CAS 624-82-8|FORMAMIDOXIME

Introduction:Basic information about CAS 624-82-8|FORMAMIDOXIME, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
Common NameFORMAMIDOXIME
CAS Number624-82-8Molecular Weight60.05530
Density1.29g/cm3Boiling Point224ºC at 760 mmHg
Molecular FormulaCH4N2OMelting Point112-115ºC(lit.)
MSDSChineseUSAFlash Point89.3ºC
Symbol
GHS07, GHS08
Signal WordWarning

Names

Nameformamidoxime
SynonymMore Synonyms

Chemical & Physical Properties

Density1.29g/cm3
Boiling Point224ºC at 760 mmHg
Melting Point112-115ºC(lit.)
Molecular FormulaCH4N2O
Molecular Weight60.05530
Flash Point89.3ºC
Exact Mass60.03240
PSA58.61000
LogP0.06290
Index of Refraction1.471
InChIKeyIONSZLINWCGRRI-UHFFFAOYSA-N
SMILESNC=NO
Storage condition2-8°C

Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
LQ4632000
CHEMICAL NAME :
Formamidoxime
CAS REGISTRY NUMBER :
624-82-8
LAST UPDATED :
199304
DATA ITEMS CITED :
2
MOLECULAR FORMULA :
C-H4-N2-O
MOLECULAR WEIGHT :
60.07
WISWESSER LINE NOTATION :
QM1UM

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Subcutaneous
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
350 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
ARZNAD Arzneimittel-Forschung. Drug Research. (Editio Cantor Verlag, Postfach 1255, W-7960 Aulendorf, Fed. Rep. Ger.) V.1- 1951- Volume(issue)/page/year: 18,645,1968

Safety Information

Symbol
GHS07, GHS08
Signal WordWarning
Hazard StatementsH302 + H312 + H332-H351
Precautionary StatementsP280
Personal Protective Equipmentdust mask type N95 (US);Eyeshields;Gloves
Hazard CodesXn
Risk Phrases20/21/22-40
Safety Phrases22-36
RIDADRNONH for all modes of transport
WGK Germany3
RTECSLQ4632000
HS Code2925290090

Customs

HS Code2925290090
Summary2925290090 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%

Articles5

More Articles
Antitumor activity of amidoximes (hydroxyurea analogs) in murine tumor systems.

Cancer Res. 38(5) , 1291-5, (1978)

A series of amidoximes was prepared and evaluated for possible antitumor activity against L1210 leukemia. Three of the most active compounds in the L1210 system, formamidoxime, acetamidoxime, and 2-am...

Nitric oxide synthesis by tracheal smooth muscle cells by a nitric oxide synthase-independent pathway.

Am. J. Physiol. 275(5 Pt 1) , L895-901, (1998)

Nitric oxide (NO) is known to be synthesized from L-arginine in a reaction catalyzed by NO synthase. Liver cytochrome P-450 enzymes also catalyze the oxidative cleavage of C==N bonds of compounds cont...

Effects of phenobarbital, beta-naphthoflavone, dexamethasone, and formamidoxime on the turnover of inducible microsomal proteins in cultured hepatocytes.

J. Biol. Chem. 256(24) , 13079-84, (1981)

Microsomal proteins from cultured chick embryo hepatocytes were separated by polyacrylamide gel electrophoresis and their rate constants of degradation (Kd) were estimated using double isotope techniq...

Synonyms

EINECS 210-865-8
carboxamidoxime
Aminoformaldehyde oxime
formamideoxime
N-hydroxycarboximidamide
n-hydroxy-methanimidamid
formamidoxim
n-hydroxymethanimidamide
isuretin
MFCD00008125
isouretin
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