Cupferron

Modify Date: 2024-01-03 12:48:03

Cupferron Structure
Cupferron structure
Common Name Cupferron
CAS Number 135-20-6 Molecular Weight 155.155
Density N/A Boiling Point 243.8ºC at 760 mmHg
Molecular Formula C6H9N3O2 Melting Point 150-155 °C (dec.)(lit.)
MSDS Chinese USA Flash Point 101.3ºC
Symbol GHS06 GHS08
GHS06, GHS08
Signal Word Danger

 Names

Name Cupferron
Synonym More Synonyms

 Chemical & Physical Properties

Boiling Point 243.8ºC at 760 mmHg
Melting Point 150-155 °C (dec.)(lit.)
Molecular Formula C6H9N3O2
Molecular Weight 155.155
Flash Point 101.3ºC
Exact Mass 155.069473
PSA 55.73000
LogP 2.04840
Vapour Pressure 0.0169mmHg at 25°C
Stability Stable, but may be moisture sensitive. Incompatible with strong oxidizing agents, strong bases, strong acids.
Water Solubility <0.1 g/100 mL at 18.5 ºC

 Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
NC4725000
CHEMICAL NAME :
Hydroxylamine, N-nitroso-N-phenyl-, ammonium salt
CAS REGISTRY NUMBER :
135-20-6
LAST UPDATED :
199706
DATA ITEMS CITED :
18
MOLECULAR FORMULA :
C6-H6-N2-O2.H3-N
MOLECULAR WEIGHT :
155.18
WISWESSER LINE NOTATION :
QNR&NO &ZH

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
Standard Draize test
ROUTE OF EXPOSURE :
Administration into the eye
SPECIES OBSERVED :
Rodent - rabbit
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
199 mg/kg
TOXIC EFFECTS :
Behavioral - muscle weakness Lungs, Thorax, or Respiration - dyspnea Skin and Appendages - dermatitis, other (after systemic exposure)
TYPE OF TEST :
LDLo - Lowest published lethal dose
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
50 mg/kg
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 :
Intravenous
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
180 mg/kg
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 :
Administration onto the skin
SPECIES OBSERVED :
Rodent - guinea pig
DOSE/DURATION :
>5 gm/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
123 gm/kg/78W-C
TOXIC EFFECTS :
Tumorigenic - Carcinogenic by RTECS criteria Vascular - tumors Liver - tumors
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
437 gm/kg/78W-C
TOXIC EFFECTS :
Tumorigenic - Carcinogenic by RTECS criteria Vascular - tumors Liver - tumors
TYPE OF TEST :
TD - Toxic dose (other than lowest)
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
9040 mg/kg/65W-C
TOXIC EFFECTS :
Tumorigenic - equivocal tumorigenic agent by RTECS criteria Lungs, Thorax, or Respiration - tumors
TYPE OF TEST :
Cytogenetic analysis

MUTATION DATA

TYPE OF TEST :
DNA inhibition
TEST SYSTEM :
Human HeLa cell
DOSE/DURATION :
2 mmol/L
REFERENCE :
CRNGDP Carcinogenesis (London). (Oxford Univ. Press, Pinkhill House, Southfield Road, Eynsham, Oxford OX8 1JJ, UK) V.1- 1980- Volume(issue)/page/year: 13,2389,1992 *** NIOSH STANDARDS DEVELOPMENT AND SURVEILLANCE DATA *** NIOSH OCCUPATIONAL EXPOSURE SURVEY DATA : NOHS - National Occupational Hazard Survey (1974) NOHS Hazard Code - A1044 No. of Facilities: 6 (estimated) No. of Industries: 1 No. of Occupations: 1 No. of Employees: 23 (estimated) NOES - National Occupational Exposure Survey (1983) NOES Hazard Code - A1044 No. of Facilities: 10 (estimated) No. of Industries: 1 No. of Occupations: 1 No. of Employees: 136 (estimated) No. of Female Employees: 39 (estimated)

 Safety Information

Symbol GHS06 GHS08
GHS06, GHS08
Signal Word Danger
Hazard Statements H301-H315-H319-H335-H351
Precautionary Statements P261-P281-P301 + P310-P305 + P351 + P338
Personal Protective Equipment Eyeshields;Faceshields;full-face particle respirator type N100 (US);Gloves;respirator cartridge type N100 (US);type P1 (EN143) respirator filter;type P3 (EN 143) respirator cartridges
Hazard Codes T:Toxic;
Risk Phrases R25;R36/37/38;R40
Safety Phrases S26-S36/37-S45
RIDADR UN 2811 6.1/PG 3
WGK Germany 3
RTECS NC4725000
Packaging Group III
Hazard Class 6.1
HS Code 3822009000

 Synthetic Route

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Cupferron Structure

Cupferron

CAS#:135-20-6

Literature: Organic Preparations and Procedures International, , vol. 30, # 4 p. 439 - 446

~%

Cupferron Structure

Cupferron

CAS#:135-20-6

Literature: Organic Preparations and Procedures International, , vol. 30, # 4 p. 439 - 446

~%

Cupferron Structure

Cupferron

CAS#:135-20-6

Literature: Journal of the Chemical Society, , vol. 117, p. 589

~%

Cupferron Structure

Cupferron

CAS#:135-20-6

Literature: J.ind.eng.Chem., , vol. 12, p. 799 Chem. Zentralbl., , vol. 91, # IV p. 662

 Customs

HS Code 2928000090
Summary 2928000090 other organic derivatives of hydrazine or of hydroxylamine VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:20.0%

 Articles26

More Articles
Intermediate analogue inhibitors of mandelate racemase: N-Hydroxyformanilide and cupferron.

Bioorg. Med. Chem. Lett. 17 , 105-8, (2007)

Mandelate racemase (MR) catalyzes the 1,1-proton transfer that interconverts the enantiomers of mandelate. The transition state/intermediate analogues N-hydroxyformanilide (K(i)=2.79+/-0.19 microM) an...

Celecoxib prodrugs possessing a diazen-1-ium-1,2-diolate nitric oxide donor moiety: synthesis, biological evaluation and nitric oxide release studies.

Bioorg. Med. Chem. Lett. 20 , 4544-9, (2010)

A new class of anti-inflammatory (AI) cupferron prodrugs was synthesized wherein a diazen-1-ium-1,2-diolato ammonium salt, and its O(2)-methyl and O(2)-acetoxyethyl derivatives, nitric oxide (NO) dono...

Synthesis and characterization of lithium oxonitrate (LiNO).

J. Inorg. Biochem. 118 , 128-33, (2013)

The oxonitrate(1-) anion (NO(-)), the one-electron reduction product of nitric oxide and conjugate base of HNO, has not been synthesized and isolated due to the inherent reactivity of this anion. The ...

 Synonyms

COPPERONE
CUPEFERRON
Kupferron
Cupferon
N-nitroso-N-phenyl-hydroxylamin,ammonium salt
EINECS 205-183-2
Benzenamine, N-hydroxy-N-nitroso-, ammonium salt
Kupferon
CUPFERRON,ACS
N-hydroxy-N-nitroso-benzenamine,ammonium salt
Ammonium Nitrosophenylhydroxylamine
N-nitrosophenyl hydroxylamine ammonium salt
Ammonium 2-oxo-1-phenylhydrazinolate
MFCD00078422
N-Nitroso-N-phenylhydroxylamine Ammonium Salt
N-Nitroso-N-phenyl-hydroxylamin,Ammonium-Salz
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