dextro,laevo-citrulline
N5-carbamylornithine
Identification
| Name | dextro,laevo-citrulline |
| IUPAC | 2-amino-5-(carbamoylamino)pentanoic acid |
| CAS Number | 627-77-0 |
| EINECS | 211-012-2 |
| FDA UNII | 1OYO2NV4NM |
| Molecular Formula | C6 H13 N3 O3 |
| Molecular Weight | 175.18821000 |
| MDL Number | MFCD00007955 |
| Nikkaji Number | J3.054.119G |
| Beilstein | 1725417 |
| XlogP3 | -4.30 (est) |
Regulatory
Physical Properties
| Appearance | white powder (est) |
| Assay | 95.00 to 100.00 |
| Food Chemicals Codex Listed | No |
| Boiling Point | 386.00 to 387.00 °C. @ 760.00 mm Hg (est) |
| Flash Point | 370.00 °F. TCC ( 187.70 °C. ) (est) |
| logP (o/w) | -1.373 (est) |
| Soluble in | water, 1.283e+004 mg/L @ 25 °C (est) |
No sensory data available
Safety Information
| Oral/Parenteral Toxicity | Not determined |
| Dermal Toxicity | Not determined |
| Inhalation Toxicity | Not determined |
GHS Classification
['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']
Safety in Use
| Category | information only not used for fragrances or flavors |
| Recommendation for dextro,laevo-citrulline usage levels up to | not for fragrance use. |
| Recommendation for dextro,laevo-citrulline flavor usage levels up to | not for flavor use. |
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Potential Uses
Natural Occurrence
Synonyms
2-
amino-5-(carbamoylamino)pentanoic acid
2-
amino-5-uredovaleric acid
2-
amino-5-ureidopentanoic acid
2-
amino-5-ureidovaleric acid
dextro,laevo-2-
amino-5-ureidovaleric acid
DL-2-
amino-5-ureidovaleric acid
a-
amino-d-ureidovaleric acid
N(5)-(
aminocarbonyl)-DL-ornithine
N5-(
aminocarbonyl)-ornithine
N(5)-(
aminocarbonyl)ornithine
N5-(
aminocarbonyl)ornithine
N(5)-
carbamoyl-DL-ornithine
N(5)-
carbamoylornithine
N5-
carbamoylornithine
N5-
carbamylornithine
DL-
citrulline
gammaureidonorvaline
ornithine, N5-(aminocarbonyl)-
ornithine, N5-carbamoyl-, DL-
PubMed:
Characteristics of a Brucella species from a bottlenose dolphin (Tursiops truncatus).
PubMed:
Incorporation of 14C-labeled compounds into sinefungin (A9145), a nucleoside antifungal antibiotic.
PubMed:
Metabolic characterization of the genus Brucella. II. Oxidative metabolic patterns of the described biotypes.
PubMed:
Metabolic characterization of the genus Brucella. I. Statistical evaluation of the oxidative rates by which type I of each species can be identified.