LINAMARIN
Names
[ CAS No. ]:
554-35-8
[ Name ]:
LINAMARIN
[Synonym ]:
Phaseolunatin
2-methyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropanenitrile
LINAMARIN
Biological Activity
[Description]:
[Related Catalog]:
[References]
Chemical & Physical Properties
[ Density]:
1.41g/cm3
[ Boiling Point ]:
473.3ºC at 760mmHg
[ Melting Point ]:
142-143ºC
[ Molecular Formula ]:
C10H17NO6
[ Molecular Weight ]:
247.24500
[ Flash Point ]:
240ºC
[ Exact Mass ]:
247.10600
[ PSA ]:
123.17000
[ Index of Refraction ]:
1.549
MSDS
Toxicological Information
CHEMICAL IDENTIFICATION
- RTECS NUMBER :
- TZ4850000
- CHEMICAL NAME :
- Propanenitrile, 2-(beta-D-glucopyranosyloxy)-2-methyl-
- CAS REGISTRY NUMBER :
- 554-35-8
- BEILSTEIN REFERENCE NO. :
- 0019237
- LAST UPDATED :
- 199612
- DATA ITEMS CITED :
- 2
- MOLECULAR FORMULA :
- C10-H17-N-O6
- MOLECULAR WEIGHT :
- 247.28
- WISWESSER LINE NOTATION :
- T6OTJ BQ CQ DQ EQ FOX1&1&1CN
HEALTH HAZARD DATA
ACUTE TOXICITY DATA
- TYPE OF TEST :
- LDLo - Lowest published lethal dose
- ROUTE OF EXPOSURE :
- Oral
- SPECIES OBSERVED :
- Rodent - rat
- DOSE/DURATION :
- 500 mg/kg
- TOXIC EFFECTS :
- Sense Organs and Special Senses (Eye) - effect, not otherwise specified Peripheral Nerve and Sensation - flaccid paralysis without anesthesia (usually neuromuscular blockage) Gastrointestinal - hypermotility, diarrhea
- REFERENCE :
- TXAPA9 Toxicology and Applied Pharmacology. (Academic Press, Inc., 1 E. First St., Duluth, MN 55802) V.1- 1959- Volume(issue)/page/year: 42,539,1977 ** REPRODUCTIVE DATA **
- TYPE OF TEST :
- TDLo - Lowest published toxic dose
- ROUTE OF EXPOSURE :
- Oral
- DOSE :
- 120 mg/kg
- SEX/DURATION :
- female 8 day(s) after conception
- TOXIC EFFECTS :
- Reproductive - Specific Developmental Abnormalities - musculoskeletal system
- REFERENCE :
- TJADAB Teratology, The International Journal of Abnormal Development. (Alan R. Liss, Inc., 41 E. 11th St., New York, NY 10003) V.1- 1968- Volume(issue)/page/year: 31,241,1985
Safety Information
[ Symbol ]:
GHS07
[ Signal Word ]:
Warning
[ Hazard Statements ]:
H302-H315-H319-H332-H335
[ Precautionary Statements ]:
P261-P305 + P351 + P338
[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves
[ Hazard Codes ]:
Xn
[ Risk Phrases ]:
20/22-36/37/38
[ RIDADR ]:
NONH for all modes of transport
[ RTECS ]:
TZ4850000
Synthetic Route
Precursor & DownStream
Precursor
DownStream
Articles
J. Food Prot. 78 , 1408-13, (2015)
Consumption of cyanogenic plants can cause serious health problems for humans. The ability to detect and quantify cyanogenic glycosides, capable of generating cyanide, could contribute to prevention o...
A recycling pathway for cyanogenic glycosides evidenced by the comparative metabolic profiling in three cyanogenic plant species.Biochem. J. 469 , 375-89, (2015)
Cyanogenic glycosides are phytoanticipins involved in plant defence against herbivores by virtue of their ability to release toxic hydrogen cyanide (HCN) upon tissue disruption. In addition, endogenou...
Overexpression of hydroxynitrile lyase in cassava roots elevates protein and free amino acids while reducing residual cyanogen levels.PLoS ONE 6(7) , e21996, (2011)
Cassava is the major source of calories for more than 250 million Sub-Saharan Africans, however, it has the lowest protein-to-energy ratio of any major staple food crop in the world. A cassava-based d...