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Basic information

  • Name:
  • 5'-Uridylic acid,sodium salt (1:2)

  • Superlist Name:
  • Disodium uridine-5'-monophosphate
  • CAS No.:
  • 3387-36-8

  • Molecular Structure:
  • Formula:
  • C9H11N2Na2O9P
  • Molecular Weight:
  • 368.15
  • Synonyms:
  • 5'-Uridylicacid, disodium salt (7CI,8CI,9CI);5'-UMP disodium salt;Disodium 5'-UMP;Disodium 5'-uridylate;Disodium UMP;Disodium uridine 5'-phosphate;NSC 20257;UMP disodium salt;Uridine5'-(dihydrogen phosphate) disodium salt;Uridine 5'-monophosphate disodiumsalt;Uridylic acid disodium salt;
  • EINECS:
  • 222-211-9
  • Melting Point:
  • 208-210 °C
  • Solubility:
  • 40 g/100 mL (20 °C) in water
  • Appearance:
  • Crystalline
  • Hazard Symbols:
  • IrritantXi
  • Risk Codes:
  • 36/37/38
  • Safety Description:
  • 22-24/25-36-26 Details

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Chemistry

IUPAC Name: Disodium [(2R,3S,4S,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methyl phosphate
Systematic of 5'-Uridylic acid,sodium salt (1:2) (CAS NO.3387-36-8): 5'-UMP disodium ; CCRIS 6562 ; Disodium 5'-UMP ; Disodium 5'-uridylate ; Disodium UMP ; Disodium uridine 5'-monophosphate ; Disodium uridine 5'-phosphate ; EINECS 222-211-9 ; NSC 20257 ; Uridine 5'MP, disodium salt ; Uridine-5-monophosphate disodium salt
CAS NO: 3387-36-8
Classification Code: Agricultural Chemical ; Growth regulator / Fertilizer
Molecular Formula of 5'-Uridylic acid,sodium salt (1:2) (CAS NO.3387-36-8): C9H11N2Na2O9P
Molecular Weight: 368.1449
Molecular Structure:

Melting Point: 208-210 °C
Product Categories: Biochemistry ; Nucleosides, Nucleotides & Related Reagents ; Nucleotides and their analogs ; Nucleic acids 
H bond acceptors: 11
H bond donors: 3
Freely Rotating Bonds: 10
Polar Surface Area of 5'-Uridylic acid,sodium salt (1:2) (CAS NO.3387-36-8): 153.67 Å2

Uses

 5'-Uridylic acid,sodium salt (1:2) (CAS NO.3387-36-8) is used as flavoring agent: nucleotide added to the milk to increase volume to make it closer to human milk composition, increase resistance to infants and young children. And it can be used as auxiliary liver disease drug. It also used as production of intermediate nucleic acid drugs asn health food and biochemical reagents. And it for the manufacture of uridine triphosphate (UTP), poly gland urine, drugs such Furtulon.

Toxicity Data With Reference

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
mouse LD50 intraperitoneal 3394mg/kg (3394mg/kg) BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY)

BEHAVIORAL: ATAXIA

LUNGS, THORAX, OR RESPIRATION: CYANOSIS
Toho Igakkai Zasshi. Journal of Medical Society of Toho University. Vol. 22, Pg. 618, 1975.
mouse LD50 oral > 12gm/kg (12000mg/kg) BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY)

LUNGS, THORAX, OR RESPIRATION: DYSPNEA
Toho Igakkai Zasshi. Journal of Medical Society of Toho University. Vol. 22, Pg. 618, 1975.
mouse LD50 subcutaneous 3698mg/kg (3698mg/kg) BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY) Toho Igakkai Zasshi. Journal of Medical Society of Toho University. Vol. 22, Pg. 618, 1975.
rat LD50 intraperitoneal 3111mg/kg (3111mg/kg) BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY)

BEHAVIORAL: ATAXIA

LUNGS, THORAX, OR RESPIRATION: CYANOSIS
Toho Igakkai Zasshi. Journal of Medical Society of Toho University. Vol. 22, Pg. 618, 1975.
rat LD50 oral > 12gm/kg (12000mg/kg)   Toho Igakkai Zasshi. Journal of Medical Society of Toho University. Vol. 22, Pg. 618, 1975.
rat LD50 subcutaneous > 6gm/kg (6000mg/kg) BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY)

SKIN AND APPENDAGES (SKIN): "DERMATITIS, IRRITATIVE: AFTER SYSTEMIC EXPOSURE"
Toho Igakkai Zasshi. Journal of Medical Society of Toho University. Vol. 22, Pg. 618, 1975.

Safety Profile

Hazard Codes: IrritantXi
Risk Statements: 36/37/38 
R36/37/38: Irritating to eyes, respiratory system and skin.
Safety Statements: 22-24/25-36-26 
S22: Do not breathe dust. 
S24/25: Avoid contact with skin and eyes. 
S36: Wear suitable protective clothing. 
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
WGK Germany: 2
RTECS: YU7975000
F: 10-21

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