<Suppliers Price>

(L)-Canavanine

Names

[ CAS No. ]:
543-38-4

[ Name ]:
(L)-Canavanine

[Synonym ]:
L-Canavanine
L-α-AMINO-γ-[GUANIDINOOXY]-N-BUTYRIC ACID

Biological Activity

[Description]:

L-Canavanine is aamino acids and their derivatives.

[Related Catalog]:

Research Areas >> Others

Chemical & Physical Properties

[ Density]:
1.61g/cm3

[ Boiling Point ]:
431.2ºC at 760mmHg

[ Melting Point ]:
184ºC

[ Molecular Formula ]:
C5H12N4O3

[ Molecular Weight ]:
176.17

[ Flash Point ]:
214.6ºC

[ Exact Mass ]:
176.09100

[ PSA ]:
134.45000

[ LogP ]:
0.09430

[ Index of Refraction ]:
1.602

MSDS

Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
ES7002000
CHEMICAL NAME :
Butyric acid, 2-amino-4-(guanidinooxy)-, L-
CAS REGISTRY NUMBER :
543-38-4
LAST UPDATED :
199410
DATA ITEMS CITED :
5
MOLECULAR FORMULA :
C5-H12-N4-O3
MOLECULAR WEIGHT :
176.21
WISWESSER LINE NOTATION :
QVYZ2OMYZUM

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LDLo - Lowest published lethal dose
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
7 gm/kg
TOXIC EFFECTS :
Behavioral - altered sleep time (including change in righting reflex) Behavioral - somnolence (general depressed activity)
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Subcutaneous
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
5900 mg/kg
TOXIC EFFECTS :
Behavioral - altered sleep time (including change in righting reflex) Behavioral - muscle contraction or spasticity
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Unreported
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
200 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value

MUTATION DATA

TYPE OF TEST :
DNA inhibition
TEST SYSTEM :
Rodent - hamster Cells - not otherwise specified
DOSE/DURATION :
2200 umol/L
REFERENCE :
JCLLAX Journal of Cellular Physiology. (Alan R. Liss, Inc., 41 E. 11th St., New York, NY 10003) V.67- 1966- Volume(issue)/page/year: 75,129,1970

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H302-H312-H332

[ Precautionary Statements ]:
P280

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xn

[ Risk Phrases ]:
20/21/22

[ RIDADR ]:
NONH for all modes of transport

[ RTECS ]:
ES7002000

[ HS Code ]:
2925290090

Synthetic Route

Precursor & DownStream

Customs

[ 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%

Articles

Rad23 interaction with the proteasome is regulated by phosphorylation of its ubiquitin-like (UbL) domain.

J. Mol. Biol. 426(24) , 4049-60, (2014)

Rad23 was identified as a DNA repair protein, although a role in protein degradation has been described. The protein degradation function of Rad23 contributes to cell cycle progression, stress respons...

Shrimp waste extract and astaxanthin: rat alveolar macrophage, oxidative stress and inflammation.

J. Food Sci. 77(7) , H141-6, (2012)

Astaxanthin is a carotenoid known to have antioxidant and antiinflammatory properties. This study examined if shrimp astaxanthin modulates the production of superoxide (O(-)(2)), nitric oxide (NO), an...

Interactions between phytochemical components of Sutherlandia frutescens and the antiretroviral, atazanavir in vitro: implications for absorption and metabolism.

J. Pharm. Pharm. Sci. 15(2) , 221-33, (2012)

African traditional medicinal plants, such as Sutherlandia frutescens have the potential to interact pharmacokinetically with the protease inhibitor class of antiretrovirals, thereby impacting on thei...


More Articles


Related Compounds