Z-Gly-OH

Modify Date: 2024-01-02 16:48:20

Z-Gly-OH Structure
Z-Gly-OH structure
Common Name Z-Gly-OH
CAS Number 1138-80-3 Molecular Weight 209.199
Density 1.3±0.1 g/cm3 Boiling Point 424.0±38.0 °C at 760 mmHg
Molecular Formula C10H11NO4 Melting Point 118-122 °C(lit.)
MSDS Chinese USA Flash Point 210.2±26.8 °C

 Use of Z-Gly-OH


Z-Glycine is a Glycine (HY-Y0966) derivative[1].

 Names

Name N-benzyloxycarbonylglycine
Synonym More Synonyms

 Z-Gly-OH Biological Activity

Description Z-Glycine is a Glycine (HY-Y0966) derivative[1].
Related Catalog
In Vitro Amino acids and amino acid derivatives have been commercially used as ergogenic supplements. They influence the secretion of anabolic hormones, supply of fuel during exercise, mental performance during stress related tasks and prevent exercise induced muscle damage. They are recognized to be beneficial as ergogenic dietary substances[1].
References

[1]. Luckose F, et al. Effects of amino acid derivatives on physical, mental, and physiological activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-1144.

 Chemical & Physical Properties

Density 1.3±0.1 g/cm3
Boiling Point 424.0±38.0 °C at 760 mmHg
Melting Point 118-122 °C(lit.)
Molecular Formula C10H11NO4
Molecular Weight 209.199
Flash Point 210.2±26.8 °C
Exact Mass 209.068802
PSA 75.63000
LogP 1.37
Vapour Pressure 0.0±1.1 mmHg at 25°C
Index of Refraction 1.554
Water Solubility methanol: 0.1 g/mL, clear

 Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
MB9129000
CHEMICAL NAME :
Glycine, N-carboxy-, N-benzyl ester
CAS REGISTRY NUMBER :
1138-80-3
BEILSTEIN REFERENCE NO. :
0526877
LAST UPDATED :
199701
DATA ITEMS CITED :
4
MOLECULAR FORMULA :
C10-H11-N-O4
MOLECULAR WEIGHT :
209.22
WISWESSER LINE NOTATION :
QVN1R&1VQ

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intravaginal
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
380 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
JPMSAE Journal of Pharmaceutical Sciences. (American Pharmaceutical Assoc., 2215 Constitution Ave., NW, Washington, DC 20037) V.50- 1961- Volume(issue)/page/year: 68,696,1979 ** REPRODUCTIVE DATA **
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Intraperitoneal
DOSE :
280 mg/kg
SEX/DURATION :
female 28 day(s) after conception
TOXIC EFFECTS :
Reproductive - Fertility - female fertility index (e.g. # females pregnant per # sperm positive females; # females pregnant per # females mated)
REFERENCE :
JPMSAE Journal of Pharmaceutical Sciences. (American Pharmaceutical Assoc., 2215 Constitution Ave., NW, Washington, DC 20037) V.50- 1961- Volume(issue)/page/year: 70,60,1981
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Intravaginal
DOSE :
280 mg/kg
SEX/DURATION :
female 28 day(s) pre-mating
TOXIC EFFECTS :
Reproductive - Fertility - female fertility index (e.g. # females pregnant per # sperm positive females; # females pregnant per # females mated)
REFERENCE :
JPMSAE Journal of Pharmaceutical Sciences. (American Pharmaceutical Assoc., 2215 Constitution Ave., NW, Washington, DC 20037) V.50- 1961- Volume(issue)/page/year: 70,60,1981

 Safety Information

Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xn
Risk Phrases R62
Safety Phrases S24/25
RIDADR NONH for all modes of transport
WGK Germany 3
RTECS MB9129000
HS Code 2924299090

 Synthetic Route

 Customs

HS Code 2924299090
Summary 2924299090. other cyclic amides (including cyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

 Articles4

More Articles
Anticonvulsant activities of N-benzyloxycarbonylglycine after parenteral administration.

Neuroreport 5(7) , 777-80, (1994)

Although glycine does not cross easily the blood-brain barrier, it exhibits at very high doses (10-40 mmol kg-1) a modest anticonvulsant activity. In this study, carbamate derivatives--N-benzyloxycarb...

Substituted hippurates and hippurate analogs as substrates and inhibitors of peptidylglycine alpha-hydroxylating monooxygenase (PHM).

Bioorg. Med. Chem. 16 , 10061-74, (2008)

Peptidyl alpha-hydroxylating monooxygenase (PHM) functions in vivo towards the biosynthesis of alpha-amidated peptide hormones in mammals and insects. PHM is a potential target for the development of ...

Synthesis and anticonvulsant activity of N-benzyloxycarbonyl-amino acid prodrugs of phenytoin.

J. Pharm. Pharmacol. 51 , 549-553, (1999)

Glycine, which has weak anticonvulsant properties, has been shown to potentiate the activity of several antiepileptic drugs but not phenytoin. Recently, studies have shown that N-(benzyloxycarbonyl)gl...

 Synonyms

Cbz-Gly-OH
CBZ-GLYCINE
QV1MVO1R
N-[(Benzyloxy)carbonyl]glycine
N-Carbobenzoxyglycine
Z-GLY-OH
CBZ-GLY
N-Carbobenzyloxyglycine
Z-GLYCINE
Glycine, N-[(phenylmethoxy)carbonyl]-
z-gly
benzyloxycarbonylaminomethylcarboxylic acid
EINECS 214-516-0
MFCD00002691
N-Gly-OH
N-Cbz-glycine
Carbobenzyloxyglycine
{[(Benzyloxy)carbonyl]amino}acetic acid
Benzyloxycarbonylglycine
Benzyloxycarbonyl-glycine
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  • Nanjing Peptide Biotech Ltd
  • China
  • Product Name: Z-Gly-OH
  • Price: ¥Inquiry/10g ¥Inquiry/100g ¥Inquiry/1kg ¥Inquiry/10kg
  • Purity: 98.0%
  • Stocking Period: 7 Day
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