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  • Product Name: BAP9THP
  • Price: $700.0/100mg $1100.0/250mg $2200.0/1g
  • Purity: 98.0%
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2312-73-4

2312-73-4 structure
2312-73-4 structure
  • Name: BAP9THP
  • Chemical Name: N-Benzyl-9-(2-tetrahydropyranyl)adenine
  • CAS Number: 2312-73-4
  • Molecular Formula: C17H19N5O
  • Molecular Weight: 309.366
  • Catalog: Chemical pesticide Plant Growth Regulator
  • Create Date: 2018-04-24 08:00:00
  • Modify Date: 2024-01-06 14:59:38
  • BAP9THP is a synthetic cytokinin derivative and a growth regulator. BAP9THP promotes chlorophyll retention (and senescence delay) in plant tissues exceptionally strongly, and growth of tobacco callus almost as strongly as 6-Benzylaminopurine (BAP). BAP9THP induces adventitious shoot formation ignificantly more strongly than N6-isopentenyladenine or Kinetin[1][2].
Name N-Benzyl-9-(2-tetrahydropyranyl)adenine
Synonyms Pyranyl benzyladenine
MFCD00056971
N-Benzyl-9-(tetrahydro-2H-pyran-2-yl)-9H-purin-6-amine
UNII:23NQ6S177V
9H-Purin-6-amine, N-(phenylmethyl)-9-(tetrahydro-2H-pyran-2-yl)-
N-Benzyl-9-(tetrahydro-2H-pyran-2-yl)adenine
6-Benzylamino-9-(2-tetrahydropyranyl)-9H-purine,BPA
Description BAP9THP is a synthetic cytokinin derivative and a growth regulator. BAP9THP promotes chlorophyll retention (and senescence delay) in plant tissues exceptionally strongly, and growth of tobacco callus almost as strongly as 6-Benzylaminopurine (BAP). BAP9THP induces adventitious shoot formation ignificantly more strongly than N6-isopentenyladenine or Kinetin[1][2].
Related Catalog
In Vitro The cytokinin derivative BAP9THP is an important component of these protocols: culture of isolated apical meristem or growing shoot apices on media containing this compound resulted in signifcant shoot multiplication[1]. both BAP9THP and BAP9THF are found to delay senescence and induce several growth responses more strongly than BAP[2].
References

[1]. Smýkalová, I., et al. The effects of novel synthetic cytokinin derivatives and endogenous cytokinins on the in vitro growth responses of hemp (Cannabis sativa L.) explants. Plant Cell Tiss Organ Cult 139, 381–394 (2019).

[2]. Vylíčilová H, et al. Naturally Occurring and Artificial N9-Cytokinin Conjugates: From Synthesis to Biological Activity and Back. Biomolecules. 2020;10(6):832. Published 2020 May 29.
Density 1.4±0.1 g/cm3
Boiling Point 541.1±60.0 °C at 760 mmHg
Melting Point 110-114ºC
Molecular Formula C17H19N5O
Molecular Weight 309.366
Flash Point 281.1±32.9 °C
Exact Mass 309.158966
PSA 64.86000
LogP 2.45
Vapour Pressure 0.0±1.4 mmHg at 25°C
Index of Refraction 1.700

CHEMICAL IDENTIFICATION

RTECS NUMBER :
UO7510000
CHEMICAL NAME :
9H-Purine, 6-benzylamino-9-tetrahydropyran-2-yl-
CAS REGISTRY NUMBER :
2312-73-4
LAST UPDATED :
199710
DATA ITEMS CITED :
4
MOLECULAR FORMULA :
C17-H19-N5-O
MOLECULAR WEIGHT :
309.41
WISWESSER LINE NOTATION :
T56 BN DN FN HNJ IM1R& D- BT6OTJ

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
1640 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
85ARAE "Agricultural Chemicals," Thomson, W.T., 4 vols., Fresno, CA, Thomson Publications, 1976/77 revision Volume(issue)/page/year: 3,48,1976/1977 ** REPRODUCTIVE DATA **
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Oral
DOSE :
3200 mg/kg
SEX/DURATION :
female 6-15 day(s) after conception
TOXIC EFFECTS :
Reproductive - Effects on Embryo or Fetus - fetotoxicity (except death, e.g., stunted fetus)
REFERENCE :
TOXID9 Toxicologist. (Soc. of Toxicology, Inc., 475 Wolf Ledge Parkway, Akron, OH 44311) V.1- 1981- Volume(issue)/page/year: 1,27,1981 *** U.S. STANDARDS AND REGULATIONS *** EPA FIFRA 1988 PESTICIDE SUBJECT TO REGISTRATION OR RE-REGISTRATION FEREAC Federal Register. (U.S. Government Printing Office, Supt. of Documents, Washington, DC 20402) V.1- 1936- Volume(issue)/page/year: 54,7740,1989
Hazard Codes Xn:Harmful;
Risk Phrases R22
Safety Phrases S26-S36
WGK Germany 3
RTECS UO7510000
7306-68-5 structure

7306-68-5

100-46-9 structure

100-46-9

~23%

2312-73-4 structure

2312-73-4

Literature: Gasque, C. Edward Phytochemistry (Elsevier), 1982 , vol. 21, # 7 p. 1501 - 1508
110-87-2 structure

110-87-2

1214-39-7 structure

1214-39-7

~71%

2312-73-4 structure

2312-73-4

Literature: Villar, Jose Daniel Figueroa; Motta, Marita Almeida Nucleosides, Nucleotides and Nucleic Acids, 2000 , vol. 19, # 5-6 p. 1005 - 1015
19769-32-5 structure

19769-32-5

~%

2312-73-4 structure

2312-73-4

Literature: Nucleosides, Nucleotides and Nucleic Acids, , vol. 19, # 5-6 p. 1005 - 1015
50-66-8 structure

50-66-8

~%

2312-73-4 structure

2312-73-4

Literature: Nucleosides, Nucleotides and Nucleic Acids, , vol. 19, # 5-6 p. 1005 - 1015
100-46-9 structure

100-46-9

~%

2312-73-4 structure

2312-73-4

Literature: Nucleosides, Nucleotides and Nucleic Acids, , vol. 19, # 5-6 p. 1005 - 1015

Chemsrc provides CAS#:2312-73-4 MSDS, density, melting point, boiling point, structure, formula, molecular weight, synthetic route, etc.
title: CAS No. 2312-73-4 | Chemsrc address: https://www.chemsrc.com/en/baike/245719.html

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