed as turnover ...
Source: ChEMBL
Target: Mitochondrial amidoxime-reducing component 1
External Id: CHEMBL4614174

Name: Ability to undergo a P450-dependent oxidative cleavage of the C=N bond by incubating ...
Source: ChEMBL
Target: Rattus norvegicus
External Id: CHEMBL783919

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EINECS 210-361-8

BENZAMIDE OXIME

benzohydroxamamide

Benzamidoxim

MFCD06656049

N-Hydroxybenzenecarboximidamide

N'-hydroxybenzimdamide

benzenylaminoxime

benzamidoxide

N'-hydroxy-benzene-carboximidamide

BENZAMIDOXIME

N-Hydroxybenzamidine

Benzamidoxine

benzenylamidoxime

BENZAMIDOXIME HYDROCHLORIDE

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Shanghai Nianxing Industrial Co., Ltd
China
Product Name: N-Hydroxybenzenecarboximidamide
Price: Check
Purity: 98.0%
Delivery: 10 Day
Contact: Yang
Email: sales@echemcloud.com

Dayang Chem (Hangzhou) Co., Ltd.
China
Product Name: Benzamide oxime
Price: $Inquiry/100g $Inquiry/1kg $Inquiry/100kg $Inquiry/1000kg
Purity: 98.0%
Delivery: Inquiry
Contact: Ms Wang
Email: enquiry@dycnchem.com

Shanghai Jizhi Biochemical Technology Co., Ltd
China
Product Name: N-Hydroxybenzenecarboximidamide
Price: ￥1748.0/25g
Purity: 98.0%
Delivery: 2 Day
Contact: Liu jia
Email: 2130147988@qq.com

Henan Tianfu Chemical Co., Ltd.
China
Product Name: BENZAMIDOXIME HYDROCHLORIDE 613-92-3
Price: $Inquiry/1kg $Inquiry/25kg $Inquiry/1000kg $Inquiry/10ton
Purity: 99.0%
Delivery: Inquiry
Contact: Anson
Email: info@tianfuchem.com

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N-Hydroxybenzenecarboximidamide

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ACUTE TOXICITY DATA

MUTATION DATA

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N-HydroxybenzenecarboximidamideBioassay

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The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.