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사르코신

사르코신
사르코신 구조식 이미지
카스 번호:
107-97-1
한글명:
사르코신
동의어(한글):
사르코신;사코신
상품명:
Sarcosine
동의어(영문):
Sar;SAR-OH;H-SAR-OH;Sarcosin;SARCOSINE;H-MEGLY-OH;H-SARCOSINE;L-SARCOSINE;N-ME-GLY-OH;CH3NHCH2COOH
CBNumber:
CB9712144
분자식:
C3H7NO2
포뮬러 무게:
89.09
MOL 파일:
107-97-1.mol

사르코신 속성

녹는점
208-212 °C (dec.)(lit.)
끓는 점
165.17°C (rough estimate)
밀도
1.1948 (rough estimate)
굴절률
1.4368 (estimate)
인화점
>100℃
저장 조건
Store at RT.
용해도
H2O: 1 M at 20 °C
산도 계수 (pKa)
2.21(at 25℃)
물리적 상태
Crystals or Powder
색상
Colorless or white to yellow
수소이온지수(pH)
6.1 (100g/l, H2O, 20℃)
수용성
1480 g/L (20 ºC)
감도
Hygroscopic
Merck
14,8373
BRN
1699442
CAS 데이터베이스
107-97-1(CAS DataBase Reference)
NIST
Sarcosine(107-97-1)
EPA
Glycine, N-methyl-(107-97-1)

안전

위험품 표기 Xi
위험 카페고리 넘버 36/37/38
안전지침서 24/25-36-26
WGK 독일 1
RTECS 번호 VQ2897000
F 고인화성물질 3
TSCA Yes
HS 번호 29224995

사르코신 MSDS


H-Sar-OH

사르코신 C화학적 특성, 용도, 생산

화학적 성질

White crystalline powder

용도

Has been found in starfish and sea urchins. It is used as intermediate in the synthesis of antienzyme agents for toothpaste. Found to be a marker for prostate cancer bioagression.

용도

Sarcosine can improve people's intelligence, especially for exams such as the students need to temporarily increase the effectiveness of intelligence is more obvious. sarcosine can increase muscle strength and anaerobic explosiveness.To prevent damage caused by the brain injury. Sarcosine can effectively improve athletic performance,power, and shorten muscle recovery time.

용도

sarcosine is a naturally occurring amino acid that is used in cosmetic formulations as a skin conditioner. There are some studies indicating that it is effective for oily skin. Its chemical name is n-methyl glycine.

정의

ChEBI: A N-alkylglycine that is the N-methyl derivative of glycine. It is an intermediate in the metabolic pathway of glycine.

일반 설명

Deliquescent crystals or powder. Has a sweetish taste.

공기와 물의 반응

Deliquescent. Water soluble.

반응 프로필

Sarcosine is an amide. Amides/imides react with azo and diazo compounds to generate toxic gases. Flammable gases are formed by the reaction of organic amides/imides with strong reducing agents. Amides are very weak bases (weaker than water). Imides are less basic yet and in fact react with strong bases to form salts. That is, they can react as acids. Mixing amides with dehydrating agents such as P2O5 or SOCl2 generates the corresponding nitrile. The combustion of these compounds generates mixed oxides of nitrogen (NOx). Sarcosine is incompatible with acids. .

화재위험

Flash point data for Sarcosine are not available. Sarcosine is probably combustible.

생물학적 활성

Endogenous inhibitor of GlyT1 that displays antipsychotic activity. Potentiates the action of glycine on the NMDA glycine binding site.

Purification Methods

Crystallise sarcosine from absolute EtOH, 95% EtOH or H2O. It sublimes at 180-185o/0.3mm with 99.1% recovery [Gross & Gradsky J Am Chem Soc 77 1678 1955]. [Cocker & Harris J Chem Soc 1291 1940, Cocker & Lapworth J Chem Soc 1897 1931, Greenstein & Winitz The Chemistry of the Amino Acids J. Wiley, Vol 3 p 2750 1961, Beilstein 4 III 1121, 4 IV 2363.]

사르코신 준비 용품 및 원자재

원자재

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