Detail of > 716-61-0
- MSDS Download

- CAS Number:
- 716-61-0
- Name:
1,3-Propanediol,2-amino-1-(4-nitrophenyl)-, (1R,2R)-
- Superlist Name:
- (1R,2R)-2-Amino-1-(4-nitrophenyl)propane-1,3-diol
- Formula:
- C9H12N2O4
- Molecular Structure:

- Synonyms:
- 1,3-Propanediol,2-amino-1-(p-nitrophenyl)-, D-threo-(-)- (8CI);(-)-threo-1-(p-Nitrophenyl)-2-amino-1,3-propanediol;(1R,2R)-(-)-2-Amino-1-(4-nitrophenyl)-1,3-propanediol;1,3-Propanediol,2-amino-1-(4-nitrophenyl)-, [R-(R*,R*)]-;(1R,2R)-2-Amino-1-(4-nitrophenyl)-1,3-propanediol;(1R,2R)-threo-(-)-1-(4-Nitrophenyl)-2-amino-1,3-propanediol;Chloramphenicol D base;Chloramphenicol base;D-(-)-threo-1-p-Nitrophenyl-2-amino-1,3-propanediol;D-1-(p-Nitrophenyl)-2-aminopropane-1,3-diol;D-threo-(-)-2-Amino-1-(4-nitrophenyl)-1,3-propanediol;D-threo-(1R,2R)-1-p-Nitrophenyl-2-amino-1,3-propanediol;D-threo-2-Amino-1-(p-nitrophenyl)-1,3-propanediol;
- Molecular Weight:
- 212.10
- EINECS:
- 211-938-7
- Density:
- 1.41 g/cm3
- Melting Point:
- 163-165 °C(lit.)
- Boiling Point:
- 451.9 °C at 760 mmHg
- Flash Point:
- 227.1 °C
- Appearance:
- light yellow powder
- Hazard Symbols:
Xn,
T- Risk Codes:
- 22-36/37/38-45
- Safety:
- 26-45-53Details
- Transport Information:
- UN 3259 8/PG 3
- particular:
- particular
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Reference
- Stimulation of acid phosphatase synthesis and secretion in Ochromonas danica by chloramphenicol base
- Stimulation of acid phosphatase synthesis and secretion in Ochromonas danica by chloramphenicol base. Aaronson, S.; Patni, N. J. (Queens Coll., City Univ. New York, Flushing, N. Y., USA). J. Gen. Microbiol., 104(2), 181-6 (English) 1978. CODEN: JGMIAN. ISSN: 0022-1287. DOCUMENT TYPE: Journal CA Section: 3 (Biochemical Interactions) Secretion of an acid phosphatase [9001-77-8] by a nondividing suspension of O. danica into the medium was stimulated by chloramphenicol base (I) [716-61-0], unaffected by chloramphenicol or mols. resembling it, and inhibited by cycloheximide. I also stimulated total enzyme synthesis. The mechanism of stimulation by I is unknown.
- Disposition and metabolism of chloramphenicol in trout
- Disposition and metabolism of chloramphenicol in trout. Cravedi, J. P.; Heuillet, G.; Peleran, J. C.; Wal, J. M. (Lab. Rech. Addit. Aliment., INRA, Toulouse 31931, Fr.). Xenobiotica, 15(2), 115-21 (English) 1985. CODEN: XENOBH. ISSN: 0049-8254. DOCUMENT TYPE: Journal CA Section: 1 (Pharmacology) The urinary and fecal excretion, tissue distribution, and metab. of 3H-labeled chloramphenicol (CP) [56-75-7] were measured in rainbow trout, Salmo gairdneri, after a single 50 mg/kg intragastric dose. The major route of excretion of 3H was fecal (64.3% of the dose), with ~16% in the urine in 15 days. Radioactivity was widely distributed in trout tissues and organs, the highest concn. being in the bile and intestine. At 48 h after dosing, the radioactivity remaining in the liver, muscle, and perigastric adipose tissue was as CP-derived compds. bound to tissues. In addn. to unchanged CP (4.3% dose after 96 h), the other metabolites excreted in the urine were CP base [716-61-0] (5.2%), CP alc. [23885-72-5] (4.0%), and CP glucuronide [39751-33-2] (1.8%).
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