기본 정보
- CAS
1070-89-9- 표준 SMILES
C[Si](C)(C)[N-][Si](C)(C)C.[Na+]- InChIKey
WRIKHQLVHPKCJU-UHFFFAOYSA-N- 분자식
- C6H18NNaSi2
- 평균 분자량
- 183.37 g/mol
- 단동위원소 질량
- 183.08754693
이름 및 식별자
- 우선 이름
- Sodium bis(trimethylsilyl)amide
- IUPAC
- sodium bis(trimethylsilyl)azanide
- 영어명
- Sodium bis(trimethylsilyl)amide
- 분자식
- C6H18NNaSi2
- 분자량
- 183.37
이름 및 동의어
이름 더 보기
데이터베이스 식별자
- CAS
1070-89-9- PubChem CID
- 2724254
- DTXSID
DTXSID5061451- UNII
- X9ZJB79YER
- EC Number
- 213-983-8
- Nikkaji
- J364.613K
물성
구조 계산 물성
- 극성 표면적
- 1 Ų
- 수소 결합 공여자 수
- 0
- 수소 결합 수용자 수
- 1
- 회전 가능 결합 수
- 2
- 무거운 원자 수
- 10
- 형식 전하
- 0
- 복잡도
- 80
실험 및 물리화학적 성질
물리화학적 성질
- 녹는점
- 171 · 171-175 °C (lit.)
- 끓는 점
- 67 °C · 67°C
- 밀도
- 0.904 g/mL · 0.904 g/mL at 25 °C
- 인화점
- 43 °F · 43 °F
- 저장 조건
- 2 · 2-8°C
- 용해도
- 헥산, 톨루엔, 에테르, 테라히드로푸란, 벤젠 및 톨루엔에 용해됩니다.
- 물리적 상태
- 액체
- Specific Gravity
- 0.9 · 0.9
- 색상
- 투명한 주황색에서 갈색까지
- 수용성
- 물과 반응
- BRN
- 3629917 · 3629917
- InChI
- 1S/C6H18NSi2.Na/c1-8(2,3)7-9(4,5)6;/h1-6H3;/q-1;+1
- InChIKey
- WRIKHQLVHPKCJU-UHFFFAOYSA-N
- SMILES
- C[Si](C)(C)N([Na])[Si](C)(C)C
- EPA
- 1 · Silanamine, 1,1,1-trimethyl-N-(trimethylsilyl)-, sodium salt (1070-89-9)
화학적 성질
Slightly yellow to light beige crystalline powder
안전 및 규제
GHS 분류
GHS Classification
Danger
H302 (63.4%): Harmful if swallowed [Warning Acute toxicity, oral];H312 (63.8%): Harmful in contact with skin [Warning Acute toxicity, dermal];H314 (100%): Causes severe skin burns and eye damage [Danger Skin corrosion/irritation];H318 (64.3%): Causes serious eye damage [Danger Serious eye damage/eye irritation];H332 (63.4%): Harmful if inhaled [Warning Acute toxicity, inhalation];H412 (63.8%): Harmful to aquatic life with long lasting effects [Hazardous to the aquatic environment, long-term hazard]
P260, P261, P264, P264+P265, P270, P271, P273, P280, P301+P317, P301+P330+P331, P302+P352, P302+P361+P354, P304+P340, P305+P354+P338, P316, P317, P321, P330, P362+P364, P363, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 235 reports by companies from 11 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.;Information may vary between notifications depending on impurities, additives, and other factors. The percentage value in parenthesis indicates the notified classification ratio from companies that provide hazard codes. Only hazard codes with percentage values above 10% are shown. For more detailed information, please visit ECHA C&L website.
유해성 정보
Regulatory Information
Status: Active Update: 17-11-2022 https://echa.europa.eu/registration-dossier/-/registered-dossier/11731
Silanamine, 1,1,1-trimethyl-N-(trimethylsilyl)-, sodium salt: Does not have an individual approval but may be used under an appropriate group standard
안전 및 보호
Protective Action Criteria (PAC)
30 [mg/m3]
330 [mg/m3]
2000 [mg/m3]
독성 정보
규제 정보
Regulatory Information
Status: Active Update: 17-11-2022 https://echa.europa.eu/registration-dossier/-/registered-dossier/11731
Silanamine, 1,1,1-trimethyl-N-(trimethylsilyl)-, sodium salt: Does not have an individual approval but may be used under an appropriate group standard
안전 데이터
- wgk
- 3
- tsca
- TSCA listed
- ridadr
- UN 3263 8/PG 2
- HS 번호
- 29319090
- risk_code
- 14-34-19-11-67-65-63-48/20-14/15-40-37
- hazard_code
- C,F
- safety_code
- 26-45-62-36/37/39-33-16-43-8
- 포장분류
- III
- 위험 등급
- 4.3
- F 고인화성물질
- 10-21
- Hazard Classifications
- Skin Corr. 1B
- 스토리지 클래스
- 8A - Combustible corrosive hazardous materials
화학 및 산업
용도 및 제조
응용 분야
용도Sodium bis(trimethylsilyl)amide is a synthetically useful reagent in that it combines both high basicity and nucleophilicity, each of which may be exploited for useful organic transformations such as selective formation of enolates, preparation of Wittig reagents, formation of acyl anion equivalents, and the generation of carbenoid species. As a nucleophile, it has been used as a nitrogen source for the preparation of primary amines.It is useful as a sterically hindered base and as a nucleophile.
일반 설명Sodium bis(trimethylsilyl)amide solution (NaHMDS) is widely used as a strong base in organic synthesis for deprotonation reactions and base-catalyzed reactions. It is also involved in the generation of enolates, Wittig reagents and carbenes.
상·하류 제품 정보
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