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68-94-0

68-94-0 structure
68-94-0 structure
  • Name: Hypoxanthine
  • Chemical Name: Hypoxanthine
  • CAS Number: 68-94-0
  • Molecular Formula: C5H4N4O
  • Molecular Weight: 136.111
  • Catalog: Biochemical Plant extracts
  • Create Date: 2018-04-05 08:00:00
  • Modify Date: 2026-07-02 18:18:36
  • Hypoxanthine, a purine derivative, is a potential free radical generator and could be used as an indicator of hypoxia.
Name Hypoxanthine
Synonyms 4-Hydroxy-1H-purine
Hypoxsanthine (1,7-Dihydro-6H-purin-6-one)
6H-Purin-6-one, 1,9-dihydro
3,9-Dihydro-6H-purin-6-on
Purin-6(1H)-one
6-Oxopurine
Hypoxanthinee
IFLAB-BB F1386-0269
6H-Purin-6-one, 1,7-dihydro
1H-Purin-6(9H)-one
Azathioprine Impurity F
Hypoxanthine Vetec(TM) ade
Hypexanthine
Hypoxathine
HYPOXANTHINE extrapure
Didanosine Related CoMpound A
6-HYDROXYPURINE(HYPOXANTHINE)
Hypoxanthin
6-Hydroxypurine
HYPOXANTHINE ANHYDROUS
purine-6(1H)-one
6H-Purin-6-one, 1,7-dihydro- (9CI)
Skine
HypoxanthineForBiochemistry
SARKIN
Purine-6-ol
9H-PURIN-6-OL
3H-Purin-6-ol
9H-Purin-6(1H)-one
6-Hydroxy-1H-purine
1,7-Dihydro-6H-purine-6-one
SCINE
Purin-6(3H)-one
6(1H)-PURINONE
1,7-Dihydro-6H-purin-6-on
HYPOXANTHINE CELL CULTURE TESTED
1,7-Dihydro-6H-purin-6-one
HYPOXANTHINE FOR BIOCHEMISTRY
7H-Purin-6-ol
PURIN-6-OL
SARCINE
Hypoxanthine, Animal-Free
hypoxanthineenol
HYPOXANTHINE(RG)
1H-Purin-6(7H)-one
Didanosine Related Compound A (25 mg) (Hypoxanthine)
1,9-Dihydro
Hypoxanthine, R
6-Hydropurine
TTGGTTGGGTGGTHGGTGTTGGGG
3,9-Dihydro-6H-purin-6-one
HYPOXANTHINE
1,7-dihydro-6h-purin-6-on
MFCD00005725
6-oxypurine
Sarkine
3,7-dihydropurin-6-one
TIMTEC-BB SBB004203
HYPOXANTHINE (Hyp)
EINECS 200-697-3
1H,7H-Hypoxanthine
1,7-dihydro-purin-6-one
Hypoxanthine API
Description Hypoxanthine, a purine derivative, is a potential free radical generator and could be used as an indicator of hypoxia.
Related Catalog
Target

Human Endogenous Metabolite

In Vitro Hypoxanthine is a potential free radical generator. Hypoxanthine seems to play a role in posthypoxic reoxygenation cell injury through oxygen radical production and is therefore involved in the pathogenesis of a number of diseases. Hypoxanthine also modulates a number of other processes because it reacts with benzodiazepine receptors and inhibits phosphodiesterase in the brain. Hypoxanthine inhibits the effect of several cytotoxic drugs and may therefore influence treatment with such drugs[1].
In Vivo In pigs, a linear increase of plasma hypoxanthine with duration of hypoxemia is found, and there is no difference between arterial and venous plasma. There are good correlations between hypoxanthine and lactate, base deficit and pH. There is also a direct relationship between survival time and increase in plasma hypoxanthine. Survival time correlates negatively with the rate of hypoxanthine increase (r=-0.62).All animals die when hypoxanthine exceeds 125 pM/liter. The increase of hypoxanthine therefore reflected the prognosis of acute hypoxia in contrast to base deficit[1].
References

[1]. Saugstad OD, et al. Hypoxanthine as an indicator of hypoxia: its role in health and disease through free radical production. Pediatr Res. 1988 Feb;23(2):143-50.
Density 1.7±0.1 g/cm3
Boiling Point 551.0±30.0 °C at 760 mmHg
Melting Point >300 °C(lit.)
Molecular Formula C5H4N4O
Molecular Weight 136.111
Flash Point 287.0±24.6 °C
Exact Mass 136.038513
PSA 74.43000
LogP -0.91
Vapour Pressure 0.0±1.5 mmHg at 25°C
Index of Refraction 1.816
Storage condition 2-8°C
Water Solubility practically insoluble

CHEMICAL IDENTIFICATION

RTECS NUMBER :
UP0791000
CHEMICAL NAME :
6H-Purin-6-one, 1,7-dihydro-
CAS REGISTRY NUMBER :
68-94-0
LAST UPDATED :
199701
DATA ITEMS CITED :
5
MOLECULAR FORMULA :
C5-H4-N4-O
MOLECULAR WEIGHT :
136.13
WISWESSER LINE NOTATION :
T56 BN DM FVM INJ

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
750 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
NTIS** National Technical Information Service. (Springfield, VA 22161) Formerly U.S. Clearinghouse for Scientific & Technical Information. Volume(issue)/page/year: AD691-490 ** REPRODUCTIVE DATA **
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Intraperitoneal
DOSE :
600 mg/kg
SEX/DURATION :
female 13 day(s) after conception
TOXIC EFFECTS :
Reproductive - Effects on Embryo or Fetus - fetotoxicity (except death, e.g., stunted fetus) Reproductive - Effects on Embryo or Fetus - fetal death
REFERENCE :
JJPAAZ Japanese Journal of Pharmacology. (Japanese Pharmacological Soc., c/o Dept. of Pharmacology, Faculty of Medicine, Kyoto Univ., Sakyo-ku, Kyoto 606, Japan) V.1- 1951- Volume(issue)/page/year: 22,201,1972
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Intraperitoneal
DOSE :
1 gm/kg
SEX/DURATION :
female 13 day(s) after conception
TOXIC EFFECTS :
Reproductive - Specific Developmental Abnormalities - craniofacial (including nose and tongue) Reproductive - Specific Developmental Abnormalities - musculoskeletal system
REFERENCE :
JJPAAZ Japanese Journal of Pharmacology. (Japanese Pharmacological Soc., c/o Dept. of Pharmacology, Faculty of Medicine, Kyoto Univ., Sakyo-ku, Kyoto 606, Japan) V.1- 1951- Volume(issue)/page/year: 22,201,1972 *** NIOSH STANDARDS DEVELOPMENT AND SURVEILLANCE DATA *** NIOSH OCCUPATIONAL EXPOSURE SURVEY DATA : NOES - National Occupational Exposure Survey (1983) NOES Hazard Code - X6051 No. of Facilities: 64 (estimated) No. of Industries: 2 No. of Occupations: 5 No. of Employees: 541 (estimated) No. of Female Employees: 355 (estimated)
Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xn:Harmful
Risk Phrases R22;R36/37/38
Safety Phrases S22-S24/25-S37/39-S26
RIDADR NONH for all modes of transport
WGK Germany 3
RTECS UP0791000
HS Code 2933990090
HS Code 2933990090
Summary 2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%
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